| geneid | 133060 |
|---|---|
| ensemblid | ENSG00000163982.6 |
| hgncid | 19656 |
| symbol | OTOP1 |
| name | otopetrin 1 |
| refseq_nuc | NM_177998.3 |
| refseq_prot | NP_819056.1 |
| ensembl_nuc | ENST00000296358.5 |
| ensembl_prot | ENSP00000296358.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 4188726 |
| end | 4226929 |
| strand | - |
| ver | v1.2 |
| region | chr4:4188726-4226929 |
| region5000 | chr4:4183726-4231929 |
| regionname0 | OTOP1_chr4_4188726_4226929 |
| regionname5000 | OTOP1_chr4_4183726_4231929 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 612 | 226 | 36 | 38 | 118 | 8 | 26 | 87 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002 | 1/0 | 612 | 119 | 21 | 25 | 63 | 2 | 7 | 53 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0003 | 0/1 | 612 | 17 | 0 | 7 | 6 | 1 | 2 | 5 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0004 | 0/0 | 610 | 12 | 4 | 4 | 0 | 2 | 2 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0005 | 0/0 | 610 | 10 | 0 | 10 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0006 | 0/0 | 612 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0007 | 0/0 | 612 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0008 | 0/0 | 612 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0009 | 0/0 | 610 | 5 | 3 | 0 | 0 | 0 | 2 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0010 | 0/0 | 612 | 4 | 0 | 1 | 0 | 1 | 2 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0011 | 0/0 | 610 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0012 | 0/0 | 612 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0013 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0014 | 0/0 | 610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0015 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0016 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0017 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0018 | 0/0 | 610 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0019 | 0/0 | 612 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1839 | 204 | 35 | 30 | 115 | 7 | 17 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0002 | 1/0 | 1839 | 85 | 5 | 22 | 48 | 2 | 7 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0003 | 0/0 | 1839 | 27 | 10 | 3 | 14 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0004 | 0/0 | 1839 | 22 | 1 | 8 | 3 | 1 | 9 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0005 | 0/1 | 1839 | 17 | 0 | 7 | 6 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0006 | 0/0 | 1833 | 12 | 4 | 4 | 0 | 2 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0007 | 0/0 | 1833 | 10 | 0 | 10 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0008 | 0/0 | 1839 | 8 | 8 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0009 | 0/0 | 1839 | 7 | 7 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0010 | 0/0 | 1839 | 7 | 6 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0011 | 0/0 | 1839 | 4 | 0 | 1 | 0 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0012 | 0/0 | 1833 | 4 | 2 | 0 | 0 | 0 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0013 | 0/0 | 1839 | 4 | 4 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0014 | 0/0 | 1833 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0015 | 0/0 | 1839 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0016 | 0/0 | 1833 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0017 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0018 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0019 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0020 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0021 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0022 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0023 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0024 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0025 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0026 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0027 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| c0028 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| 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 | 1/1 | 143 | 427 | 94 | 86 | 187 | 14 | 44 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| t0002 | 0/0 | 143 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| 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 | 5 | 0 | 0 | 5 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0305 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1839 | 204 | 35 | 30 | 115 | 7 | 17 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0001c0004 | 0/0 | 1839 | 22 | 1 | 8 | 3 | 1 | 9 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0002 | 1/0 | 1839 | 85 | 5 | 22 | 48 | 2 | 7 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0003 | 0/0 | 1839 | 27 | 10 | 3 | 14 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0013 | 0/0 | 1839 | 4 | 4 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0020 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0023 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0028 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0003c0005 | 0/1 | 1839 | 17 | 0 | 7 | 6 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0004c0006 | 0/0 | 1833 | 12 | 4 | 4 | 0 | 2 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0005c0007 | 0/0 | 1833 | 10 | 0 | 10 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0006c0008 | 0/0 | 1839 | 8 | 8 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0007c0010 | 0/0 | 1839 | 7 | 6 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0007c0025 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0008c0009 | 0/0 | 1839 | 7 | 7 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0008c0026 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0009c0012 | 0/0 | 1833 | 4 | 2 | 0 | 0 | 0 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0009c0018 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0010c0011 | 0/0 | 1839 | 4 | 0 | 1 | 0 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0011c0014 | 0/0 | 1833 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0012c0015 | 0/0 | 1839 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0013c0024 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0014c0021 | 0/0 | 1833 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0015c0022 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0016c0019 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0017c0027 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0018c0016 | 0/0 | 1833 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0019c0017 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1981 | 203 | 35 | 30 | 114 | 7 | 17 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0001c0001t0002 | 0/0 | 1981 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0001c0004t0001 | 0/0 | 1981 | 22 | 1 | 8 | 3 | 1 | 9 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0002t0001 | 1/0 | 1981 | 85 | 5 | 22 | 48 | 2 | 7 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0003t0001 | 0/0 | 1981 | 27 | 10 | 3 | 14 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0013t0001 | 0/0 | 1981 | 4 | 4 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0020t0001 | 0/0 | 1981 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0023t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0002c0028t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0003c0005t0001 | 0/1 | 1981 | 17 | 0 | 7 | 6 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0004c0006t0001 | 0/0 | 1975 | 12 | 4 | 4 | 0 | 2 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0005c0007t0001 | 0/0 | 1975 | 10 | 0 | 10 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0006c0008t0001 | 0/0 | 1981 | 8 | 8 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0007c0010t0001 | 0/0 | 1981 | 7 | 6 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0007c0025t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0008c0009t0001 | 0/0 | 1981 | 7 | 7 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0008c0026t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0009c0012t0001 | 0/0 | 1975 | 4 | 2 | 0 | 0 | 0 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0009c0018t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0010c0011t0001 | 0/0 | 1981 | 4 | 0 | 1 | 0 | 1 | 2 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0011c0014t0001 | 0/0 | 1975 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0012c0015t0001 | 0/0 | 1981 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0013c0024t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0014c0021t0001 | 0/0 | 1975 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0015c0022t0001 | 0/0 | 1981 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0016c0019t0001 | 0/0 | 1981 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0017c0027t0001 | 0/0 | 1981 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0018c0016t0001 | 0/0 | 1975 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| a0019c0017t0001 | 0/0 | 1981 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | copy fasta | chr4 | 4183726 | 4231929 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0001c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0305 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0013t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0013t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0013t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0013t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0020t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0023t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0002c0028t0001g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0248 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0003c0005t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0004c0006t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0005c0007t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0005c0007t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0005c0007t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0005c0007t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0005c0007t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0005c0007t0001g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0005c0007t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0005c0007t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0005c0007t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0006c0008t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0006c0008t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0006c0008t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0006c0008t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0006c0008t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0006c0008t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0006c0008t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0006c0008t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0007c0010t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0007c0010t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0007c0010t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0007c0010t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0007c0010t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0007c0010t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0007c0010t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0007c0025t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0008c0009t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0008c0009t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0008c0009t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0008c0009t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0008c0009t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0008c0009t0001g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0008c0009t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0008c0026t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0009c0012t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0009c0012t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0009c0012t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0009c0012t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0009c0018t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0010c0011t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0010c0011t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0010c0011t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0011c0014t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0011c0014t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0012c0015t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0012c0015t0001g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0013c0024t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0014c0021t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0015c0022t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0016c0019t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0017c0027t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0018c0016t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| a0019c0017t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0298 | EUR | GBR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00099 | hp2 | a0004 | c0006 | t0001 | g0058 | EUR | GBR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0243 | EUR | GBR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00280 | hp1 | a0010 | c0011 | t0001 | g0027 | EUR | FIN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00323 | hp2 | a0003 | c0005 | t0001 | g0241 | EUR | FIN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0333 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00544 | hp2 | a0003 | c0005 | t0001 | g0138 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0345 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00609 | hp1 | a0002 | c0003 | t0001 | g0310 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0277 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0257 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00733 | hp1 | a0005 | c0007 | t0001 | g0356 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00738 | hp1 | a0001 | c0004 | t0001 | g0134 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00738 | hp2 | a0003 | c0005 | t0001 | g0271 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG00741 | hp2 | a0001 | c0004 | t0001 | g0278 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0315 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0346 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0318 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01099 | hp2 | a0001 | c0004 | t0001 | g0246 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01106 | hp1 | a0004 | c0006 | t0001 | g0299 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01109 | hp1 | a0007 | c0010 | t0001 | g0379 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0252 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01167 | hp1 | a0002 | c0003 | t0001 | g0097 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01167 | hp2 | a0003 | c0005 | t0001 | g0023 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01168 | hp2 | a0004 | c0006 | t0001 | g0005 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01169 | hp1 | a0003 | c0005 | t0001 | g0023 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01169 | hp2 | a0004 | c0006 | t0001 | g0005 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01175 | hp2 | a0004 | c0006 | t0001 | g0237 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01192 | hp2 | a0003 | c0005 | t0001 | g0230 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0126 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0121 | AMR | PUR | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0186 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01257 | hp2 | a0005 | c0007 | t0001 | g0024 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01258 | hp1 | a0005 | c0007 | t0001 | g0024 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0330 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01261 | hp2 | a0003 | c0005 | t0001 | g0236 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01346 | hp2 | a0010 | c0011 | t0001 | g0027 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0306 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01358 | hp2 | a0001 | c0004 | t0001 | g0287 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01361 | hp1 | a0005 | c0007 | t0001 | g0348 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0316 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01433 | hp1 | a0003 | c0005 | t0001 | g0228 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01433 | hp2 | a0001 | c0004 | t0001 | g0247 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0353 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01891 | hp1 | a0006 | c0008 | t0001 | g0129 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01891 | hp2 | a0011 | c0014 | t0001 | g0366 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01928 | hp2 | a0005 | c0007 | t0001 | g0350 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01943 | hp2 | a0005 | c0007 | t0001 | g0347 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0325 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01975 | hp1 | a0005 | c0007 | t0001 | g0349 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0304 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01978 | hp1 | a0003 | c0005 | t0001 | g0238 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01978 | hp2 | a0005 | c0007 | t0001 | g0351 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0291 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0324 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0136 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0025 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0311 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02145 | hp2 | a0006 | c0008 | t0001 | g0102 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02148 | hp1 | a0005 | c0007 | t0001 | g0045 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | CDX | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02257 | hp1 | a0012 | c0015 | t0001 | g0382 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0109 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0343 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02258 | hp2 | a0007 | c0025 | t0001 | g0375 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02273 | hp2 | a0005 | c0007 | t0001 | g0352 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02280 | hp1 | a0002 | c0003 | t0001 | g0128 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0307 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0344 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0093 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02615 | hp1 | a0002 | c0003 | t0001 | g0189 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02622 | hp1 | a0008 | c0026 | t0001 | g0376 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0096 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02683 | hp1 | a0010 | c0011 | t0001 | g0047 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02683 | hp2 | a0003 | c0005 | t0001 | g0232 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02698 | hp1 | a0001 | c0004 | t0001 | g0060 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02717 | hp1 | a0008 | c0009 | t0001 | g0363 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02717 | hp2 | a0017 | c0027 | t0001 | g0383 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02723 | hp1 | a0006 | c0008 | t0001 | g0103 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02723 | hp2 | a0002 | c0003 | t0001 | g0225 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0300 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02735 | hp2 | a0001 | c0004 | t0001 | g0091 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02809 | hp1 | a0009 | c0018 | t0001 | g0035 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02809 | hp2 | a0008 | c0009 | t0001 | g0378 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0227 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02818 | hp2 | a0002 | c0013 | t0001 | g0101 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02886 | hp1 | a0008 | c0009 | t0001 | g0364 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02895 | hp2 | a0006 | c0008 | t0001 | g0123 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0329 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02896 | hp2 | a0002 | c0003 | t0001 | g0143 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02897 | hp1 | a0006 | c0008 | t0001 | g0127 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0327 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02922 | hp1 | a0007 | c0010 | t0001 | g0369 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02922 | hp2 | a0002 | c0028 | t0001 | g0384 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02965 | hp1 | a0009 | c0012 | t0001 | g0137 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02965 | hp2 | a0004 | c0006 | t0001 | g0124 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02970 | hp2 | a0012 | c0015 | t0001 | g0381 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0319 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03041 | hp2 | a0004 | c0006 | t0001 | g0181 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03098 | hp1 | a0007 | c0010 | t0001 | g0370 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03130 | hp2 | a0002 | c0013 | t0001 | g0226 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0359 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03195 | hp2 | a0002 | c0013 | t0001 | g0122 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03209 | hp1 | a0013 | c0024 | t0001 | g0362 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03239 | hp2 | a0004 | c0006 | t0001 | g0276 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03453 | hp2 | a0006 | c0008 | t0001 | g0098 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03486 | hp1 | a0008 | c0009 | t0001 | g0380 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0361 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03490 | hp2 | a0001 | c0004 | t0001 | g0133 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0044 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0149 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03516 | hp1 | a0007 | c0010 | t0001 | g0374 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0188 | AFR | ESN | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03540 | hp1 | a0008 | c0009 | t0001 | g0377 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0036 | AFR | GWD | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0218 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03654 | hp2 | a0010 | c0011 | t0001 | g0273 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03688 | hp2 | a0016 | c0019 | t0001 | g0328 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03704 | hp1 | a0003 | c0005 | t0001 | g0239 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03710 | hp1 | a0009 | c0012 | t0001 | g0195 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0059 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03927 | hp1 | a0018 | c0016 | t0001 | g0033 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03942 | hp1 | a0019 | c0017 | t0001 | g0034 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03942 | hp2 | a0004 | c0006 | t0001 | g0037 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0317 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04184 | hp1 | a0009 | c0012 | t0001 | g0160 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0107 | SAS | BEB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04204 | hp2 | a0001 | c0004 | t0001 | g0132 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04228 | hp1 | a0001 | c0004 | t0001 | g0231 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0170 | SAS | STU | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18522 | hp2 | a0008 | c0009 | t0001 | g0367 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | CHB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18906 | hp2 | a0001 | c0004 | t0001 | g0190 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18952 | hp2 | a0003 | c0005 | t0001 | g0166 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18965 | hp2 | a0002 | c0020 | t0001 | g0292 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18968 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18969 | hp1 | a0001 | c0004 | t0001 | g0048 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18970 | hp2 | a0002 | c0003 | t0001 | g0200 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18979 | hp2 | a0015 | c0022 | t0001 | g0081 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0309 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18981 | hp2 | a0003 | c0005 | t0001 | g0262 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18988 | hp1 | a0003 | c0005 | t0001 | g0112 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18989 | hp2 | a0001 | c0004 | t0001 | g0040 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18992 | hp2 | a0001 | c0004 | t0001 | g0039 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18999 | hp1 | a0002 | c0003 | t0001 | g0025 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0222 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19012 | hp2 | a0002 | c0003 | t0001 | g0209 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19030 | hp1 | a0002 | c0013 | t0001 | g0100 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19030 | hp2 | a0011 | c0014 | t0001 | g0368 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19043 | hp2 | a0014 | c0021 | t0001 | g0135 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19056 | hp2 | a0002 | c0003 | t0001 | g0258 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19058 | hp1 | a0003 | c0005 | t0001 | g0167 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19066 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19067 | hp1 | a0003 | c0005 | t0001 | g0240 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19070 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19077 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19240 | hp1 | a0007 | c0010 | t0001 | g0372 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA19240 | hp2 | a0006 | c0008 | t0001 | g0099 | AFR | YRI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0183 | AFR | ASW | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0053 | EUR | TSI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA20805 | hp1 | a0004 | c0006 | t0001 | g0005 | EUR | TSI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | TSI | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01123 | hp1 | a0001 | c0004 | t0001 | g0250 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0164 | AMR | CLM | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02109 | hp2 | a0009 | c0012 | t0001 | g0125 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02486 | hp1 | a0004 | c0006 | t0001 | g0275 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02486 | hp2 | a0002 | c0023 | t0001 | g0104 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG02559 | hp2 | a0008 | c0009 | t0001 | g0365 | AFR | ACB | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0115 | AFR | MSL | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG06807 | hp1 | a0004 | c0006 | t0001 | g0274 | AFR | USA | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| HG06807 | hp2 | a0007 | c0010 | t0001 | g0371 | AFR | USA | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA18955 | hp2 | a0002 | c0003 | t0001 | g0217 | EAS | JPT | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA20300 | hp1 | a0007 | c0010 | t0001 | g0373 | AFR | USA | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | USA | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA21309 | hp1 | a0006 | c0008 | t0001 | g0224 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0360 | AFR | LWK | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0005 | t0001 | g0248 | REF | REF | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0305 | REF | REF | OTOP1_chr4_4183726_4231929 | OTOP1 | chr4 | 4183726 | 4231929 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:4197180
|
G | A | 1 | a0005 | 10 | HG00733.hp1 HG01257.hp2 HG01258.hp1 others(7): Show |
missense_variant | MODERATE | c.1654C>T | p.Leu552Phe | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1719/1981 | 1654/1839 | 552/612 | chr4 | 4197180 | ||
| chr4:4197221
|
GCGTTGC | G | 6 | a0004a0005a0009others(3): Show | 31 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
disruptive_inframe_deletion | MODERATE | c.1607_1612delGCAACG | p.Gly536_Asn537del | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1677/1981 | 1607/1839 | 536/612 | chr4 | 4197221 | ||
| chr4:4197356
|
T | G | 1 | a0003 | 17 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(14): Show |
missense_variant | MODERATE | c.1478A>C | p.Lys493Thr | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1543/1981 | 1478/1839 | 493/612 | chr4 | 4197356 | ||
| chr4:4197534
|
C | T | 1 | a0010 | 4 | HG00280.hp1 HG01346.hp2 HG02683.hp1 others(1): Show |
missense_variant | MODERATE | c.1300G>A | p.Val434Met | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1365/1981 | 1300/1839 | 434/612 | chr4 | 4197534 | ||
| chr4:4197638
|
G | C | 1 | a0015 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.1196C>G | p.Ser399Trp | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1261/1981 | 1196/1839 | 399/612 | chr4 | 4197638 | ||
| chr4:4197788
|
A | G | 1 | a0019 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.1046T>C | p.Met349Thr | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1111/1981 | 1046/1839 | 349/612 | chr4 | 4197788 | ||
| chr4:4197907
|
A | T | 10 | a0001a0003a0006others(7): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
missense_variant | MODERATE | c.927T>A | p.Asp309Glu | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 992/1981 | 927/1839 | 309/612 | chr4 | 4197907 | ||
| chr4:4202457
|
T | C | 1 | a0006 | 8 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.721A>G | p.Ile241Val | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 786/1981 | 721/1839 | 241/612 | chr4 | 4202457 | ||
| chr4:4202526
|
C | T | 1 | a0014 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.652G>A | p.Val218Ile | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 717/1981 | 652/1839 | 218/612 | chr4 | 4202526 | ||
| chr4:4202556
|
A | T | 1 | a0016 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.622T>A | p.Phe208Ile | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 687/1981 | 622/1839 | 208/612 | chr4 | 4202556 | ||
| chr4:4226480
|
C | T | 1 | a0017 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.385G>A | p.Gly129Ser | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 450/1981 | 385/1839 | 129/612 | chr4 | 4226480 | ||
| chr4:4226524
|
C | G | 1 | a0018 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.341G>C | p.Ser114Thr | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 406/1981 | 341/1839 | 114/612 | chr4 | 4226524 | ||
| chr4:4226570
|
G | A | 1 | a0013 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.295C>T | p.Leu99Phe | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 360/1981 | 295/1839 | 99/612 | chr4 | 4226570 | ||
| chr4:4226650
|
G | T | 1 | a0019 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.215C>A | p.Ala72Glu | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 280/1981 | 215/1839 | 72/612 | chr4 | 4226650 | ||
| chr4:4226737
|
G | A | 3 | a0007a0008a0011 | 18 | HG01109.hp1 HG01891.hp2 HG02258.hp2 others(15): Show |
missense_variant | MODERATE | c.128C>T | p.Ala43Val | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 193/1981 | 128/1839 | 43/612 | chr4 | 4226737 | ||
| chr4:4226786
|
C | A | 1 | a0012 | 2 | HG02257.hp1 HG02970.hp2 |
missense_variant | MODERATE | c.79G>T | p.Ala27Ser | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 144/1981 | 79/1839 | 27/612 | chr4 | 4226786 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:4197490
|
G | A | 4 | a0002c0013a0002c0023a0007c0025others(1): Show | 7 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(4): Show |
synonymous_variant | LOW | c.1344C>T | p.His448His | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 1409/1981 | 1344/1839 | 448/612 | chr4 | 4197490 | ||
| chr4:4198033
|
G | A | 2 | a0001c0004a0008c0026 | 23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
synonymous_variant | LOW | c.801C>T | p.Ile267Ile | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 866/1981 | 801/1839 | 267/612 | chr4 | 4198033 | ||
| chr4:4198042
|
G | A | 1 | a0002c0020 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.792C>T | p.Ser264Ser | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/6 | 857/1981 | 792/1839 | 264/612 | chr4 | 4198042 | ||
| chr4:4202527
|
G | A | 1 | a0002c0023 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.651C>T | p.Gly217Gly | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 716/1981 | 651/1839 | 217/612 | chr4 | 4202527 | ||
| chr4:4202572
|
T | C | 25 | a0001c0001a0001c0004a0002c0003others(22): Show | 341 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(338): Show |
synonymous_variant | LOW | c.606A>G | p.Gly202Gly | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/6 | 671/1981 | 606/1839 | 202/612 | chr4 | 4202572 | ||
| chr4:4226481
|
C | G | 3 | a0002c0028a0009c0018a0017c0027 | 3 | HG02717.hp2 HG02809.hp1 HG02922.hp2 |
synonymous_variant | LOW | c.384G>C | p.Ala128Ala | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 449/1981 | 384/1839 | 128/612 | chr4 | 4226481 | ||
| chr4:4226736
|
G | T | 1 | a0018c0016 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.129C>A | p.Ala43Ala | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 194/1981 | 129/1839 | 43/612 | chr4 | 4226736 | ||
| chr4:4226859
|
G | A | 2 | a0002c0028a0017c0027 | 2 | HG02717.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.6C>T | p.Leu2Leu | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 71/1981 | 6/1839 | 2/612 | chr4 | 4226859 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:4226915
|
C | G | 1 | a0001c0001t0002 | 1 | NA18993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-51G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/6 | 51 | chr4 | 4226915 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:4189049
|
G | T | 1 | a0008c0009t0001g0367 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1669-76C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189049 | ||||||
| chr4:4189065
|
A | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(285): Show | 321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1669-92T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189065 | ||||||
| chr4:4189120
|
C | T | 1 | a0001c0001t0001g0015 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1669-147G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189120 | ||||||
| chr4:4189184
|
C | A | 28 | a0002c0013t0001g0100a0002c0013t0001g0101a0002c0013t0001g0122others(25): Show | 31 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1669-211G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189184 | ||||||
| chr4:4189187
|
C | G | 22 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(19): Show | 22 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1669-214G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189187 | ||||||
| chr4:4189215
|
A | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 137 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.1669-242T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189215 | ||||||
| chr4:4189368
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(257): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1669-395A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189368 | ||||||
| chr4:4189372
|
C | T | 11 | a0002c0002t0001g0105a0002c0002t0001g0121a0002c0003t0001g0036others(8): Show | 11 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.1669-399G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189372 | ||||||
| chr4:4189511
|
T | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(257): Show | 290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1669-538A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189511 | ||||||
| chr4:4189539
|
C | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(285): Show | 321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1669-566G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189539 | ||||||
| chr4:4189737
|
G | T | 1 | a0002c0003t0001g0126 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1669-764C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189737 | ||||||
| chr4:4189771
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(70): Show | 84 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.1669-798G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189771 | ||||||
| chr4:4189787
|
G | T | 1 | a0002c0002t0001g0131 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1669-814C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4189787 | ||||||
| chr4:4190126
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0233a0002c0002t0001g0044 | 3 | HG03491.hp1 HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1669-1153G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190126 | ||||||
| chr4:4190128
|
C | T | 1 | a0002c0002t0001g0304 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1669-1155G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190128 | ||||||
| chr4:4190164
|
G | C | 93 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(90): Show | 106 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.1669-1191C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190164 | ||||||
| chr4:4190219
|
T | A | 74 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(71): Show | 81 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1669-1246A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190219 | ||||||
| chr4:4190228
|
T | C | 1 | a0001c0004t0001g0149 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1669-1255A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190228 | ||||||
| chr4:4190259
|
G | A | 20 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(17): Show | 20 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1669-1286C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190259 | ||||||
| chr4:4190339
|
C | T | 12 | a0002c0002t0001g0105a0002c0002t0001g0121a0002c0003t0001g0036others(9): Show | 12 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1669-1366G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190339 | ||||||
| chr4:4190405
|
C | T | 4 | a0001c0001t0001g0171a0009c0012t0001g0160a0009c0012t0001g0195others(1): Show | 4 | HG03710.hp1 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669-1432G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190405 | ||||||
| chr4:4190512
|
G | A | 28 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(25): Show | 38 | HG00438.hp1 HG00673.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.1669-1539C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190512 | ||||||
| chr4:4190525
|
G | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(296): Show | 332 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1669-1552C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190525 | ||||||
| chr4:4190721
|
C | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0357a0001c0001t0002g0032 | 3 | HG02083.hp1 NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1669-1748G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190721 | ||||||
| chr4:4190810
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1669-1837C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190810 | ||||||
| chr4:4190869
|
G | C | 1 | a0003c0005t0001g0138 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1669-1896C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190869 | ||||||
| chr4:4190974
|
C | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0069 | 4 | HG02145.hp1 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669-2001G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190974 | ||||||
| chr4:4190979
|
T | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(78): Show | 92 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.1669-2006A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4190979 | ||||||
| chr4:4191102
|
C | T | 56 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(53): Show | 59 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1669-2129G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191102 | ||||||
| chr4:4191105
|
C | G | 12 | a0002c0002t0001g0105a0002c0002t0001g0121a0002c0003t0001g0036others(9): Show | 12 | HG00733.hp2 HG01109.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1669-2132G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191105 | ||||||
| chr4:4191113
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1669-2140G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191113 | ||||||
| chr4:4191177
|
C | T | 3 | a0001c0004t0001g0091a0001c0004t0001g0149a0001c0004t0001g0170 | 3 | HG02735.hp2 HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1669-2204G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191177 | ||||||
| chr4:4191298
|
C | T | 71 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0192others(68): Show | 75 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.1669-2325G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191298 | ||||||
| chr4:4191333
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1669-2360A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191333 | ||||||
| chr4:4191337
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 7 | HG02109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1669-2364G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191337 | ||||||
| chr4:4191482
|
C | T | 2 | a0004c0006t0001g0124a0004c0006t0001g0181 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1669-2509G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191482 | ||||||
| chr4:4191492
|
C | T | 1 | a0007c0010t0001g0369 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1669-2519G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191492 | ||||||
| chr4:4191549
|
C | T | 14 | a0003c0005t0001g0023a0003c0005t0001g0112a0003c0005t0001g0138others(11): Show | 15 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1669-2576G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191549 | ||||||
| chr4:4191612
|
C | T | 1 | a0003c0005t0001g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1669-2639G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191612 | ||||||
| chr4:4191617
|
C | T | 2 | a0001c0004t0001g0149a0001c0004t0001g0170 | 2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1669-2644G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191617 | ||||||
| chr4:4191638
|
A | C | 1 | a0003c0005t0001g0236 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1669-2665T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191638 | ||||||
| chr4:4191640
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0156 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1669-2667G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191640 | ||||||
| chr4:4191650
|
T | C | 53 | a0001c0001t0001g0130a0001c0004t0001g0039a0001c0004t0001g0040others(50): Show | 56 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.1669-2677A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191650 | ||||||
| chr4:4191754
|
T | C | 14 | a0003c0005t0001g0023a0003c0005t0001g0112a0003c0005t0001g0138others(11): Show | 15 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1669-2781A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191754 | ||||||
| chr4:4191789
|
G | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(25): Show | 38 | HG00438.hp1 HG00673.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.1669-2816C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191789 | ||||||
| chr4:4191813
|
G | C | 2 | a0001c0001t0001g0008a0001c0001t0001g0259 | 4 | NA18940.hp2 NA18945.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-2840C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191813 | ||||||
| chr4:4191846
|
C | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(68): Show | 82 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.1669-2873G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4191846 | ||||||
| chr4:4192130
|
T | G | 1 | a0001c0004t0001g0246 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1669-3157A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192130 | ||||||
| chr4:4192172
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1669-3199G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192172 | ||||||
| chr4:4192277
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(83): Show | 97 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.1669-3304G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192277 | ||||||
| chr4:4192309
|
C | T | 2 | a0009c0012t0001g0125a0009c0012t0001g0137 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1669-3336G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192309 | ||||||
| chr4:4192439
|
A | G | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(236): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1669-3466T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192439 | ||||||
| chr4:4192526
|
A | G | 4 | a0001c0001t0001g0171a0009c0012t0001g0160a0009c0012t0001g0195others(1): Show | 4 | HG03710.hp1 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669-3553T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192526 | ||||||
| chr4:4192535
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(231): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1669-3562T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192535 | ||||||
| chr4:4192656
|
A | G | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1669-3683T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192656 | ||||||
| chr4:4192682
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0259 | 4 | NA18940.hp2 NA18945.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1669-3709G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192682 | ||||||
| chr4:4192735
|
C | T | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(250): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1669-3762G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192735 | ||||||
| chr4:4192852
|
G | C | 253 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(250): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1669-3879C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192852 | ||||||
| chr4:4192855
|
