Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 285533 |
|---|---|
| ensemblid | ENSG00000145428.15 |
| hgncid | 27735 |
| symbol | RNF175 |
| name | ring finger protein 175 |
| refseq_nuc | NM_173662.4 |
| refseq_prot | NP_775933.2 |
| ensembl_nuc | ENST00000347063.9 |
| ensembl_prot | ENSP00000340979.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 153710160 |
| end | 153760024 |
| strand | - |
| ver | v1.2 |
| region | chr4:153710160-153760024 |
| region5000 | chr4:153705160-153765024 |
| regionname0 | RNF175_chr4_153710160_153760024 |
| regionname5000 | RNF175_chr4_153705160_153765024 |
| 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 | 328 | 227 | 66 | 30 | 102 | 8 | 21 | 82 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0002 | 0/0 | 328 | 67 | 0 | 12 | 49 | 4 | 2 | 37 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0003 | 0/0 | 328 | 58 | 3 | 4 | 44 | 0 | 7 | 36 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0004 | 0/0 | 328 | 17 | 0 | 9 | 0 | 2 | 6 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0005 | 1/0 | 328 | 12 | 9 | 1 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0006 | 0/1 | 328 | 3 | 0 | 1 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0007 | 0/0 | 328 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0008 | 0/0 | 328 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0009 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0010 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0011 | 0/0 | 328 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0012 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0013 | 0/0 | 328 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0014 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| 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 | 987 | 227 | 66 | 30 | 102 | 8 | 21 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0002 | 0/0 | 987 | 67 | 0 | 12 | 49 | 4 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0003 | 0/0 | 987 | 58 | 3 | 4 | 44 | 0 | 7 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0004 | 0/0 | 987 | 17 | 0 | 9 | 0 | 2 | 6 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0005 | 1/0 | 987 | 12 | 9 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0006 | 0/1 | 987 | 3 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0007 | 0/0 | 987 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0008 | 0/0 | 987 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0009 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0010 | 0/0 | 987 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0011 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0012 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0013 | 0/0 | 987 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| c0014 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| 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 | 372 | 392 | 84 | 58 | 195 | 14 | 39 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| t0002 | 0/0 | 372 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| t0003 | 0/0 | 372 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| 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 | 10 | 0 | 0 | 10 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0003 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0004 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0009 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0017 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| 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 | 987 | 227 | 66 | 30 | 102 | 8 | 21 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0002c0002 | 0/0 | 987 | 67 | 0 | 12 | 49 | 4 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0003c0003 | 0/0 | 987 | 58 | 3 | 4 | 44 | 0 | 7 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0004c0004 | 0/0 | 987 | 17 | 0 | 9 | 0 | 2 | 6 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0005c0005 | 1/0 | 987 | 12 | 9 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0006c0006 | 0/1 | 987 | 3 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0007c0007 | 0/0 | 987 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0008c0008 | 0/0 | 987 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0009c0011 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0010c0012 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0011c0013 | 0/0 | 987 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0012c0014 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0013c0010 | 0/0 | 987 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0014c0009 | 0/0 | 987 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1358 | 226 | 66 | 30 | 102 | 8 | 20 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0001c0001t0003 | 0/0 | 1358 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0002c0002t0001 | 0/0 | 1358 | 66 | 0 | 12 | 48 | 4 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0002c0002t0002 | 0/0 | 1358 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0003c0003t0001 | 0/0 | 1358 | 58 | 3 | 4 | 44 | 0 | 7 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0004c0004t0001 | 0/0 | 1358 | 17 | 0 | 9 | 0 | 2 | 6 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0005c0005t0001 | 1/0 | 1358 | 12 | 9 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0006c0006t0001 | 0/1 | 1358 | 3 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0007c0007t0001 | 0/0 | 1358 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0008c0008t0001 | 0/0 | 1358 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0009c0011t0001 | 0/0 | 1358 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0010c0012t0001 | 0/0 | 1358 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0011c0013t0001 | 0/0 | 1358 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0012c0014t0001 | 0/0 | 1358 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0013c0010t0001 | 0/0 | 1358 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| a0014c0009t0001 | 0/0 | 1358 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | copy fasta | chr4 | 153705160 | 153765024 |