T | C | 4 | a0001c0001t0001g0171a0009c0012t0001g0160a0009c0012t0001g0195others(1): Show | 4 | HG03710.hp1 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1669-3882A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192855 | ||||||
| chr4:4192864
|
G | T | 85 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(82): Show | 92 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1669-3891C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192864 | ||||||
| chr4:4192934
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(176): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1669-3961G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192934 | ||||||
| chr4:4192951
|
T | C | 23 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(20): Show | 23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1669-3978A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192951 | ||||||
| chr4:4192980
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.1669-4007G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192980 | ||||||
| chr4:4192995
|
C | T | 383 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(380): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.1669-4022G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4192995 | ||||||
| chr4:4193087
|
C | T | 1 | a0003c0005t0001g0271 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1668+4079G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193087 | ||||||
| chr4:4193126
|
C | T | 2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG02015.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.1668+4040G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193126 | ||||||
| chr4:4193208
|
G | A | 7 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0069others(4): Show | 8 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1668+3958C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193208 | ||||||
| chr4:4193286
|
T | C | 11 | a0001c0001t0001g0130a0001c0001t0001g0193a0006c0008t0001g0098others(8): Show | 11 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1668+3880A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193286 | ||||||
| chr4:4193292
|
A | C | 3 | a0001c0001t0001g0193a0006c0008t0001g0224a0008c0009t0001g0380 | 3 | HG03471.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1668+3874T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193292 | ||||||
| chr4:4193347
|
A | G | 12 | a0001c0001t0001g0130a0001c0001t0001g0193a0006c0008t0001g0098others(9): Show | 12 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1668+3819T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193347 | ||||||
| chr4:4193362
|
G | C | 8 | a0001c0001t0001g0171a0001c0001t0001g0193a0006c0008t0001g0224others(5): Show | 8 | HG02922.hp1 HG03471.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1668+3804C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193362 | ||||||
| chr4:4193417
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1668+3749C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193417 | ||||||
| chr4:4193443
|
T | A | 9 | a0002c0003t0001g0115a0002c0003t0001g0143a0002c0003t0001g0186others(6): Show | 9 | HG01255.hp1 HG02615.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1668+3723A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193443 | ||||||
| chr4:4193554
|
CA | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 246 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1668+3611delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193554 | ||||||
| chr4:4193587
|
C | T | 2 | a0002c0003t0001g0209a0002c0003t0001g0217 | 2 | NA18955.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1668+3579G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193587 | ||||||
| chr4:4193640
|
C | T | 1 | a0002c0002t0001g0311 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1668+3526G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193640 | ||||||
| chr4:4193657
|
C | T | 1 | a0002c0002t0001g0044 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1668+3509G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193657 | ||||||
| chr4:4193673
|
A | G | 48 | a0001c0001t0001g0171a0001c0004t0001g0039a0001c0004t0001g0040others(45): Show | 51 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1668+3493T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193673 | ||||||
| chr4:4193693
|
G | T | 8 | a0002c0013t0001g0100a0002c0013t0001g0101a0002c0013t0001g0122others(5): Show | 8 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1668+3473C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193693 | ||||||
| chr4:4193809
|
G | T | 2 | a0009c0012t0001g0125a0009c0012t0001g0137 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1668+3357C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193809 | ||||||
| chr4:4193856
|
G | A | 1 | a0003c0005t0001g0230 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1668+3310C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193856 | ||||||
| chr4:4193897
|
A | AG | 21 | a0004c0006t0001g0005a0004c0006t0001g0037a0004c0006t0001g0058others(18): Show | 24 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1668+3268_1668+326 others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193897 | ||||||
| chr4:4193916
|
G | A | 1 | a0001c0004t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1668+3250C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193916 | ||||||
| chr4:4193929
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(197): Show | 227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.1668+3237G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193929 | ||||||
| chr4:4193930
|
G | A | 1 | a0002c0020t0001g0292 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1668+3236C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4193930 | ||||||
| chr4:4194013
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1668+3153G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194013 | ||||||
| chr4:4194014
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG02056.hp2 NA18966.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1668+3152G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194014 | ||||||
| chr4:4194081
|
C | T | 23 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(20): Show | 23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1668+3085G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194081 | ||||||
| chr4:4194138
|
A | G | 2 | a0009c0012t0001g0125a0009c0012t0001g0137 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1668+3028T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194138 | ||||||
| chr4:4194158
|
C | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(275): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1668+3008G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194158 | ||||||
| chr4:4194244
|
A | C | 19 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(16): Show | 22 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1668+2922T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194244 | ||||||
| chr4:4194301
|
C | G | 27 | a0001c0001t0001g0171a0001c0004t0001g0039a0001c0004t0001g0040others(24): Show | 27 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1668+2865G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194301 | ||||||
| chr4:4194315
|
C | T | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(271): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1668+2851G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194315 | ||||||
| chr4:4194318
|
A | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(271): Show | 307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.1668+2848T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194318 | ||||||
| chr4:4194359
|
C | T | 1 | a0002c0013t0001g0122 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1668+2807G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194359 | ||||||
| chr4:4194486
|
T | C | 1 | a0001c0004t0001g0277 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1668+2680A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194486 | ||||||
| chr4:4194509
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1668+2657C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194509 | ||||||
| chr4:4194636
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1668+2530A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194636 | ||||||
| chr4:4194656
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1668+2510C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194656 | ||||||
| chr4:4194658
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1668+2508G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194658 | ||||||
| chr4:4194699
|
G | C | 1 | a0007c0010t0001g0369 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1668+2467C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194699 | ||||||
| chr4:4194719
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1668+2447T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194719 | ||||||
| chr4:4194750
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1668+2416C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194750 | ||||||
| chr4:4194766
|
G | A | 1 | a0007c0010t0001g0369 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1668+2400C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194766 | ||||||
| chr4:4194814
|
G | T | 3 | a0010c0011t0001g0027a0010c0011t0001g0047a0010c0011t0001g0273 | 4 | HG00280.hp1 HG01346.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668+2352C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194814 | ||||||
| chr4:4194835
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(212): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1668+2331G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4194835 | ||||||
| chr4:4195038
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(221): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1668+2128A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195038 | ||||||
| chr4:4195076
|
A | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(213): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1668+2090T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195076 | ||||||
| chr4:4195228
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1668+1938C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195228 | ||||||
| chr4:4195254
|
C | G | 2 | a0001c0001t0001g0251a0001c0001t0001g0272 | 2 | HG02135.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1668+1912G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195254 | ||||||
| chr4:4195349
|
T | C | 8 | a0002c0003t0001g0036a0002c0003t0001g0126a0002c0003t0001g0128others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1668+1817A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195349 | ||||||
| chr4:4195562
|
G | A | 7 | a0002c0013t0001g0100a0002c0013t0001g0101a0002c0013t0001g0122others(4): Show | 7 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1668+1604C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195562 | ||||||
| chr4:4195649
|
A | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(295): Show | 331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.1668+1517T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195649 | ||||||
| chr4:4195710
|
A | T | 1 | a0001c0001t0001g0249 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1668+1456T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195710 | ||||||
| chr4:4195897
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(188): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1668+1269C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195897 | ||||||
| chr4:4195926
|
T | C | 26 | a0001c0001t0001g0193a0001c0004t0001g0039a0001c0004t0001g0040others(23): Show | 26 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1668+1240A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4195926 | ||||||
| chr4:4196171
|
C | T | 1 | a0005c0007t0001g0349 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1668+995G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196171 | ||||||
| chr4:4196177
|
G | T | 3 | a0010c0011t0001g0027a0010c0011t0001g0047a0010c0011t0001g0273 | 4 | HG00280.hp1 HG01346.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1668+989C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196177 | ||||||
| chr4:4196186
|
A | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(153): Show | 180 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1668+980T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196186 | ||||||
| chr4:4196349
|
C | T | 16 | a0003c0005t0001g0023a0003c0005t0001g0112a0003c0005t0001g0138others(13): Show | 17 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1668+817G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196349 | ||||||
| chr4:4196350
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0206a0001c0001t0001g0220 | 3 | HG02129.hp2 NA18944.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1668+816C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196350 | ||||||
| chr4:4196469
|
A | G | 1 | a0002c0002t0001g0358 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1668+697T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196469 | ||||||
| chr4:4196481
|
C | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0049others(10): Show | 15 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1668+685G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196481 | ||||||
| chr4:4196507
|
A | G | 16 | a0003c0005t0001g0023a0003c0005t0001g0112a0003c0005t0001g0138others(13): Show | 17 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1668+659T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196507 | ||||||
| chr4:4196678
|
T | G | 1 | a0001c0001t0001g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1668+488A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196678 | ||||||
| chr4:4196764
|
C | T | 5 | a0002c0003t0001g0126a0002c0003t0001g0128a0002c0003t0001g0188others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1668+402G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196764 | ||||||
| chr4:4196857
|
C | G | 10 | a0002c0013t0001g0100a0002c0013t0001g0101a0002c0013t0001g0122others(7): Show | 10 | HG02258.hp2 HG02486.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1668+309G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4196857 | ||||||
| chr4:4197088
|
C | G | 19 | a0001c0001t0001g0177a0001c0001t0001g0233a0003c0005t0001g0023others(16): Show | 20 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1668+78G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4197088 | ||||||
| chr4:4197089
|
T | C | 1 | a0007c0010t0001g0374 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1668+77A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4197089 | ||||||
| chr4:4197124
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1668+42T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4197124 | ||||||
| chr4:4197154
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1668+12C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 5/5 | chr4 | 4197154 | ||||||
| chr4:4198232
|
G | A | 1 | a0002c0002t0001g0316 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.731-129C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198232 | ||||||
| chr4:4198254
|
A | G | 43 | a0002c0003t0001g0036a0002c0003t0001g0096a0002c0003t0001g0097others(40): Show | 46 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.731-151T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198254 | ||||||
| chr4:4198270
|
T | C | 1 | a0002c0003t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.731-167A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198270 | ||||||
| chr4:4198359
|
T | C | 2 | a0008c0009t0001g0377a0008c0009t0001g0378 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.731-256A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198359 | ||||||
| chr4:4198373
|
A | T | 60 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(57): Show | 66 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.731-270T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198373 | ||||||
| chr4:4198384
|
T | TGATA | 17 | a0001c0001t0001g0233a0003c0005t0001g0023a0003c0005t0001g0112others(14): Show | 18 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.731-285_731-282dup others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198384 | ||||||
| chr4:4198492
|
T | C | 17 | a0001c0001t0001g0233a0003c0005t0001g0023a0003c0005t0001g0112others(14): Show | 18 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.731-389A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198492 | ||||||
| chr4:4198527
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.731-424T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198527 | ||||||
| chr4:4198560
|
A | G | 85 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(82): Show | 96 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.731-457T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198560 | ||||||
| chr4:4198659
|
G | A | 42 | a0002c0003t0001g0036a0002c0003t0001g0109a0002c0003t0001g0126others(39): Show | 45 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.731-556C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198659 | ||||||
| chr4:4198684
|
G | T | 1 | a0002c0002t0001g0009 | 3 | HG01069.hp1 HG01071.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.731-581C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198684 | ||||||
| chr4:4198740
|
G | A | 2 | a0001c0001t0001g0339a0002c0002t0001g0053 | 2 | NA19088.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.731-637C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198740 | ||||||
| chr4:4198894
|
C | A | 1 | a0002c0002t0001g0105 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.731-791G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198894 | ||||||
| chr4:4198919
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0192others(9): Show | 13 | HG02109.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.731-816C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4198919 | ||||||
| chr4:4199059
|
C | T | 9 | a0002c0003t0001g0096a0002c0003t0001g0097a0002c0013t0001g0100others(6): Show | 9 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.731-956G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199059 | ||||||
| chr4:4199125
|
G | A | 1 | a0004c0006t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.731-1022C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199125 | ||||||
| chr4:4199220
|
T | TTGTGTG | 5 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 6 | HG02109.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1123_731-1118d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | ||||||
| chr4:4199220
|
T | TTGTGTGT others(1): Show |
23 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(20): Show | 31 | HG00735.hp2 HG01069.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.731-1125_731-1118d others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | ||||||
| chr4:4199220
|
T | TTGTGTGT others(3): Show |
25 | a0001c0001t0001g0161a0001c0001t0001g0233a0001c0004t0001g0132others(22): Show | 27 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.731-1127_731-1118d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | ||||||
| chr4:4199220
|
T | TTGTGTGT others(5): Show |
96 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(93): Show | 102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.731-1129_731-1118d others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | ||||||
| chr4:4199220
|
T | TTGTGTGT others(7): Show |
25 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0092others(22): Show | 25 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.731-1131_731-1118d others(16): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | ||||||
| chr4:4199220
|
T | TTGTGTGT others(9): Show |
6 | a0001c0001t0001g0038a0001c0001t0001g0145a0001c0004t0001g0040others(3): Show | 6 | HG00140.hp1 HG01433.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1118_731-1117i others(18): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | ||||||
| chr4:4199220
|
T | TTGTGTGT others(11): Show |
3 | a0001c0001t0001g0057a0001c0004t0001g0048a0001c0004t0001g0060 | 3 | HG02698.hp1 NA18967.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.731-1118_731-1117i others(20): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199220 | ||||||
| chr4:4199233
|
T | TGA | 23 | a0002c0002t0001g0009a0002c0002t0001g0029a0002c0002t0001g0090others(20): Show | 26 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.731-1132_731-1131d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | ||||||
| chr4:4199233
|
T | TGAGA | 15 | a0002c0002t0001g0202a0002c0002t0001g0215a0002c0002t0001g0253others(12): Show | 15 | HG00544.hp1 HG01192.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.731-1134_731-1131d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | ||||||
| chr4:4199233
|
T | TGAGAGAG others(3): Show |
4 | a0002c0002t0001g0093a0002c0003t0001g0109a0002c0028t0001g0384others(1): Show | 4 | HG02257.hp2 HG02602.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-1140_731-1131d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | ||||||
| chr4:4199233
|
T | TGAGAGAG others(5): Show |
1 | a0008c0009t0001g0378 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.731-1142_731-1131d others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | ||||||
| chr4:4199233
|
TGA | T | 5 | a0002c0002t0001g0031a0002c0002t0001g0055a0002c0002t0001g0314others(2): Show | 6 | HG02818.hp1 NA18959.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.731-1132_731-1131d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | ||||||
| chr4:4199233
|
TGAGA | T | 3 | a0002c0002t0001g0054a0005c0007t0001g0024a0013c0024t0001g0362 | 4 | HG01257.hp2 HG01258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-1134_731-1131d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | ||||||
| chr4:4199233
|
TGAGAGA | T | 7 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0085others(4): Show | 7 | HG00099.hp2 HG01928.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.731-1136_731-1131d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | ||||||
| chr4:4199233
|
TGAGAGAG others(1): Show |
T | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(60): Show | 76 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.731-1138_731-1131d others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199233 | ||||||
| chr4:4199235
|
A | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(181): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.731-1132T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199235 | ||||||
| chr4:4199237
|
A | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(180): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.731-1134T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199237 | ||||||
| chr4:4199239
|
A | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(179): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.731-1136T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199239 | ||||||
| chr4:4199241
|
A | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(168): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.731-1138T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199241 | ||||||
| chr4:4199243
|
A | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 187 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.731-1140T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199243 | ||||||
| chr4:4199245
|
A | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0015others(63): Show | 76 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.731-1142T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199245 | ||||||
| chr4:4199247
|
A | T | 49 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(46): Show | 55 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.731-1144T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199247 | ||||||
| chr4:4199249
|
A | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0192others(7): Show | 11 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.731-1146T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199249 | ||||||
| chr4:4199251
|
A | T | 7 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 8 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-1148T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199251 | ||||||
| chr4:4199253
|
A | T | 1 | a0001c0001t0001g0355 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.731-1150T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199253 | ||||||
| chr4:4199295
|
C | T | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.731-1192G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199295 | ||||||
| chr4:4199378
|
C | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(180): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.731-1275G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199378 | ||||||
| chr4:4199389
|
G | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(180): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.731-1286C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199389 | ||||||
| chr4:4199490
|
T | G | 1 | a0002c0002t0001g0266 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.731-1387A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199490 | ||||||
| chr4:4199552
|
A | G | 17 | a0001c0001t0001g0233a0003c0005t0001g0023a0003c0005t0001g0112others(14): Show | 18 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.731-1449T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199552 | ||||||
| chr4:4199560
|
G | A | 1 | a0001c0004t0001g0048 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.731-1457C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199560 | ||||||
| chr4:4199566
|
C | T | 18 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 21 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.731-1463G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199566 | ||||||
| chr4:4199570
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(180): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.731-1467C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199570 | ||||||
| chr4:4199586
|
C | A | 23 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(20): Show | 23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.731-1483G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199586 | ||||||
| chr4:4199615
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(180): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.731-1512C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199615 | ||||||
| chr4:4199655
|
C | T | 1 | a0012c0015t0001g0382 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.731-1552G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199655 | ||||||
| chr4:4199656
|
G | A | 23 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(20): Show | 23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.731-1553C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199656 | ||||||
| chr4:4199709
|
G | A | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.731-1606C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199709 | ||||||
| chr4:4199838
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(206): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.731-1735C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199838 | ||||||
| chr4:4199852
|
T | C | 1 | a0002c0002t0001g0302 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.731-1749A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199852 | ||||||
| chr4:4199980
|
A | T | 1 | a0001c0001t0001g0284 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.731-1877T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4199980 | ||||||
| chr4:4200018
|
C | T | 26 | a0002c0003t0001g0109a0002c0028t0001g0384a0004c0006t0001g0005others(23): Show | 29 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.731-1915G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200018 | ||||||
| chr4:4200154
|
C | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(81): Show | 94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.731-2051G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200154 | ||||||
| chr4:4200165
|
T | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(207): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.731-2062A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200165 | ||||||
| chr4:4200197
|
T | TA | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.731-2095dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200197 | ||||||
| chr4:4200222
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0326 | 3 | HG01517.hp1 HG02300.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.731-2119C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200222 | ||||||
| chr4:4200233
|
C | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(80): Show | 102 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.731-2130G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200233 | ||||||
| chr4:4200335
|
C | G | 1 | a0001c0001t0001g0207 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.730+2113G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200335 | ||||||
| chr4:4200401
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0256 | 2 | HG02155.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.730+2047C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200401 | ||||||
| chr4:4200425
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.730+2023C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200425 | ||||||
| chr4:4200434
|
C | T | 2 | a0002c0002t0001g0030a0002c0002t0001g0295 | 3 | NA18943.hp1 NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.730+2014G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200434 | ||||||
| chr4:4200473
|
T | TA | 198 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(195): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.730+1974dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200473 | ||||||
| chr4:4200473
|
T | TAA | 13 | a0001c0001t0001g0038a0001c0001t0001g0066a0001c0001t0001g0193others(10): Show | 13 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.730+1973_730+1974d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200473 | ||||||
| chr4:4200504
|
A | G | 23 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(20): Show | 23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.730+1944T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200504 | ||||||
| chr4:4200590
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.730+1858C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200590 | ||||||
| chr4:4200623
|
A | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(169): Show | 188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.730+1825T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200623 | ||||||
| chr4:4200662
|
A | T | 176 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(173): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.730+1786T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200662 | ||||||
| chr4:4200723
|
C | CT | 104 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(101): Show | 123 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.730+1724dupA | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | ||||||
| chr4:4200723
|
C | CTT | 27 | a0001c0001t0001g0194a0002c0003t0001g0109a0002c0028t0001g0384others(24): Show | 30 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.730+1723_730+1724d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | ||||||
| chr4:4200723
|
C | CTTT | 55 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(52): Show | 60 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.730+1722_730+1724d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | ||||||
| chr4:4200723
|
C | CTTTT | 108 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(105): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.730+1721_730+1724d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | ||||||
| chr4:4200723
|
C | CTTTTT | 9 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG00280.hp2 HG00642.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+1720_730+1724d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200723 | ||||||
| chr4:4200810
|
G | A | 16 | a0002c0003t0001g0036a0002c0003t0001g0126a0002c0003t0001g0128others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.730+1638C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200810 | ||||||
| chr4:4200810
|
G | T | 1 | a0001c0001t0001g0004 | 3 | NA18944.hp1 NA18948.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.730+1638C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200810 | ||||||
| chr4:4200873
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(206): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.730+1575T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200873 | ||||||
| chr4:4200905
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.730+1543G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200905 | ||||||
| chr4:4200906
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0001g0213 | 2 | HG03669.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.730+1542C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200906 | ||||||
| chr4:4200966
|
A | G | 18 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 21 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.730+1482T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200966 | ||||||
| chr4:4200967
|
G | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(206): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.730+1481C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4200967 | ||||||
| chr4:4201004
|
C | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 6 | HG02109.hp1 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+1444G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201004 | ||||||
| chr4:4201074
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(90): Show | 111 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.730+1374C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201074 | ||||||
| chr4:4201093
|
T | C | 112 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(109): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.730+1355A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201093 | ||||||
| chr4:4201097
|
C | T | 10 | a0001c0001t0001g0193a0006c0008t0001g0098a0006c0008t0001g0099others(7): Show | 10 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.730+1351G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201097 | ||||||
| chr4:4201294
|
G | A | 4 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137others(1): Show | 4 | HG02109.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+1154C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201294 | ||||||
| chr4:4201363
|
G | A | 18 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(15): Show | 21 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.730+1085C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201363 | ||||||
| chr4:4201435
|
T | A | 3 | a0009c0012t0001g0125a0009c0012t0001g0137a0012c0015t0001g0381 | 3 | HG02109.hp2 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.730+1013A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201435 | ||||||
| chr4:4201459
|
AAT | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 8 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.730+987_730+988del others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201459 | ||||||
| chr4:4201463
|
T | TAC | 15 | a0004c0006t0001g0005a0004c0006t0001g0058a0004c0006t0001g0237others(12): Show | 18 | HG00099.hp2 HG00733.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.730+984_730+985ins others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201463 | ||||||
| chr4:4201463
|
T | TACACAC | 5 | a0002c0003t0001g0109a0004c0006t0001g0299a0008c0009t0001g0377others(2): Show | 5 | HG01106.hp1 HG02257.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.730+984_730+985ins others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201463 | ||||||
| chr4:4201463
|
T | TACACACA others(1): Show |
4 | a0004c0006t0001g0124a0004c0006t0001g0181a0008c0009t0001g0378others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+984_730+985ins others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201463 | ||||||
| chr4:4201465
|
T | C | 26 | a0002c0003t0001g0109a0002c0028t0001g0384a0004c0006t0001g0005others(23): Show | 29 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.730+983A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201465 | ||||||
| chr4:4201465
|
T | TACACACA others(5): Show |
2 | a0006c0008t0001g0123a0006c0008t0001g0127 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.730+982_730+983ins others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201465 | ||||||
| chr4:4201467
|
T | C | 31 | a0001c0001t0001g0193a0001c0001t0001g0267a0001c0001t0001g0269others(28): Show | 34 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.730+981A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | ||||||
| chr4:4201467
|
T | TAC | 31 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0038others(28): Show | 34 | HG00280.hp1 HG00621.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | ||||||
| chr4:4201467
|
T | TACAC | 4 | a0001c0001t0001g0268a0002c0003t0001g0209a0002c0003t0001g0217others(1): Show | 4 | HG02970.hp2 NA18955.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | ||||||
| chr4:4201467
|
T | TACACACA others(1): Show |
7 | a0001c0004t0001g0048a0006c0008t0001g0099a0006c0008t0001g0102others(4): Show | 7 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | ||||||
| chr4:4201467
|
T | TACACACA others(3): Show |
6 | a0001c0004t0001g0059a0001c0004t0001g0060a0001c0004t0001g0246others(3): Show | 6 | HG01099.hp2 HG01123.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | ||||||
| chr4:4201467
|
T | TACACACA others(5): Show |
16 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0091others(13): Show | 16 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.730+980_730+981ins others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201467 | ||||||
| chr4:4201469
|
T | C | 100 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0038others(97): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.730+979A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | ||||||
| chr4:4201469
|
T | TAC | 41 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0016others(38): Show | 49 | HG00323.hp1 HG00438.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.730+978_730+979ins others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | ||||||
| chr4:4201469
|
T | TACAC | 3 | a0001c0001t0001g0263a0001c0001t0001g0360a0009c0012t0001g0125 | 3 | HG02109.hp2 HG02698.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.730+978_730+979ins others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | ||||||
| chr4:4201469
|
T | TACACAC | 6 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG00280.hp2 HG00642.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+978_730+979ins others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | ||||||
| chr4:4201469
|
T | TACACACA others(1): Show |
4 | a0001c0001t0001g0233a0002c0003t0001g0096a0003c0005t0001g0232others(1): Show | 4 | HG02630.hp1 HG02683.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.730+978_730+979ins others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | ||||||
| chr4:4201469
|
T | TACACACA others(3): Show |
2 | a0002c0013t0001g0101a0017c0027t0001g0383 | 2 | HG02717.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.730+978_730+979ins others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | ||||||
| chr4:4201469
|
T | TACACACA others(5): Show |
5 | a0002c0003t0001g0097a0002c0013t0001g0100a0002c0013t0001g0226others(2): Show | 5 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+978_730+979ins others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | ||||||
| chr4:4201469
|
T | TACACACA others(7): Show |
1 | a0002c0013t0001g0122 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.730+978_730+979ins others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201469 | ||||||
| chr4:4201471
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(240): Show | 277 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.730+977A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | ||||||
| chr4:4201471
|
T | TAC | 21 | a0001c0001t0001g0144a0001c0001t0001g0159a0001c0001t0001g0242others(18): Show | 21 | HG00140.hp2 HG01070.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.730+975_730+976dup others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | ||||||
| chr4:4201471
|
T | TACACACA others(1): Show |
14 | a0001c0001t0001g0020a0003c0005t0001g0023a0003c0005t0001g0112others(11): Show | 16 | HG00323.hp2 HG00544.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.730+969_730+976dup others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | ||||||
| chr4:4201471
|
T | TACACACA others(3): Show |
2 | a0003c0005t0001g0238a0008c0009t0001g0367 | 2 | HG01978.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.730+967_730+976dup others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | ||||||
| chr4:4201471
|
T | TATATATA others(3): Show |
1 | a0009c0012t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.730+976_730+977ins others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201471 | ||||||
| chr4:4201473
|
C | T | 1 | a0002c0002t0001g0093 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.730+975G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201473 | ||||||
| chr4:4201501
|
T | C | 9 | a0002c0003t0001g0096a0002c0003t0001g0097a0002c0013t0001g0100others(6): Show | 9 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+947A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201501 | ||||||
| chr4:4201515
|
T | A | 2 | a0008c0009t0001g0363a0012c0015t0001g0381 | 2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.730+933A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201515 | ||||||
| chr4:4201597
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.730+851G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201597 | ||||||
| chr4:4201690
|
A | G | 1 | a0002c0002t0001g0346 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.730+758T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201690 | ||||||
| chr4:4201893
|
A | C | 27 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(24): Show | 31 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.730+555T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201893 | ||||||
| chr4:4201951
|
G | A | 9 | a0002c0003t0001g0096a0002c0003t0001g0097a0002c0013t0001g0100others(6): Show | 9 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+497C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4201951 | ||||||
| chr4:4202013
|
A | G | 1 | a0002c0002t0001g0218 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.730+435T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202013 | ||||||
| chr4:4202163
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(300): Show | 341 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.730+285A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202163 | ||||||
| chr4:4202207
|
C | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0088a0001c0001t0001g0288others(1): Show | 5 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.730+241G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202207 | ||||||
| chr4:4202248
|
A | T | 1 | a0009c0018t0001g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.730+200T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202248 | ||||||
| chr4:4202262
|
A | T | 1 | a0001c0001t0001g0270 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.730+186T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202262 | ||||||
| chr4:4202275
|
G | A | 1 | a0009c0018t0001g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.730+173C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202275 | ||||||
| chr4:4202308
|
CG | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 8 | HG02109.hp1 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.730+139delC | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202308 | ||||||
| chr4:4202309
|
G | A | 8 | a0006c0008t0001g0098a0006c0008t0001g0099a0006c0008t0001g0102others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+139C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202309 | ||||||
| chr4:4202343
|
G | A | 9 | a0002c0003t0001g0096a0002c0003t0001g0097a0002c0013t0001g0100others(6): Show | 9 | HG01167.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+105C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202343 | ||||||
| chr4:4202396
|
T | C | 1 | a0009c0018t0001g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.730+52A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 4/5 | chr4 | 4202396 | ||||||
| chr4:4202622
|
C | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0152 | 4 | NA18939.hp1 NA18970.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-44G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202622 | ||||||
| chr4:4202649
|
G | A | 1 | a0009c0018t0001g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.600-71C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202649 | ||||||
| chr4:4202852
|
G | A | 1 | a0003c0005t0001g0232 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.600-274C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202852 | ||||||
| chr4:4202976
|
A | C | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.600-398T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202976 | ||||||
| chr4:4202986
|
T | C | 1 | a0001c0001t0001g0057 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.600-408A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4202986 | ||||||
| chr4:4203114
|
C | T | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.600-536G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203114 | ||||||
| chr4:4203379
|
G | A | 22 | a0002c0003t0001g0109a0002c0028t0001g0384a0004c0006t0001g0005others(19): Show | 25 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.600-801C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203379 | ||||||
| chr4:4203403
|
A | G | 2 | a0008c0009t0001g0377a0008c0009t0001g0378 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.600-825T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203403 | ||||||
| chr4:4203452
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.600-874G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203452 | ||||||
| chr4:4203524
|
G | C | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.600-946C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203524 | ||||||
| chr4:4203533
|
T | C | 1 | a0002c0003t0001g0189 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.600-955A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203533 | ||||||
| chr4:4203534
|
A | G | 1 | a0008c0009t0001g0364 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.600-956T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203534 | ||||||
| chr4:4203626
|
C | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(177): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.600-1048G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203626 | ||||||
| chr4:4203707
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.600-1129C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203707 | ||||||
| chr4:4203722
|
C | T | 1 | a0001c0001t0001g0203 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.600-1144G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203722 | ||||||
| chr4:4203838
|
C | A | 8 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0069others(5): Show | 9 | HG02055.hp2 HG02145.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.600-1260G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4203838 | ||||||
| chr4:4204060
|
C | T | 1 | a0008c0009t0001g0367 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.600-1482G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204060 | ||||||
| chr4:4204061
|
G | A | 1 | a0001c0001t0001g0338 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.600-1483C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204061 | ||||||
| chr4:4204079
|
G | A | 2 | a0008c0009t0001g0364a0008c0009t0001g0365 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.600-1501C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204079 | ||||||
| chr4:4204218
|
G | C | 1 | a0001c0001t0001g0242 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.600-1640C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204218 | ||||||
| chr4:4204238
|
G | A | 4 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137others(1): Show | 4 | HG02109.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.600-1660C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204238 | ||||||
| chr4:4204277
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.600-1699A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204277 | ||||||
| chr4:4204341
|
A | G | 23 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(20): Show | 23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.599+1731T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204341 | ||||||
| chr4:4204533
|
G | A | 1 | a0003c0005t0001g0241 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.599+1539C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204533 | ||||||
| chr4:4204559
|
T | C | 3 | a0001c0001t0001g0162a0001c0001t0001g0175a0001c0001t0001g0176 | 3 | HG02056.hp2 NA18966.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.599+1513A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204559 | ||||||
| chr4:4204599
|
G | A | 6 | a0001c0001t0001g0193a0006c0008t0001g0123a0006c0008t0001g0127others(3): Show | 6 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.599+1473C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204599 | ||||||
| chr4:4204712
|
C | CTG | 17 | a0001c0001t0001g0042a0001c0001t0001g0050a0002c0002t0001g0105others(14): Show | 21 | HG00544.hp1 HG00609.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.599+1358_599+1359d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | ||||||
| chr4:4204712
|
CTG | C | 49 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0012others(46): Show | 54 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.599+1358_599+1359d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | ||||||
| chr4:4204712
|
CTGTG | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(25): Show | 36 | HG00621.hp2 HG01993.hp1 HG02015.hp2 others(33): Show |
intron_variant | MODIFIER | c.599+1356_599+1359d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | ||||||
| chr4:4204712
|
CTGTGTG | C | 3 | a0001c0001t0001g0261a0001c0001t0001g0341a0001c0001t0001g0342 | 3 | HG01928.hp1 HG02148.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.599+1354_599+1359d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | ||||||
| chr4:4204712
|
CTGTGTGT others(3): Show |
C | 3 | a0002c0002t0001g0294a0002c0002t0001g0343a0002c0002t0001g0344 | 3 | HG01175.hp1 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.599+1350_599+1359d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | ||||||
| chr4:4204712
|
CTGTGTGT others(9): Show |
C | 9 | a0001c0001t0001g0001a0001c0001t0001g0106a0001c0001t0001g0161others(6): Show | 13 | HG00438.hp1 HG01496.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.599+1344_599+1359d others(18): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | ||||||
| chr4:4204712
|
CTGTGTGT others(11): Show |
C | 200 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(197): Show | 216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.599+1342_599+1359d others(20): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204712 | ||||||
| chr4:4204749
|
T | TGTGC | 2 | a0002c0002t0001g0029a0002c0002t0001g0320 | 3 | NA18954.hp2 NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.599+1322_599+1323i others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204749 | ||||||
| chr4:4204751
|
C | T | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.599+1321G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204751 | ||||||
| chr4:4204895
|
G | A | 1 | a0008c0009t0001g0364 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.599+1177C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4204895 | ||||||
| chr4:4205134
|
T | G | 3 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137 | 3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.599+938A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205134 | ||||||
| chr4:4205137
|
C | T | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0337 | 3 | NA18971.hp2 NA18985.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.599+935G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205137 | ||||||
| chr4:4205226
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(146): Show | 163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.599+846C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205226 | ||||||
| chr4:4205309
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.599+763G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205309 | ||||||
| chr4:4205370
|
C | T | 57 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(54): Show | 65 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.599+702G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205370 | ||||||
| chr4:4205393
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 6 | HG02071.hp2 HG02602.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.599+679C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205393 | ||||||
| chr4:4205395
|
T | C | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.599+677A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205395 | ||||||
| chr4:4205416
|
G | C | 1 | a0009c0012t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.599+656C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205416 | ||||||
| chr4:4205436
|
T | C | 9 | a0001c0001t0001g0142a0001c0001t0001g0147a0001c0001t0001g0148others(6): Show | 9 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.599+636A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205436 | ||||||
| chr4:4205488
|
C | G | 23 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(20): Show | 23 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.599+584G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205488 | ||||||
| chr4:4205592
|
G | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(201): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.599+480C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205592 | ||||||
| chr4:4205639
|
T | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(299): Show | 340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.599+433A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205639 | ||||||
| chr4:4205660
|
G | A | 3 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137 | 3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.599+412C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205660 | ||||||
| chr4:4205710
|
G | C | 1 | a0001c0001t0001g0162 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.599+362C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205710 | ||||||
| chr4:4205766
|
A | G | 2 | a0002c0003t0001g0025a0002c0003t0001g0257 | 3 | HG00673.hp1 HG02040.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.599+306T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205766 | ||||||
| chr4:4205800
|
G | A | 1 | a0002c0003t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.599+272C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205800 | ||||||
| chr4:4205888
|
C | G | 1 | a0008c0009t0001g0363 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.599+184G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205888 | ||||||
| chr4:4205963
|
G | A | 15 | a0001c0001t0001g0020a0001c0001t0001g0233a0003c0005t0001g0023others(12): Show | 17 | HG00544.hp2 HG00738.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.599+109C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 3/5 | chr4 | 4205963 | ||||||
| chr4:4206793
|
T | C | 15 | a0004c0006t0001g0005a0004c0006t0001g0037a0004c0006t0001g0058others(12): Show | 18 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.541-663A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4206793 | ||||||
| chr4:4206851
|
G | A | 7 | a0002c0003t0001g0109a0002c0028t0001g0384a0008c0009t0001g0367others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.541-721C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4206851 | ||||||
| chr4:4206897
|
C | T | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.541-767G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4206897 | ||||||
| chr4:4207015
|
G | A | 1 | a0001c0001t0001g0111 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.541-885C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207015 | ||||||
| chr4:4207074
|
G | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(292): Show | 328 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.541-944C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207074 | ||||||
| chr4:4207134
|
T | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(182): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.541-1004A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207134 | ||||||
| chr4:4207204
|
GCAGT | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.541-1078_541-1075d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207204 | ||||||
| chr4:4207386
|
C | A | 206 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.541-1256G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207386 | ||||||
| chr4:4207573
|
G | T | 1 | a0001c0001t0001g0249 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.541-1443C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207573 | ||||||
| chr4:4207595
|
GTA | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(83): Show | 97 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.541-1467_541-1466d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207595 | ||||||
| chr4:4207595
|
GTATA | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(210): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.541-1469_541-1466d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207595 | ||||||
| chr4:4207630
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(209): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.541-1500C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207630 | ||||||
| chr4:4207687
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.541-1557C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207687 | ||||||
| chr4:4207810
|
A | G | 1 | a0002c0003t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.541-1680T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207810 | ||||||
| chr4:4207823
|
G | C | 1 | a0002c0002t0001g0121 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.541-1693C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207823 | ||||||
| chr4:4207853
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.541-1723A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207853 | ||||||
| chr4:4207864
|
G | C | 2 | a0001c0001t0001g0193a0008c0009t0001g0380 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.541-1734C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207864 | ||||||
| chr4:4207888
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.541-1758C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4207888 | ||||||
| chr4:4208069
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.541-1939C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208069 | ||||||
| chr4:4208108
|
C | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.541-1978G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208108 | ||||||
| chr4:4208340
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0154a0001c0001t0001g0156 | 3 | HG01106.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.541-2210G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208340 | ||||||
| chr4:4208373
|
T | A | 1 | a0011c0014t0001g0366 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.541-2243A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208373 | ||||||
| chr4:4208532
|
C | T | 15 | a0004c0006t0001g0005a0004c0006t0001g0037a0004c0006t0001g0058others(12): Show | 18 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.541-2402G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208532 | ||||||
| chr4:4208733
|
G | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(168): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.541-2603C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208733 | ||||||
| chr4:4208736
|
C | T | 1 | a0002c0002t0001g0301 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.541-2606G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208736 | ||||||
| chr4:4208737
|
G | A | 1 | a0012c0015t0001g0381 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.541-2607C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208737 | ||||||
| chr4:4208738
|
C | T | 1 | a0013c0024t0001g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.541-2608G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208738 | ||||||
| chr4:4208762
|
G | A | 22 | a0001c0004t0001g0039a0001c0004t0001g0040a0001c0004t0001g0048others(19): Show | 22 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.541-2632C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208762 | ||||||
| chr4:4208780
|
TA | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(168): Show | 190 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.541-2651delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208780 | ||||||
| chr4:4208780
|
TAAA | T | 25 | a0001c0001t0001g0283a0001c0004t0001g0039a0001c0004t0001g0040others(22): Show | 25 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.541-2653_541-2651d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208780 | ||||||
| chr4:4208915
|
G | A | 1 | a0002c0002t0001g0319 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.541-2785C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4208915 | ||||||
| chr4:4209051
|
T | C | 1 | a0017c0027t0001g0383 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.541-2921A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209051 | ||||||
| chr4:4209170
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG00639.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.541-3040C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209170 | ||||||
| chr4:4209331
|
C | CAT | 3 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137 | 3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.541-3203_541-3202d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209331 | ||||||
| chr4:4209398
|
G | C | 2 | a0008c0009t0001g0377a0008c0009t0001g0378 | 2 | HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.541-3268C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209398 | ||||||
| chr4:4209408
|
G | T | 15 | a0002c0002t0001g0029a0002c0002t0001g0031a0002c0002t0001g0054others(12): Show | 17 | HG00597.hp2 HG01346.hp1 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.541-3278C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209408 | ||||||
| chr4:4209615
|
C | G | 3 | a0002c0002t0001g0294a0002c0002t0001g0343a0002c0002t0001g0344 | 3 | HG01175.hp1 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.540+3253G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209615 | ||||||
| chr4:4209722
|
G | A | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+3146C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209722 | ||||||
| chr4:4209730
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.540+3138C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209730 | ||||||
| chr4:4209768
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(187): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.540+3100A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209768 | ||||||
| chr4:4209782
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.540+3086A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209782 | ||||||
| chr4:4209838
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.540+3030C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209838 | ||||||
| chr4:4209963
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(187): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.540+2905A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4209963 | ||||||
| chr4:4210069
|
G | A | 2 | a0001c0001t0001g0193a0008c0009t0001g0380 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.540+2799C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210069 | ||||||
| chr4:4210110
|
C | T | 3 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137 | 3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.540+2758G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210110 | ||||||
| chr4:4210114
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.540+2754T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210114 | ||||||
| chr4:4210162
|
C | T | 1 | a0005c0007t0001g0356 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.540+2706G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210162 | ||||||
| chr4:4210169
|
C | T | 2 | a0009c0012t0001g0125a0009c0012t0001g0137 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.540+2699G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210169 | ||||||
| chr4:4210199
|
A | AAATG | 7 | a0002c0003t0001g0109a0002c0028t0001g0384a0008c0009t0001g0367others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+2665_540+2668d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210199 | ||||||
| chr4:4210354
|
C | A | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+2514G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210354 | ||||||
| chr4:4210396
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.540+2472G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210396 | ||||||
| chr4:4210397
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.540+2471C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210397 | ||||||
| chr4:4210422
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.540+2446T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210422 | ||||||
| chr4:4210483
|
G | A | 15 | a0001c0001t0001g0019a0001c0001t0001g0184a0001c0001t0001g0185others(12): Show | 16 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.540+2385C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210483 | ||||||
| chr4:4210558
|
C | T | 3 | a0006c0008t0001g0123a0006c0008t0001g0127a0006c0008t0001g0129 | 3 | HG01891.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.540+2310G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210558 | ||||||
| chr4:4210581
|
A | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2287T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210581 | ||||||
| chr4:4210586
|
T | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2282A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210586 | ||||||
| chr4:4210588
|
T | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2280A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210588 | ||||||
| chr4:4210589
|
G | C | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2279C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210589 | ||||||
| chr4:4210590
|
G | C | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2278C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210590 | ||||||
| chr4:4210591
|
G | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2277C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210591 | ||||||
| chr4:4210592
|
A | C | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2276T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210592 | ||||||
| chr4:4210593
|
G | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2275C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210593 | ||||||
| chr4:4210594
|
G | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2274C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210594 | ||||||
| chr4:4210596
|
C | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2272G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210596 | ||||||
| chr4:4210597
|
G | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2271C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210597 | ||||||
| chr4:4210603
|
G | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2265C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210603 | ||||||
| chr4:4210604
|
G | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2264C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210604 | ||||||
| chr4:4210606
|
G | C | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2262C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210606 | ||||||
| chr4:4210607
|
G | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2261C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210607 | ||||||
| chr4:4210608
|
A | C | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2260T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210608 | ||||||
| chr4:4210609
|
T | C | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2259A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210609 | ||||||
| chr4:4210610
|
T | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2258A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210610 | ||||||
| chr4:4210611
|
G | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2257C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210611 | ||||||
| chr4:4210613
|
C | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2255G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210613 | ||||||
| chr4:4210615
|
G | C | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2253C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210615 | ||||||
| chr4:4210616
|
A | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2252T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210616 | ||||||
| chr4:4210617
|
G | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2251C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210617 | ||||||
| chr4:4210623
|
G | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2245C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210623 | ||||||
| chr4:4210625
|
G | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2243C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210625 | ||||||
| chr4:4210626
|
T | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2242A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210626 | ||||||
| chr4:4210627
|
T | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2241A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210627 | ||||||
| chr4:4210629
|
G | T | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2239C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210629 | ||||||
| chr4:4210631
|
G | A | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2237C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210631 | ||||||
| chr4:4210633
|
C | G | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+2235G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210633 | ||||||
| chr4:4210635
|
A | C | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2233T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210635 | ||||||
| chr4:4210636
|
G | C | 1 | a0002c0002t0001g0314 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.540+2232C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210636 | ||||||
| chr4:4210787
|
C | T | 7 | a0002c0003t0001g0109a0002c0028t0001g0384a0008c0009t0001g0367others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+2081G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210787 | ||||||
| chr4:4210869
|
G | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0359 | 3 | HG02451.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.540+1999C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210869 | ||||||
| chr4:4210911
|
C | T | 1 | a0003c0005t0001g0232 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.540+1957G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210911 | ||||||
| chr4:4210997
|
C | T | 3 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137 | 3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.540+1871G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4210997 | ||||||
| chr4:4211066
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(189): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.540+1802A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211066 | ||||||
| chr4:4211140
|
T | C | 6 | a0002c0028t0001g0384a0008c0009t0001g0367a0008c0009t0001g0377others(3): Show | 6 | HG01891.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+1728A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211140 | ||||||
| chr4:4211204
|
C | A | 13 | a0001c0001t0001g0142a0001c0001t0001g0147a0001c0001t0001g0148others(10): Show | 13 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+1664G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211204 | ||||||
| chr4:4211207
|
G | A | 19 | a0001c0004t0001g0048a0001c0004t0001g0059a0001c0004t0001g0060others(16): Show | 19 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.540+1661C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211207 | ||||||
| chr4:4211292
|
C | G | 7 | a0002c0003t0001g0109a0002c0028t0001g0384a0008c0009t0001g0367others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+1576G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211292 | ||||||
| chr4:4211348
|
C | T | 5 | a0003c0005t0001g0112a0003c0005t0001g0138a0003c0005t0001g0166others(2): Show | 5 | HG00544.hp2 NA18952.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+1520G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211348 | ||||||
| chr4:4211361
|
G | A | 20 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(17): Show | 24 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.540+1507C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211361 | ||||||
| chr4:4211385
|
C | T | 2 | a0001c0004t0001g0190a0008c0026t0001g0376 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.540+1483G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211385 | ||||||
| chr4:4211438
|
ACTT | A | 19 | a0001c0004t0001g0048a0001c0004t0001g0059a0001c0004t0001g0060others(16): Show | 19 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.540+1427_540+1429d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211438 | ||||||
| chr4:4211477
|
T | C | 1 | a0009c0018t0001g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.540+1391A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211477 | ||||||
| chr4:4211496
|
T | C | 13 | a0001c0001t0001g0142a0001c0001t0001g0147a0001c0001t0001g0148others(10): Show | 13 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+1372A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211496 | ||||||
| chr4:4211583
|
C | T | 15 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 18 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.540+1285G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211583 | ||||||
| chr4:4211612
|
A | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.540+1256T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211612 | ||||||
| chr4:4211647
|
C | T | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+1221G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211647 | ||||||
| chr4:4211666
|
G | C | 15 | a0001c0001t0001g0019a0001c0001t0001g0184a0001c0001t0001g0185others(12): Show | 16 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.540+1202C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211666 | ||||||
| chr4:4211767
|
T | G | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+1101A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211767 | ||||||
| chr4:4211881
|
A | T | 1 | a0002c0002t0001g0312 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.540+987T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211881 | ||||||
| chr4:4211938
|
A | T | 2 | a0002c0002t0001g0296a0002c0002t0001g0297 | 2 | HG02056.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.540+930T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4211938 | ||||||
| chr4:4212005
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.540+863T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212005 | ||||||
| chr4:4212118
|
T | C | 3 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137 | 3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.540+750A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212118 | ||||||
| chr4:4212138
|
T | C | 3 | a0002c0002t0001g0294a0002c0002t0001g0343a0002c0002t0001g0344 | 3 | HG01175.hp1 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.540+730A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212138 | ||||||
| chr4:4212226
|
T | C | 3 | a0008c0009t0001g0367a0011c0014t0001g0366a0011c0014t0001g0368 | 3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.540+642A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212226 | ||||||
| chr4:4212307
|
G | T | 7 | a0002c0003t0001g0109a0002c0028t0001g0384a0008c0009t0001g0367others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.540+561C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212307 | ||||||
| chr4:4212381
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0154a0001c0001t0001g0156 | 3 | HG01106.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.540+487G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212381 | ||||||
| chr4:4212448
|
A | G | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+420T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212448 | ||||||
| chr4:4212557
|
T | C | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.540+311A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212557 | ||||||
| chr4:4212822
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0220 | 3 | HG02129.hp2 NA18968.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.540+46T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 2/5 | chr4 | 4212822 | ||||||
| chr4:4213043
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.404-39A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213043 | ||||||
| chr4:4213208
|
G | A | 3 | a0001c0001t0001g0015a0001c0004t0001g0190a0008c0026t0001g0376 | 4 | HG02280.hp2 HG02622.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-204C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213208 | ||||||
| chr4:4213329
|
G | T | 1 | a0001c0001t0001g0082 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.404-325C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213329 | ||||||
| chr4:4213445
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(185): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.404-441C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213445 | ||||||
| chr4:4213450
|
G | A | 1 | a0004c0006t0001g0058 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.404-446C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213450 | ||||||
| chr4:4213453
|
A | G | 2 | a0001c0004t0001g0190a0008c0026t0001g0376 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-449T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213453 | ||||||
| chr4:4213460
|
A | G | 46 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0152others(43): Show | 47 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.404-456T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213460 | ||||||
| chr4:4213580
|
T | C | 12 | a0002c0003t0001g0096a0002c0003t0001g0097a0002c0013t0001g0100others(9): Show | 12 | HG01167.hp1 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.404-576A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213580 | ||||||
| chr4:4213597
|
C | T | 2 | a0009c0012t0001g0125a0009c0012t0001g0137 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.404-593G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213597 | ||||||
| chr4:4213601
|
T | A | 1 | a0002c0013t0001g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.404-597A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213601 | ||||||
| chr4:4213647
|
C | T | 1 | a0002c0002t0001g0317 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.404-643G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213647 | ||||||
| chr4:4213730
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.404-726G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213730 | ||||||
| chr4:4213731
|
G | A | 1 | a0002c0002t0001g0302 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.404-727C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213731 | ||||||
| chr4:4213816
|
A | T | 2 | a0009c0012t0001g0160a0018c0016t0001g0033 | 2 | HG03927.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.404-812T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213816 | ||||||
| chr4:4213868
|
T | C | 34 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(31): Show | 39 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.404-864A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213868 | ||||||
| chr4:4213963
|
G | T | 1 | a0001c0004t0001g0231 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.404-959C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4213963 | ||||||
| chr4:4214006
|
CT | C | 6 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0079others(3): Show | 6 | HG00438.hp2 HG02074.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.404-1003delA | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214006 | ||||||
| chr4:4214041
|
G | A | 1 | a0002c0003t0001g0186 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.404-1037C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214041 | ||||||
| chr4:4214329
|
T | C | 2 | a0001c0004t0001g0190a0008c0026t0001g0376 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-1325A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214329 | ||||||
| chr4:4214417
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.404-1413G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214417 | ||||||
| chr4:4214461
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0259 | 4 | NA18940.hp2 NA18945.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1457T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214461 | ||||||
| chr4:4214490
|
A | C | 1 | a0001c0001t0001g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.404-1486T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214490 | ||||||
| chr4:4214511
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.404-1507A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214511 | ||||||
| chr4:4214531
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.404-1527A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214531 | ||||||
| chr4:4214769
|
A | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0184others(13): Show | 17 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-1765T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214769 | ||||||
| chr4:4214800
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.404-1796T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214800 | ||||||
| chr4:4214834
|
G | C | 20 | a0002c0002t0001g0029a0002c0002t0001g0031a0002c0002t0001g0054others(17): Show | 27 | HG00609.hp1 HG00673.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.404-1830C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214834 | ||||||
| chr4:4214851
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.404-1847G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214851 | ||||||
| chr4:4214871
|
G | C | 1 | a0002c0013t0001g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.404-1867C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214871 | ||||||
| chr4:4214953
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.404-1949C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214953 | ||||||
| chr4:4214966
|
CA | C | 4 | a0002c0003t0001g0109a0002c0028t0001g0384a0008c0009t0001g0377others(1): Show | 4 | HG02257.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-1963delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214966 | ||||||
| chr4:4214969
|
A | G | 19 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(16): Show | 23 | HG00735.hp2 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.404-1965T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214969 | ||||||
| chr4:4214972
|
T | TAAAAATA others(344): Show |
1 | a0002c0002t0001g0345 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.404-1969_404-1968i others(353): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214972 | ||||||
| chr4:4214991
|
T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(80): Show | 93 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.404-1987A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4214991 | ||||||
| chr4:4215068
|
G | A | 1 | a0019c0017t0001g0034 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.404-2064C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215068 | ||||||
| chr4:4215224
|
G | C | 24 | a0001c0001t0001g0193a0001c0004t0001g0048a0001c0004t0001g0059others(21): Show | 24 | HG00140.hp1 HG00642.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-2220C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215224 | ||||||
| chr4:4215235
|
C | A | 2 | a0002c0002t0001g0324a0002c0002t0001g0325 | 2 | HG01952.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.404-2231G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215235 | ||||||
| chr4:4215263
|
C | A | 7 | a0002c0003t0001g0109a0002c0028t0001g0384a0008c0009t0001g0363others(4): Show | 7 | HG02109.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-2259G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215263 | ||||||
| chr4:4215385
|
G | A | 3 | a0002c0002t0001g0090a0002c0002t0001g0221a0002c0002t0001g0222 | 3 | NA18966.hp2 NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.404-2381C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215385 | ||||||
| chr4:4215427
|
T | C | 61 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(58): Show | 66 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.404-2423A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215427 | ||||||
| chr4:4215433
|
G | A | 13 | a0001c0001t0001g0142a0001c0001t0001g0147a0001c0001t0001g0148others(10): Show | 13 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.404-2429C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215433 | ||||||
| chr4:4215459
|
C | T | 1 | a0002c0002t0001g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.404-2455G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215459 | ||||||
| chr4:4215468
|
C | G | 2 | a0001c0004t0001g0190a0008c0026t0001g0376 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-2464G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215468 | ||||||
| chr4:4215493
|
C | A | 1 | a0002c0002t0001g0302 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.404-2489G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215493 | ||||||
| chr4:4215521
|
T | C | 62 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(59): Show | 67 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.404-2517A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215521 | ||||||
| chr4:4215550
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(124): Show | 140 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.404-2546G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215550 | ||||||
| chr4:4215589
|
A | G | 62 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(59): Show | 67 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.404-2585T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215589 | ||||||
| chr4:4215686
|
T | TA | 62 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(59): Show | 67 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.404-2683dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215686 | ||||||
| chr4:4215724
|
A | G | 62 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0017others(59): Show | 67 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.404-2720T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215724 | ||||||
| chr4:4215987
|
T | G | 1 | a0008c0009t0001g0367 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.404-2983A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4215987 | ||||||
| chr4:4216054
|
T | C | 123 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(120): Show | 140 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.404-3050A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216054 | ||||||
| chr4:4216078
|
C | A | 80 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(77): Show | 96 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.404-3074G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216078 | ||||||
| chr4:4216084
|
T | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0184others(13): Show | 17 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-3080A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216084 | ||||||
| chr4:4216091
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0184others(13): Show | 17 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-3087C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216091 | ||||||
| chr4:4216193
|
C | A | 33 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 38 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.404-3189G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216193 | ||||||
| chr4:4216257
|
T | G | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.404-3253A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216257 | ||||||
| chr4:4216309
|
G | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0079others(3): Show | 6 | HG00438.hp2 HG02074.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.404-3305C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216309 | ||||||
| chr4:4216315
|
T | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0113others(8): Show | 12 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.404-3311A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216315 | ||||||
| chr4:4216357
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0184others(13): Show | 17 | HG01891.hp1 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.404-3353C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216357 | ||||||
| chr4:4216382
|
T | G | 1 | a0002c0002t0001g0321 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.404-3378A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216382 | ||||||
| chr4:4216395
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.404-3391A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216395 | ||||||
| chr4:4216423
|
C | T | 2 | a0002c0003t0001g0126a0007c0010t0001g0379 | 2 | HG01109.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.404-3419G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216423 | ||||||
| chr4:4216443
|
C | T | 1 | a0013c0024t0001g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.404-3439G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216443 | ||||||
| chr4:4216518
|
C | T | 3 | a0001c0001t0001g0283a0009c0012t0001g0160a0018c0016t0001g0033 | 3 | HG03927.hp1 HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.404-3514G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216518 | ||||||
| chr4:4216525
|
C | G | 378 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(375): Show | 420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.404-3521G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216525 | ||||||
| chr4:4216571
|
C | T | 2 | a0001c0001t0001g0233a0003c0005t0001g0232 | 2 | HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.404-3567G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216571 | ||||||
| chr4:4216603
|
C | G | 3 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137 | 3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.404-3599G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216603 | ||||||
| chr4:4216775
|
A | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(111): Show | 129 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.404-3771T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216775 | ||||||
| chr4:4216780
|
A | T | 1 | a0004c0006t0001g0274 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.404-3776T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216780 | ||||||
| chr4:4216804
|
G | A | 2 | a0001c0001t0001g0193a0008c0009t0001g0380 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404-3800C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216804 | ||||||
| chr4:4216942
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.404-3938G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216942 | ||||||
| chr4:4216974
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(241): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.404-3970T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4216974 | ||||||
| chr4:4217151
|
G | A | 1 | a0001c0004t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.404-4147C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217151 | ||||||
| chr4:4217221
|
T | C | 2 | a0001c0004t0001g0190a0008c0026t0001g0376 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-4217A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217221 | ||||||
| chr4:4217225
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.404-4221A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217225 | ||||||
| chr4:4217361
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.404-4357G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217361 | ||||||
| chr4:4217495
|
T | C | 1 | a0007c0010t0001g0374 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.404-4491A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217495 | ||||||
| chr4:4217556
|
T | C | 2 | a0001c0004t0001g0190a0008c0026t0001g0376 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-4552A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217556 | ||||||
| chr4:4217651
|