| 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 | 10 | 0 | 0 | 10 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0017 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0004 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0003 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0006c0006t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0006c0006t0001g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0007c0007t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0007c0007t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0008c0008t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0008c0008t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0009c0011t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0010c0012t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0011c0013t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0012c0014t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0013c0010t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0014c0009t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0004 | t0001 | g0291 | EUR | GBR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0156 | EUR | FIN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00323 | hp1 | a0004 | c0004 | t0001 | g0290 | EUR | FIN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0113 | EUR | FIN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00558 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0065 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0023 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0051 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01081 | hp1 | a0013 | c0010 | t0001 | g0050 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0028 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01243 | hp1 | a0004 | c0004 | t0001 | g0298 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01243 | hp2 | a0005 | c0005 | t0001 | g0286 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01257 | hp2 | a0004 | c0004 | t0001 | g0297 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01346 | hp2 | a0006 | c0006 | t0001 | g0042 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01358 | hp1 | a0004 | c0004 | t0001 | g0233 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0102 | EUR | IBS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01891 | hp2 | a0007 | c0007 | t0001 | g0289 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01928 | hp1 | a0004 | c0004 | t0001 | g0296 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01952 | hp2 | a0004 | c0004 | t0001 | g0010 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01981 | hp1 | a0004 | c0004 | t0001 | g0010 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02040 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02055 | hp1 | a0010 | c0012 | t0001 | g0255 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02148 | hp1 | a0004 | c0004 | t0001 | g0010 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0054 | EAS | CDX | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CDX | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02273 | hp2 | a0004 | c0004 | t0001 | g0295 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02300 | hp2 | a0004 | c0004 | t0001 | g0043 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0077 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02572 | hp2 | a0005 | c0005 | t0001 | g0194 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0071 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02683 | hp1 | a0004 | c0004 | t0001 | g0010 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02698 | hp2 | a0004 | c0004 | t0001 | g0299 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02735 | hp1 | a0004 | c0004 | t0001 | g0043 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0003 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02922 | hp1 | a0005 | c0005 | t0001 | g0196 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02970 | hp1 | a0005 | c0005 | t0001 | g0032 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03017 | hp1 | a0006 | c0006 | t0001 | g0042 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03098 | hp2 | a0005 | c0005 | t0001 | g0197 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03130 | hp2 | a0005 | c0005 | t0001 | g0210 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03209 | hp1 | a0012 | c0014 | t0001 | g0288 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0070 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03225 | hp2 | a0014 | c0009 | t0001 | g0046 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03453 | hp2 | a0007 | c0007 | t0001 | g0206 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03486 | hp2 | a0005 | c0005 | t0001 | g0032 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03490 | hp2 | a0003 | c0003 | t0001 | g0049 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03491 | hp2 | a0008 | c0008 | t0001 | g0114 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0048 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03492 | hp2 | a0008 | c0008 | t0001 | g0115 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03579 | hp2 | a0005 | c0005 | t0001 | g0203 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0225 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0306 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0074 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04184 | hp2 | a0004 | c0004 | t0001 | g0294 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0023 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04228 | hp1 | a0005 | c0005 | t0001 | g0202 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0057 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | CHB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18949 | hp1 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18960 | hp1 | a0003 | c0003 | t0001 | g0075 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0063 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0076 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18972 | hp2 | a0003 | c0003 | t0001 | g0055 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18977 | hp2 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0069 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0080 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0078 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0056 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0079 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19030 | hp1 | a0005 | c0005 | t0001 | g0207 | AFR | LWK | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19054 | hp1 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0059 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19063 | hp1 | a0003 | c0003 | t0001 | g0011 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19065 | hp2 | a0011 | c0013 | t0001 | g0180 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19072 | hp1 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0068 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ASW | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20129 | hp2 | a0005 | c0005 | t0001 | g0205 | AFR | ASW | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0092 | EUR | TSI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | GIH | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20905 | hp2 | a0004 | c0004 | t0001 | g0292 | SAS | GIH | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0045 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02559 | hp2 | a0009 | c0011 | t0001 | g0230 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | USA | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18955 | hp1 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| homoSapiens_chm13v2 | hp1 | a0006 | c0006 | t0001 | g0300 | REF | REF | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| homoSapiens_grch38 | hp1 | a0005 | c0005 | t0001 | g0145 | REF | REF | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153710391
|
A | T | 12 | a0001a0002a0003others(9): Show | 380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
missense_variant | MODERATE | c.965T>A | p.Ile322Asn | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 9/9 | 1127/1358 | 965/987 | 322/328 | chr4 | 153710391 | ||
| chr4:153710398
|
C | T | 1 | a0012 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.958G>A | p.Gly320Ser | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 9/9 | 1120/1358 | 958/987 | 320/328 | chr4 | 153710398 | ||
| chr4:153710411
|
T | C | 2 | a0002a0008 | 69 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(66): Show |
missense_variant | MODERATE | c.945A>G | p.Ile315Met | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 9/9 | 1107/1358 | 945/987 | 315/328 | chr4 | 153710411 | ||
| chr4:153710435
|
C | G | 1 | a0004 | 17 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(14): Show |
missense_variant | MODERATE | c.921G>C | p.Leu307Phe | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 9/9 | 1083/1358 | 921/987 | 307/328 | chr4 | 153710435 | ||
| chr4:153715537
|
A | C | 1 | a0013 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.756T>G | p.Cys252Trp | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/9 | 918/1358 | 756/987 | 252/328 | chr4 | 153715537 | ||
| chr4:153715580
|
A | G | 1 | a0014 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.713T>C | p.Leu238Pro | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/9 | 875/1358 | 713/987 | 238/328 | chr4 | 153715580 | ||
| chr4:153715646
|
C | T | 1 | a0007 | 2 | HG01891.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.647G>A | p.Arg216Gln | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/9 | 809/1358 | 647/987 | 216/328 | chr4 | 153715646 | ||
| chr4:153723385
|
T | C | 2 | a0004a0006 | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
missense_variant | MODERATE | c.475A>G | p.Met159Val | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/9 | 637/1358 | 475/987 | 159/328 | chr4 | 153723385 | ||
| chr4:153723390
|
G | A | 1 | a0008 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.470C>T | p.Ala157Val | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/9 | 632/1358 | 470/987 | 157/328 | chr4 | 153723390 | ||
| chr4:153728207
|
C | T | 1 | a0011 | 1 | NA19065.hp2 | missense_variant&splice_region_variant | MODERATE | c.401G>A | p.Arg134Gln | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/9 | 563/1358 | 401/987 | 134/328 | chr4 | 153728207 | ||
| chr4:153748707
|
C | T | 1 | a0010 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.184G>A | p.Val62Ile | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/9 | 346/1358 | 184/987 | 62/328 | chr4 | 153748707 | ||
| chr4:153748734
|
C | G | 1 | a0009 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.157G>C | p.Val53Leu | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/9 | 319/1358 | 157/987 | 53/328 | chr4 | 153748734 | ||
| chr4:153759802
|
C | T | 3 | a0003a0013a0014 | 60 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
missense_variant | MODERATE | c.61G>A | p.Glu21Lys | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/9 | 223/1358 | 61/987 | 21/328 | chr4 | 153759802 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153759879
|
C | T | 1 | a0002c0002t0002 | 1 | NA18940.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/9 | 17 | chr4 | 153759879 | |||||
| chr4:153760016
|
G | A | 1 | a0001c0001t0003 | 1 | HG03688.hp1 | 5_prime_UTR_variant | MODIFIER | c.-154C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/9 | 154 | chr4 | 153760016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153710851
|
G | A | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039others(5): Show | 11 | HG00408.hp1 HG00609.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.867-362C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153710851 | ||||||
| chr4:153710910
|
A | G | 74 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(71): Show | 95 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.867-421T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153710910 | ||||||
| chr4:153711397
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.867-908C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711397 | ||||||
| chr4:153711454
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(56): Show | 81 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.867-965T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711454 | ||||||
| chr4:153711686
|
G | A | 27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(24): Show | 32 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.866+789C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711686 | ||||||
| chr4:153711735
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.866+740T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711735 | ||||||
| chr4:153711795
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG00408.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.866+680T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711795 | ||||||
| chr4:153711807
|
C | A | 1 | a0002c0002t0001g0127 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.866+668G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711807 | ||||||
| chr4:153711843
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(290): Show | 380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.866+632G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711843 | ||||||
| chr4:153711846
|
C | G | 1 | a0001c0001t0001g0035 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.866+629G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711846 | ||||||
| chr4:153712131
|
C | G | 1 | a0001c0001t0001g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.866+344G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153712131 | ||||||
| chr4:153712428
|
GA | G | 78 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(75): Show | 100 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.866+46delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153712428 | ||||||
| chr4:153712582
|
G | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 99 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
splice_region_variant&intron_variant | LOW | c.765-6C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153712582 | ||||||
| chr4:153712695
|
C | T | 1 | a0003c0003t0001g0058 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.765-119G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153712695 | ||||||
| chr4:153712853
|
C | CT | 28 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(25): Show | 33 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.765-278dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153712853 | ||||||
| chr4:153713123
|
A | C | 52 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(49): Show | 66 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.765-547T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713123 | ||||||
| chr4:153713266
|
T | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.765-690A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713266 | ||||||
| chr4:153713351
|
T | A | 1 | a0002c0002t0001g0100 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.765-775A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713351 | ||||||
| chr4:153713583
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.765-1007T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713583 | ||||||
| chr4:153713765
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.765-1189T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713765 | ||||||
| chr4:153713836
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.765-1260G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713836 | ||||||
| chr4:153713852
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.765-1276C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713852 | ||||||
| chr4:153713877
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(290): Show | 380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.765-1301A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713877 | ||||||
| chr4:153713963
|
T | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(206): Show | 272 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(269): Show |
intron_variant | MODIFIER | c.765-1387A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713963 | ||||||
| chr4:153713971
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.765-1395C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713971 | ||||||
| chr4:153714156
|
A | G | 1 | a0003c0003t0001g0067 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.764+1373T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714156 | ||||||
| chr4:153714192
|
G | A | 2 | a0002c0002t0001g0092a0002c0002t0001g0093 | 2 | HG01099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.764+1337C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714192 | ||||||
| chr4:153714284
|
C | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(71): Show | 101 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.764+1245G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714284 | ||||||
| chr4:153714445
|
C | T | 1 | a0007c0007t0001g0206 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.764+1084G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714445 | ||||||
| chr4:153714474
|
A | G | 7 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0195others(4): Show | 9 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.764+1055T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714474 | ||||||
| chr4:153714620
|
C | T | 1 | a0002c0002t0001g0156 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.764+909G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714620 | ||||||
| chr4:153714698
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.764+831C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714698 | ||||||
| chr4:153714864
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.764+665A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714864 | ||||||
| chr4:153714877
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.764+652C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714877 | ||||||
| chr4:153714887
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 100 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.764+642G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714887 | ||||||
| chr4:153715004
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.764+525T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715004 | ||||||
| chr4:153715011
|
C | A | 1 | a0001c0001t0001g0038 | 2 | HG01975.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.764+518G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715011 | ||||||
| chr4:153715098
|
T | A | 1 | a0001c0001t0001g0245 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.764+431A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715098 | ||||||
| chr4:153715167
|
A | G | 1 | a0003c0003t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.764+362T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715167 | ||||||
| chr4:153715374
|
A | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0216a0003c0003t0001g0045 | 4 | HG02109.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.764+155T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715374 | ||||||
| chr4:153715924
|
T | C | 1 | a0005c0005t0001g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.631-262A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153715924 | ||||||
| chr4:153715927
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.631-265C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153715927 | ||||||
| chr4:153715978
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-316G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153715978 | ||||||
| chr4:153716048
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-386T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716048 | ||||||
| chr4:153716054
|
ACT | A | 72 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 93 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.631-394_631-393del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716054 | ||||||
| chr4:153716063
|
C | CA | 63 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0033others(60): Show | 78 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.631-402dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716063 | ||||||
| chr4:153716063
|
CA | C | 85 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(82): Show | 110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.631-402delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716063 | ||||||
| chr4:153716063
|