T | C | 2 | a0001c0001t0001g0193a0008c0009t0001g0380 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.404-4647A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217651 | ||||||
| chr4:4217712
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.404-4708C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217712 | ||||||
| chr4:4217746
|
G | A | 19 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0184others(16): Show | 20 | HG01255.hp1 HG01891.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.404-4742C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217746 | ||||||
| chr4:4217782
|
T | A | 1 | a0001c0001t0001g0354 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.404-4778A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217782 | ||||||
| chr4:4217819
|
A | G | 5 | a0001c0001t0001g0193a0008c0009t0001g0363a0008c0009t0001g0380others(2): Show | 5 | HG02109.hp2 HG02717.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-4815T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217819 | ||||||
| chr4:4217852
|
G | C | 1 | a0003c0005t0001g0271 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.404-4848C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217852 | ||||||
| chr4:4217863
|
A | G | 19 | a0001c0001t0001g0193a0001c0001t0001g0283a0001c0004t0001g0048others(16): Show | 19 | HG00738.hp1 HG01123.hp1 HG02004.hp2 others(16): Show |
intron_variant | MODIFIER | c.404-4859T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217863 | ||||||
| chr4:4217878
|
T | C | 4 | a0002c0003t0001g0109a0002c0028t0001g0384a0008c0009t0001g0377others(1): Show | 4 | HG02257.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-4874A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217878 | ||||||
| chr4:4217883
|
A | G | 4 | a0002c0003t0001g0109a0002c0028t0001g0384a0008c0009t0001g0377others(1): Show | 4 | HG02257.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.404-4879T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4217883 | ||||||
| chr4:4218003
|
T | G | 1 | a0002c0002t0001g0315 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.404-4999A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218003 | ||||||
| chr4:4218076
|
T | C | 3 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137 | 3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.404-5072A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218076 | ||||||
| chr4:4218088
|
T | C | 22 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0184others(19): Show | 23 | HG01255.hp1 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.404-5084A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218088 | ||||||
| chr4:4218305
|
T | C | 3 | a0008c0009t0001g0363a0009c0012t0001g0125a0009c0012t0001g0137 | 3 | HG02109.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.404-5301A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218305 | ||||||
| chr4:4218349
|
G | A | 2 | a0008c0009t0001g0364a0008c0009t0001g0365 | 2 | HG02559.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.404-5345C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218349 | ||||||
| chr4:4218378
|
C | T | 3 | a0008c0009t0001g0367a0011c0014t0001g0366a0011c0014t0001g0368 | 3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-5374G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218378 | ||||||
| chr4:4218379
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA18747.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.404-5375C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218379 | ||||||
| chr4:4218391
|
C | CA | 219 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(216): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.404-5388dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218391 | ||||||
| chr4:4218391
|
C | CAA | 23 | a0001c0001t0001g0019a0001c0001t0001g0117a0001c0001t0001g0130others(20): Show | 24 | HG01192.hp2 HG01255.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.404-5389_404-5388d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218391 | ||||||
| chr4:4218456
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.404-5452G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218456 | ||||||
| chr4:4218533
|
C | A | 3 | a0008c0009t0001g0367a0011c0014t0001g0366a0011c0014t0001g0368 | 3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-5529G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218533 | ||||||
| chr4:4218549
|
G | A | 1 | a0001c0001t0001g0014 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.404-5545C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218549 | ||||||
| chr4:4218599
|
G | A | 3 | a0008c0009t0001g0367a0011c0014t0001g0366a0011c0014t0001g0368 | 3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-5595C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218599 | ||||||
| chr4:4218648
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(137): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.404-5644G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218648 | ||||||
| chr4:4218717
|
C | G | 7 | a0002c0003t0001g0186a0002c0003t0001g0227a0006c0008t0001g0123others(4): Show | 7 | HG01255.hp1 HG01891.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.404-5713G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218717 | ||||||
| chr4:4218735
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.404-5731G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218735 | ||||||
| chr4:4218747
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.404-5743C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218747 | ||||||
| chr4:4218748
|
T | C | 1 | a0002c0002t0001g0311 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.404-5744A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218748 | ||||||
| chr4:4218778
|
C | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(157): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.404-5774G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218778 | ||||||
| chr4:4218798
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.404-5794C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218798 | ||||||
| chr4:4218877
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.404-5873G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218877 | ||||||
| chr4:4218878
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.404-5874T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218878 | ||||||
| chr4:4218879
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.404-5875T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218879 | ||||||
| chr4:4218885
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.404-5881A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218885 | ||||||
| chr4:4218890
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.404-5886G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218890 | ||||||
| chr4:4218891
|
T | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.404-5887A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218891 | ||||||
| chr4:4218925
|
T | C | 1 | a0008c0009t0001g0363 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.404-5921A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218925 | ||||||
| chr4:4218933
|
A | G | 2 | a0001c0004t0001g0190a0008c0026t0001g0376 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.404-5929T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218933 | ||||||
| chr4:4218975
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0001g0187 | 3 | HG01884.hp2 HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.404-5971C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218975 | ||||||
| chr4:4218998
|
G | C | 1 | a0001c0001t0001g0264 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.404-5994C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4218998 | ||||||
| chr4:4219118
|
CAAAA | C | 5 | a0001c0001t0001g0193a0008c0009t0001g0367a0008c0009t0001g0380others(2): Show | 5 | HG01891.hp2 HG03471.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.404-6118_404-6115d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219118 | ||||||
| chr4:4219158
|
T | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0130a0001c0001t0001g0191others(3): Show | 7 | HG02109.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.404-6154A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219158 | ||||||
| chr4:4219199
|
G | C | 1 | a0017c0027t0001g0383 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.404-6195C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219199 | ||||||
| chr4:4219243
|
T | C | 3 | a0008c0009t0001g0367a0011c0014t0001g0366a0011c0014t0001g0368 | 3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-6239A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219243 | ||||||
| chr4:4219390
|
C | T | 1 | a0001c0001t0001g0334 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.404-6386G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219390 | ||||||
| chr4:4219395
|
T | A | 1 | a0001c0001t0001g0242 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.404-6391A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219395 | ||||||
| chr4:4219428
|
G | A | 2 | a0001c0001t0001g0074a0009c0018t0001g0035 | 2 | HG02083.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.404-6424C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219428 | ||||||
| chr4:4219429
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.404-6425G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219429 | ||||||
| chr4:4219472
|
C | T | 1 | a0002c0002t0001g0131 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.404-6468G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219472 | ||||||
| chr4:4219498
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.404-6494C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219498 | ||||||
| chr4:4219512
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(262): Show | 298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.404-6508G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219512 | ||||||
| chr4:4219518
|
G | A | 1 | a0009c0012t0001g0160 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.404-6514C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219518 | ||||||
| chr4:4219571
|
G | A | 1 | a0002c0002t0001g0105 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.404-6567C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219571 | ||||||
| chr4:4219574
|
T | C | 3 | a0008c0009t0001g0367a0011c0014t0001g0366a0011c0014t0001g0368 | 3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.404-6570A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219574 | ||||||
| chr4:4219592
|
T | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0144 | 2 | HG01070.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.404-6588A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219592 | ||||||
| chr4:4219669
|
C | G | 1 | a0002c0013t0001g0226 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.404-6665G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219669 | ||||||
| chr4:4219684
|
G | A | 1 | a0002c0002t0001g0346 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.404-6680C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219684 | ||||||
| chr4:4219692
|
G | A | 1 | a0013c0024t0001g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.404-6688C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219692 | ||||||
| chr4:4219696
|
C | CAA | 137 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(134): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.404-6694_404-6693d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219696 | ||||||
| chr4:4219798
|
A | C | 2 | a0002c0002t0001g0346a0003c0005t0001g0238 | 2 | HG01081.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.403+6664T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219798 | ||||||
| chr4:4219809
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0290a0001c0001t0001g0336 | 7 | HG00438.hp1 NA18946.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+6653C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219809 | ||||||
| chr4:4219809
|
G | GTGTATAT others(39): Show |
1 | a0001c0001t0001g0072 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.403+6607_403+6652d others(48): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219809 | ||||||
| chr4:4219836
|
C | CAT | 131 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.403+6624_403+6625d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219836 | ||||||
| chr4:4219837
|
A | ATATATAT others(33): Show |
1 | a0002c0003t0001g0225 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.403+6585_403+6624d others(42): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219837 | ||||||
| chr4:4219856
|
T | C | 1 | a0002c0002t0001g0346 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.403+6606A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219856 | ||||||
| chr4:4219884
|
T | C | 15 | a0004c0006t0001g0005a0004c0006t0001g0037a0004c0006t0001g0058others(12): Show | 17 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.403+6578A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219884 | ||||||
| chr4:4219895
|
G | GTATACAC others(35): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0152 | 6 | NA18939.hp1 NA18970.hp1 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+6566_403+6567i others(44): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219895 | ||||||
| chr4:4219913
|
G | GTATATAC others(25): Show |
2 | a0001c0004t0001g0190a0008c0026t0001g0376 | 2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.403+6517_403+6548d others(34): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219913 | ||||||
| chr4:4219915
|
A | G | 133 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.403+6547T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219915 | ||||||
| chr4:4219935
|
A | G | 1 | a0001c0004t0001g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.403+6527T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219935 | ||||||
| chr4:4219940
|
T | C | 4 | a0002c0003t0001g0126a0002c0003t0001g0188a0009c0012t0001g0125others(1): Show | 4 | HG01243.hp1 HG02109.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+6522A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219940 | ||||||
| chr4:4219952
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.403+6510G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219952 | ||||||
| chr4:4219967
|
A | G | 1 | a0001c0004t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.403+6495T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219967 | ||||||
| chr4:4219985
|
G | A | 5 | a0001c0001t0001g0334a0002c0002t0001g0335a0008c0009t0001g0367others(2): Show | 5 | HG01891.hp2 NA18522.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+6477C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4219985 | ||||||
| chr4:4220009
|
A | ATGTATAT others(41): Show |
4 | a0001c0004t0001g0250a0002c0002t0001g0300a0002c0002t0001g0316others(1): Show | 4 | HG01123.hp1 HG01361.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+6405_403+6452d others(50): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220009 | ||||||
| chr4:4220010
|
T | G | 1 | a0017c0027t0001g0383 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.403+6452A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220010 | ||||||
| chr4:4220011
|
GTA | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(292): Show | 330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.403+6449_403+6450d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220011 | ||||||
| chr4:4220020
|
T | C | 1 | a0005c0007t0001g0352 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.403+6442A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220020 | ||||||
| chr4:4220024
|
TATACGTA others(19): Show |
T | 2 | a0004c0006t0001g0124a0004c0006t0001g0181 | 2 | HG02965.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.403+6412_403+6437d others(28): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220024 | ||||||
| chr4:4220029
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(294): Show | 332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.403+6433C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220029 | ||||||
| chr4:4220048
|
TAC | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(237): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.403+6412_403+6413d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220048 | ||||||
| chr4:4220050
|
C | T | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0012others(51): Show | 63 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.403+6412G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220050 | ||||||
| chr4:4220067
|
A | ATGTATAT others(3): Show |
1 | a0002c0002t0001g0329 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.403+6394_403+6395i others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220067 | ||||||
| chr4:4220080
|
CAT | C | 169 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(166): Show | 189 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.403+6380_403+6381d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220080 | ||||||
| chr4:4220080
|
CATAT | C | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0019others(58): Show | 68 | HG00438.hp1 HG00597.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.403+6378_403+6381d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220080 | ||||||
| chr4:4220080
|
CATATAT | C | 5 | a0001c0001t0001g0089a0002c0028t0001g0384a0008c0009t0001g0367others(2): Show | 5 | HG01891.hp2 HG02922.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+6376_403+6381d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220080 | ||||||
| chr4:4220084
|
T | TATACATA others(27): Show |
1 | a0002c0002t0001g0329 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.403+6377_403+6378i others(36): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220084 | ||||||
| chr4:4220084
|
T | TATATATA others(27): Show |
1 | a0001c0001t0001g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.403+6377_403+6378i others(36): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220084 | ||||||
| chr4:4220098
|
TA | T | 9 | a0002c0003t0001g0189a0002c0003t0001g0225a0007c0010t0001g0370others(6): Show | 9 | HG02109.hp2 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+6363delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220098 | ||||||
| chr4:4220098
|
TATA | T | 20 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0113others(17): Show | 24 | HG01884.hp2 HG02015.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.403+6361_403+6363d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220098 | ||||||
| chr4:4220098
|
TATATA | T | 21 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0043others(18): Show | 23 | HG00597.hp1 HG00621.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.403+6359_403+6363d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220098 | ||||||
| chr4:4220099
|
A | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0191others(16): Show | 21 | HG01167.hp1 HG01255.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.403+6363T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220099 | ||||||
| chr4:4220100
|
TATA | T | 12 | a0001c0001t0001g0216a0001c0001t0001g0220a0001c0001t0001g0340others(9): Show | 12 | HG00609.hp1 HG02056.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.403+6359_403+6361d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220100 | ||||||
| chr4:4220100
|
TATATA | T | 8 | a0001c0001t0001g0014a0001c0001t0001g0087a0001c0001t0001g0088others(5): Show | 9 | HG00438.hp2 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+6357_403+6361d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220100 | ||||||
| chr4:4220101
|
A | T | 59 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(56): Show | 62 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.403+6361T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220101 | ||||||
| chr4:4220102
|
TATA | T | 16 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(13): Show | 18 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.403+6357_403+6359d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220102 | ||||||
| chr4:4220103
|
A | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 130 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.403+6359T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220103 | ||||||
| chr4:4220103
|
ATAT | A | 7 | a0001c0001t0001g0322a0001c0004t0001g0190a0001c0004t0001g0250others(4): Show | 7 | HG00099.hp1 HG01123.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+6356_403+6358d others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220103 | ||||||
| chr4:4220104
|
TA | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0051a0001c0001t0001g0061others(2): Show | 6 | HG00673.hp2 HG00735.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+6357delT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220104 | ||||||
| chr4:4220105
|
A | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.403+6357T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220105 | ||||||
| chr4:4220105
|
ATT | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0251a0001c0001t0001g0272others(4): Show | 7 | HG01952.hp2 HG02129.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.403+6355_403+6356d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220105 | ||||||
| chr4:4220107
|
T | A | 2 | a0002c0002t0001g0323a0002c0002t0001g0324 | 2 | HG01993.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.403+6355A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220107 | ||||||
| chr4:4220120
|
G | A | 2 | a0002c0002t0001g0093a0002c0002t0001g0164 | 2 | HG01123.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.403+6342C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220120 | ||||||
| chr4:4220141
|
C | T | 1 | a0002c0002t0001g0140 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.403+6321G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220141 | ||||||
| chr4:4220181
|
T | C | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(376): Show | 421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.403+6281A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220181 | ||||||
| chr4:4220188
|
C | T | 3 | a0001c0001t0001g0193a0008c0009t0001g0380a0009c0018t0001g0035 | 3 | HG02809.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.403+6274G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220188 | ||||||
| chr4:4220327
|
T | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(39): Show | 47 | HG00621.hp1 HG01243.hp1 HG02015.hp2 others(44): Show |
intron_variant | MODIFIER | c.403+6135A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220327 | ||||||
| chr4:4220332
|
C | T | 25 | a0001c0001t0001g0015a0001c0001t0001g0113a0001c0001t0001g0114others(22): Show | 26 | HG00733.hp2 HG01167.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.403+6130G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220332 | ||||||
| chr4:4220351
|
G | A | 4 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0359others(1): Show | 4 | HG02451.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+6111C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220351 | ||||||
| chr4:4220394
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0012others(48): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.403+6068T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220394 | ||||||
| chr4:4220400
|
G | A | 3 | a0001c0001t0001g0193a0008c0009t0001g0380a0009c0018t0001g0035 | 3 | HG02809.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.403+6062C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220400 | ||||||