CAA | C | 53 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(50): Show | 75 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.631-403_631-402del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716063 | ||||||
| chr4:153716063
|
CAAAAAAA others(6): Show |
C | 15 | a0004c0004t0001g0010a0004c0004t0001g0043a0004c0004t0001g0225others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.631-414_631-402del others(13): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716063 | ||||||
| chr4:153716107
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-445T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716107 | ||||||
| chr4:153716109
|
A | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0216a0003c0003t0001g0045 | 4 | HG02109.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-447T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716109 | ||||||
| chr4:153716128
|
C | T | 1 | a0002c0002t0001g0130 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.631-466G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716128 | ||||||
| chr4:153716236
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.631-574G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716236 | ||||||
| chr4:153716399
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-737C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716399 | ||||||
| chr4:153716555
|
C | G | 1 | a0001c0001t0001g0135 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.631-893G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716555 | ||||||
| chr4:153716612
|
C | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 80 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.631-950G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716612 | ||||||
| chr4:153716643
|
C | A | 6 | a0003c0003t0001g0011a0003c0003t0001g0026a0003c0003t0001g0058others(3): Show | 9 | HG02135.hp2 NA18942.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.631-981G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716643 | ||||||
| chr4:153716694
|
A | G | 1 | a0003c0003t0001g0065 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.631-1032T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716694 | ||||||
| chr4:153716730
|
G | A | 7 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 7 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.631-1068C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716730 | ||||||
| chr4:153716742
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 6 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-1080C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716742 | ||||||
| chr4:153716850
|
G | A | 7 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 7 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.631-1188C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716850 | ||||||
| chr4:153716855
|
T | C | 1 | a0003c0003t0001g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.631-1193A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716855 | ||||||
| chr4:153716933
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0216a0003c0003t0001g0045 | 4 | HG02109.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-1271G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716933 | ||||||
| chr4:153716962
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-1300T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716962 | ||||||
| chr4:153716969
|
G | T | 15 | a0004c0004t0001g0010a0004c0004t0001g0043a0004c0004t0001g0225others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.631-1307C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716969 | ||||||
| chr4:153716974
|
T | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(72): Show | 102 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.631-1312A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716974 | ||||||
| chr4:153717013
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-1351G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717013 | ||||||
| chr4:153717049
|
G | C | 1 | a0001c0001t0001g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.631-1387C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717049 | ||||||
| chr4:153717465
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.631-1803C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717465 | ||||||
| chr4:153717483
|
A | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.631-1821T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717483 | ||||||
| chr4:153717507
|
T | G | 1 | a0002c0002t0001g0107 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.631-1845A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717507 | ||||||
| chr4:153717534
|
A | AAC | 142 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(139): Show | 188 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.631-1874_631-1873d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | ||||||
| chr4:153717534
|
A | AACAC | 59 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0085others(56): Show | 73 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.631-1876_631-1873d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | ||||||
| chr4:153717534
|
A | AACACAC | 27 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(24): Show | 32 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.631-1878_631-1873d others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | ||||||
| chr4:153717534
|
A | C | 5 | a0001c0001t0001g0031a0001c0001t0001g0168a0001c0001t0001g0182others(2): Show | 6 | HG03704.hp1 HG03710.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-1872T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | ||||||
| chr4:153717534
|
AAC | A | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0146 | 3 | HG02055.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.631-1874_631-1873d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | ||||||
| chr4:153717590
|
T | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-1928A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717590 | ||||||
| chr4:153717775
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0216a0003c0003t0001g0045 | 4 | HG02109.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-2113A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717775 | ||||||
| chr4:153717903
|
G | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-2241C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717903 | ||||||
| chr4:153717944
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.630+2240T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717944 | ||||||
| chr4:153717953
|
G | A | 15 | a0004c0004t0001g0010a0004c0004t0001g0043a0004c0004t0001g0225others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.630+2231C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717953 | ||||||
| chr4:153717953
|
G | T | 12 | a0005c0005t0001g0032a0005c0005t0001g0194a0005c0005t0001g0196others(9): Show | 13 | HG01243.hp2 HG01891.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.630+2231C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717953 | ||||||
| chr4:153718054
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.630+2130A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718054 | ||||||
| chr4:153718208
|
AGTTTTTT others(22): Show |
A | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.630+1947_630+1975d others(31): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718208 | ||||||
| chr4:153718214
|
TTTTG | T | 69 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(66): Show | 89 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.630+1966_630+1969d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718214 | ||||||
| chr4:153718214
|
TTTTGTTT others(1): Show |
T | 5 | a0005c0005t0001g0197a0005c0005t0001g0202a0005c0005t0001g0210others(2): Show | 5 | HG01891.hp2 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+1962_630+1969d others(10): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718214 | ||||||
| chr4:153718218
|
G | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(57): Show | 82 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.630+1966C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718218 | ||||||
| chr4:153718222
|
G | GT | 45 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(42): Show | 64 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.630+1961dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | ||||||
| chr4:153718222
|
G | GTTTTGT | 14 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0041others(11): Show | 17 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.630+1961_630+1962i others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | ||||||
| chr4:153718222
|
G | GTTTTTTT others(2): Show |
10 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0154others(7): Show | 13 | HG00099.hp2 HG01515.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.630+1961_630+1962i others(11): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | ||||||
| chr4:153718222
|
G | GTTTTTTT others(3): Show |
5 | a0001c0001t0001g0016a0001c0001t0001g0235a0001c0001t0001g0244others(2): Show | 7 | HG00280.hp1 HG00738.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.630+1961_630+1962i others(12): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | ||||||
| chr4:153718222
|
G | GTTTTTTT others(4): Show |
4 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0238others(1): Show | 4 | HG01192.hp2 HG01261.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1961_630+1962i others(13): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | ||||||
| chr4:153718222
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0152 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.630+1961_630+1962i others(14): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | ||||||
| chr4:153718222
|
G | GTTTTTTT others(6): Show |
1 | a0009c0011t0001g0230 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.630+1961_630+1962i others(15): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | ||||||
| chr4:153718223
|
TTTG | T | 63 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(60): Show | 82 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.630+1958_630+1960d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718223 | ||||||
| chr4:153718223
|
TTTGTTTG | T | 7 | a0005c0005t0001g0032a0005c0005t0001g0194a0005c0005t0001g0196others(4): Show | 8 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.630+1954_630+1960d others(9): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718223 | ||||||
| chr4:153718223
|
TTTGTTTG others(4): Show |
T | 12 | a0004c0004t0001g0010a0004c0004t0001g0043a0004c0004t0001g0225others(9): Show | 17 | HG00323.hp1 HG01243.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.630+1950_630+1960d others(13): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718223 | ||||||
| chr4:153718224
|
TTG | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0083a0001c0001t0001g0186others(12): Show | 18 | HG00423.hp1 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.630+1958_630+1959d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718224 | ||||||
| chr4:153718224
|
TTGTTTG | T | 5 | a0002c0002t0001g0104a0002c0002t0001g0108a0002c0002t0001g0112others(2): Show | 5 | HG00423.hp2 HG03017.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+1954_630+1959d others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718224 | ||||||
| chr4:153718224
|
TTGTTTGT others(3): Show |
T | 2 | a0004c0004t0001g0291a0004c0004t0001g0299 | 2 | HG00099.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.630+1950_630+1959d others(12): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718224 | ||||||
| chr4:153718225
|
TGTTTG | T | 30 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(27): Show | 43 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.630+1954_630+1958d others(7): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718225 | ||||||
| chr4:153718226
|
G | T | 30 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(27): Show | 35 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.630+1958C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718226 | ||||||
| chr4:153718227
|
T | TTTTG | 28 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0031others(25): Show | 41 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.630+1956_630+1957i others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718227 | ||||||
| chr4:153718227
|
TTTGTTTG others(4): Show |
T | 1 | a0004c0004t0001g0294 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.630+1946_630+1956d others(13): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718227 | ||||||
| chr4:153718228
|
T | TTTG | 15 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0030others(12): Show | 21 | HG01081.hp2 HG01884.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.630+1955_630+1956i others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718228 | ||||||
| chr4:153718230
|
G | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(234): Show | 306 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.630+1954C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718230 | ||||||
| chr4:153718234
|
G | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 368 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(365): Show |
intron_variant | MODIFIER | c.630+1950C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718234 | ||||||
| chr4:153718238
|
G | T | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.630+1946C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718238 | ||||||
| chr4:153718253
|