| chr4:4220650
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.403+5812A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220650 | ||||||
| chr4:4220852
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0113a0001c0001t0001g0114others(8): Show | 12 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.403+5610G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220852 | ||||||
| chr4:4220868
|
A | G | 1 | a0013c0024t0001g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403+5594T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220868 | ||||||
| chr4:4220970
|
G | T | 1 | a0004c0006t0001g0299 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.403+5492C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220970 | ||||||
| chr4:4220979
|
T | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(206): Show | 238 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.403+5483A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220979 | ||||||
| chr4:4220992
|
G | T | 1 | a0013c0024t0001g0362 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.403+5470C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4220992 | ||||||
| chr4:4221038
|
T | G | 6 | a0001c0001t0001g0130a0002c0003t0001g0128a0006c0008t0001g0123others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+5424A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221038 | ||||||
| chr4:4221043
|
C | CTATTT | 27 | a0001c0001t0001g0015a0001c0001t0001g0092a0001c0001t0001g0113others(24): Show | 28 | HG01243.hp2 HG01433.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.403+5414_403+5418d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | ||||||
| chr4:4221043
|
C | CTATTTTA others(3): Show |
15 | a0001c0001t0001g0068a0001c0001t0001g0114a0001c0001t0001g0177others(12): Show | 16 | HG01167.hp1 HG01257.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.403+5409_403+5418d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | ||||||
| chr4:4221043
|
C | CTATTTTA others(8): Show |
9 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(6): Show | 9 | HG02735.hp2 HG03491.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.403+5404_403+5418d others(17): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | ||||||
| chr4:4221043
|
C | CTATTTTA others(13): Show |
3 | a0001c0001t0001g0061a0001c0004t0001g0170a0002c0013t0001g0122 | 3 | HG03195.hp2 HG04228.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.403+5399_403+5418d others(22): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | ||||||
| chr4:4221043
|
C | CTATTTTA others(18): Show |
1 | a0011c0014t0001g0366 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.403+5394_403+5418d others(27): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | ||||||
| chr4:4221043
|
CTATTT | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.403+5414_403+5418d others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | ||||||
| chr4:4221043
|
CTATTTTA others(3): Show |
C | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 109 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.403+5409_403+5418d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | ||||||
| chr4:4221043
|
CTATTTTA others(8): Show |
C | 19 | a0001c0001t0001g0130a0001c0001t0001g0184a0001c0001t0001g0185others(16): Show | 19 | HG01175.hp1 HG01891.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.403+5404_403+5418d others(17): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | ||||||
| chr4:4221043
|
CTATTTTA others(13): Show |
C | 9 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(6): Show | 10 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.403+5399_403+5418d others(22): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221043 | ||||||
| chr4:4221295
|
C | T | 3 | a0008c0009t0001g0367a0011c0014t0001g0366a0011c0014t0001g0368 | 3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+5167G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221295 | ||||||
| chr4:4221349
|
A | G | 1 | a0002c0002t0001g0300 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.403+5113T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221349 | ||||||
| chr4:4221350
|
G | C | 1 | a0001c0001t0001g0234 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.403+5112C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221350 | ||||||
| chr4:4221355
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.403+5107A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221355 | ||||||
| chr4:4221384
|
C | T | 20 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(17): Show | 20 | HG01891.hp2 HG02257.hp2 HG02698.hp1 others(17): Show |
intron_variant | MODIFIER | c.403+5078G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221384 | ||||||
| chr4:4221467
|
AG | A | 25 | a0001c0001t0001g0015a0001c0001t0001g0113a0001c0001t0001g0114others(22): Show | 26 | HG00733.hp2 HG01167.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.403+4994delC | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221467 | ||||||
| chr4:4221535
|
C | T | 1 | a0004c0006t0001g0299 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.403+4927G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221535 | ||||||
| chr4:4221895
|
T | C | 28 | a0001c0001t0001g0015a0001c0001t0001g0113a0001c0001t0001g0114others(25): Show | 29 | HG00733.hp2 HG01167.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.403+4567A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4221895 | ||||||
| chr4:4222082
|
G | T | 1 | a0008c0009t0001g0363 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.403+4380C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222082 | ||||||
| chr4:4222285
|
G | A | 1 | a0007c0010t0001g0369 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.403+4177C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222285 | ||||||
| chr4:4222388
|
G | A | 1 | a0007c0025t0001g0375 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.403+4074C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222388 | ||||||
| chr4:4222522
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.403+3940G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222522 | ||||||
| chr4:4222550
|
G | A | 2 | a0012c0015t0001g0381a0012c0015t0001g0382 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.403+3912C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222550 | ||||||
| chr4:4222669
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.403+3793G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222669 | ||||||
| chr4:4222744
|
G | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(299): Show | 337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.403+3718C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222744 | ||||||
| chr4:4222816
|
C | T | 1 | a0002c0002t0001g0298 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.403+3646G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222816 | ||||||
| chr4:4222986
|
T | A | 128 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(125): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.403+3476A>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4222986 | ||||||
| chr4:4223014
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.403+3448C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223014 | ||||||
| chr4:4223099
|
A | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3363T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223099 | ||||||
| chr4:4223197
|
C | T | 1 | a0009c0018t0001g0035 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.403+3265G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223197 | ||||||
| chr4:4223216
|
T | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3246A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223216 | ||||||
| chr4:4223408
|
CAGAT | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3050_403+3053d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223408 | ||||||
| chr4:4223409
|
A | AGATG | 220 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(217): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.403+3049_403+3052d others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | ||||||
| chr4:4223409
|
A | AGATGGAT others(1): Show |
62 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(59): Show | 69 | HG00621.hp1 HG01433.hp2 HG01891.hp2 others(66): Show |
intron_variant | MODIFIER | c.403+3045_403+3052d others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | ||||||
| chr4:4223409
|
A | AGATGGAT others(5): Show |
2 | a0001c0001t0001g0204a0001c0001t0001g0205 | 2 | HG02015.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.403+3041_403+3052d others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | ||||||
| chr4:4223409
|
A | AGATGGAT others(9): Show |
1 | a0008c0009t0001g0380 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.403+3037_403+3052d others(18): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | ||||||
| chr4:4223409
|
AGATGGAT others(1): Show |
A | 3 | a0001c0001t0001g0216a0002c0002t0001g0215a0002c0002t0001g0333 | 3 | HG00544.hp1 NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.403+3045_403+3052d others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223409 | ||||||
| chr4:4223441
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3021C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223441 | ||||||
| chr4:4223443
|
A | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3019T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223443 | ||||||
| chr4:4223444
|
T | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+3018A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223444 | ||||||
| chr4:4223522
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+2940C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223522 | ||||||
| chr4:4223558
|
A | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0113a0001c0001t0001g0114others(8): Show | 12 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.403+2904T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223558 | ||||||
| chr4:4223572
|
G | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+2890C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223572 | ||||||
| chr4:4223578
|
C | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(297): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.403+2884G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223578 | ||||||
| chr4:4223622
|
G | A | 1 | a0008c0009t0001g0365 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.403+2840C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223622 | ||||||
| chr4:4223634
|
C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(297): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.403+2828G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223634 | ||||||
| chr4:4223757
|
T | G | 1 | a0002c0002t0001g0090 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.403+2705A>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223757 | ||||||
| chr4:4223769
|
C | T | 1 | a0002c0002t0001g0295 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.403+2693G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223769 | ||||||
| chr4:4223800
|
G | A | 1 | a0008c0009t0001g0364 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.403+2662C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223800 | ||||||
| chr4:4223888
|
TCAAAAA | T | 122 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.403+2568_403+2573d others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4223888 | ||||||
| chr4:4224050
|
A | C | 1 | a0009c0012t0001g0195 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.403+2412T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224050 | ||||||
| chr4:4224219
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG00280.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.403+2243G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224219 | ||||||
| chr4:4224271
|
C | T | 1 | a0001c0004t0001g0250 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.403+2191G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224271 | ||||||
| chr4:4224278
|
T | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+2184A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224278 | ||||||
| chr4:4224280
|
G | A | 1 | a0001c0004t0001g0246 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.403+2182C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224280 | ||||||
| chr4:4224288
|
A | G | 10 | a0001c0001t0001g0010a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG00738.hp1 HG02004.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.403+2174T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224288 | ||||||
| chr4:4224346
|
C | CA | 33 | a0001c0001t0001g0130a0001c0001t0001g0145a0001c0001t0001g0146others(30): Show | 33 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.403+2115dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224346 | ||||||
| chr4:4224346
|
C | CAA | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0012others(58): Show | 70 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.403+2114_403+2115d others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224346 | ||||||
| chr4:4224389
|
C | G | 38 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(35): Show | 38 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.403+2073G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224389 | ||||||
| chr4:4224620
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.403+1842T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224620 | ||||||
| chr4:4224642
|
C | CTAAAACA others(5): Show |
1 | a0001c0004t0001g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.403+1808_403+1819d others(14): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224642 | ||||||
| chr4:4224764
|
G | A | 33 | a0001c0001t0001g0015a0001c0001t0001g0113a0001c0001t0001g0114others(30): Show | 34 | HG00733.hp2 HG01167.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.403+1698C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224764 | ||||||
| chr4:4224821
|
G | A | 3 | a0008c0009t0001g0367a0011c0014t0001g0366a0011c0014t0001g0368 | 3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+1641C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224821 | ||||||
| chr4:4224835
|
G | A | 1 | a0001c0004t0001g0247 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.403+1627C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224835 | ||||||
| chr4:4224853
|
G | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(138): Show | 156 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.403+1609C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224853 | ||||||
| chr4:4224854
|
AAGTGAGG others(3): Show |
A | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(138): Show | 156 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.403+1598_403+1607d others(12): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224854 | ||||||
| chr4:4224885
|
G | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(289): Show | 327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.403+1577C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224885 | ||||||
| chr4:4224976
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(290): Show | 330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.403+1486A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4224976 | ||||||
| chr4:4225232
|
G | A | 2 | a0012c0015t0001g0381a0012c0015t0001g0382 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.403+1230C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225232 | ||||||
| chr4:4225296
|
A | C | 3 | a0002c0002t0001g0291a0002c0002t0001g0293a0002c0020t0001g0292 | 3 | HG01981.hp2 NA18941.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.403+1166T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225296 | ||||||
| chr4:4225297
|
C | T | 2 | a0012c0015t0001g0381a0012c0015t0001g0382 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.403+1165G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225297 | ||||||
| chr4:4225338
|
G | A | 1 | a0002c0003t0001g0227 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.403+1124C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225338 | ||||||
| chr4:4225413
|
A | T | 1 | a0001c0001t0001g0290 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.403+1049T>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225413 | ||||||
| chr4:4225456
|
C | A | 5 | a0001c0001t0001g0193a0007c0010t0001g0379a0008c0009t0001g0377others(2): Show | 5 | HG01109.hp1 HG02809.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+1006G>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225456 | ||||||
| chr4:4225560
|
T | C | 1 | a0002c0002t0001g0141 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.403+902A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225560 | ||||||
| chr4:4225566
|
C | CA | 17 | a0001c0001t0001g0198a0001c0001t0001g0353a0001c0001t0001g0354others(14): Show | 17 | HG00597.hp2 HG01081.hp1 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.403+895dupT | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225566
|
C | CAA | 35 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(32): Show | 40 | HG00621.hp1 HG00733.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.403+894_403+895dup others(2): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225566
|
C | CAAA | 9 | a0001c0001t0001g0220a0001c0004t0001g0190a0002c0002t0001g0141others(6): Show | 9 | HG02622.hp1 HG03654.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.403+893_403+895dup others(3): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225566
|
C | CAAAA | 28 | a0001c0001t0001g0019a0001c0001t0001g0046a0001c0001t0001g0191others(25): Show | 29 | HG00738.hp1 HG01192.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.403+892_403+895dup others(4): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225566
|
C | CAAAAA | 35 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0049others(32): Show | 39 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.403+891_403+895dup others(5): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225566
|
C | CAAAAAA | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(135): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.403+890_403+895dup others(6): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225566
|
C | CAAAAAAA | 37 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0020others(34): Show | 41 | HG00544.hp2 HG00673.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.403+889_403+895dup others(7): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225566
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(5): Show | 8 | HG02080.hp1 HG02895.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.403+888_403+895dup others(8): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225566
|
C | CAAAAAAA others(2): Show |
6 | a0002c0003t0001g0126a0002c0003t0001g0128a0004c0006t0001g0124others(3): Show | 6 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.403+887_403+895dup others(9): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225566
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0130 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.403+886_403+895dup others(10): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225566 | ||||||
| chr4:4225667
|
C | G | 3 | a0008c0009t0001g0367a0011c0014t0001g0366a0011c0014t0001g0368 | 3 | HG01891.hp2 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.403+795G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225667 | ||||||
| chr4:4225691
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0182 | 5 | HG00735.hp2 HG01884.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.403+771C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225691 | ||||||
| chr4:4225711
|
A | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(273): Show | 312 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.403+751T>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225711 | ||||||
| chr4:4225713
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.403+749G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225713 | ||||||
| chr4:4225717
|
T | C | 1 | a0001c0004t0001g0107 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.403+745A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225717 | ||||||
| chr4:4225730
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.403+732T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225730 | ||||||
| chr4:4225828
|
C | G | 1 | a0002c0002t0001g0196 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.403+634G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225828 | ||||||
| chr4:4225848
|
T | C | 1 | a0001c0004t0001g0250 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.403+614A>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225848 | ||||||
| chr4:4225854
|
C | T | 1 | a0001c0004t0001g0250 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.403+608G>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225854 | ||||||
| chr4:4225916
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.403+546C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4225916 | ||||||
| chr4:4226038
|
G | T | 1 | a0008c0009t0001g0365 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.403+424C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226038 | ||||||
| chr4:4226047
|
C | G | 2 | a0001c0001t0001g0139a0003c0005t0001g0138 | 2 | HG00544.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.403+415G>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226047 | ||||||
| chr4:4226048
|
G | C | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0359 | 3 | HG02451.hp2 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.403+414C>G | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226048 | ||||||
| chr4:4226110
|
G | A | 157 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(154): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.403+352C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226110 | ||||||
| chr4:4226281
|
A | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(195): Show | 215 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.403+181T>C | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226281 | ||||||
| chr4:4226301
|
G | T | 83 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0016others(80): Show | 89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.403+161C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226301 | ||||||
| chr4:4226302
|
A | AAAG | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(257): Show | 289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.403+157_403+159dup others(3): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226302 | ||||||
| chr4:4226335
|
G | T | 82 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(79): Show | 91 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.403+127C>A | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226335 | ||||||
| chr4:4226366
|
G | GGGAAGAC others(26): Show |
1 | a0001c0001t0001g0359 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.403+63_403+95dupTG others(31): Show |
OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226366 | ||||||
| chr4:4226447
|
G | A | 2 | a0001c0001t0001g0360a0002c0002t0001g0361 | 2 | HG03490.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.403+15C>T | OTOP1 | ENSG00000163982.6 | transcript | ENST00000296358.5 | protein_coding | 1/5 | chr4 | 4226447 |