G | T | 130 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0018others(127): Show | 166 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.630+1931C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718253 | ||||||
| chr4:153718294
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.630+1890G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718294 | ||||||
| chr4:153718365
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.630+1819G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718365 | ||||||
| chr4:153718515
|
T | G | 72 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 93 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.630+1669A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718515 | ||||||
| chr4:153718522
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.630+1662C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718522 | ||||||
| chr4:153718795
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+1389G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718795 | ||||||
| chr4:153718878
|
C | A | 4 | a0001c0001t0001g0147a0001c0001t0001g0212a0001c0001t0001g0213others(1): Show | 4 | HG02723.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1306G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718878 | ||||||
| chr4:153719011
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+1173G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719011 | ||||||
| chr4:153719114
|
G | A | 95 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(92): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.630+1070C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719114 | ||||||
| chr4:153719177
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.630+1007G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719177 | ||||||
| chr4:153719209
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.630+975T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719209 | ||||||
| chr4:153719337
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.630+847A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719337 | ||||||
| chr4:153719379
|
G | A | 73 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(70): Show | 94 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.630+805C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719379 | ||||||
| chr4:153719405
|
A | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(75): Show | 99 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.630+779T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719405 | ||||||
| chr4:153719627
|
C | A | 2 | a0003c0003t0001g0053a0003c0003t0001g0061 | 2 | HG00423.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.630+557G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719627 | ||||||
| chr4:153719700
|
A | T | 106 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(103): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+484T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719700 | ||||||
| chr4:153719739
|
T | C | 34 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(31): Show | 40 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.630+445A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719739 | ||||||
| chr4:153719758
|
C | A | 1 | a0005c0005t0001g0203 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.630+426G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719758 | ||||||
| chr4:153719781
|
G | A | 106 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(103): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+403C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719781 | ||||||
| chr4:153719790
|
A | G | 106 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(103): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+394T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719790 | ||||||
| chr4:153719791
|
C | A | 106 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(103): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+393G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719791 | ||||||
| chr4:153719920
|
G | A | 106 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(103): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.630+264C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719920 | ||||||
| chr4:153719922
|
A | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0215a0001c0001t0001g0284 | 4 | HG02451.hp1 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+262T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719922 | ||||||
| chr4:153719971
|
A | T | 15 | a0004c0004t0001g0010a0004c0004t0001g0043a0004c0004t0001g0225others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.630+213T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719971 | ||||||
| chr4:153719998
|
G | T | 90 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(87): Show | 115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.630+186C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719998 | ||||||
| chr4:153720337
|
T | C | 106 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(103): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.510-33A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720337 | ||||||
| chr4:153720389
|
A | C | 1 | a0001c0001t0001g0120 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.510-85T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720389 | ||||||
| chr4:153720413
|
T | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0229a0001c0001t0001g0231 | 3 | HG02818.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.510-109A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720413 | ||||||
| chr4:153720426
|
ATG | A | 74 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(71): Show | 95 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.510-124_510-123del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720426 | ||||||
| chr4:153720486
|
T | C | 62 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0040others(59): Show | 77 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.510-182A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720486 | ||||||
| chr4:153720521
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.510-217A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720521 | ||||||
| chr4:153720538
|
T | A | 72 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(69): Show | 93 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.510-234A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720538 | ||||||
| chr4:153720576
|
G | A | 1 | a0002c0002t0001g0097 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.510-272C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720576 | ||||||
| chr4:153720917
|
C | T | 2 | a0003c0003t0001g0048a0003c0003t0001g0049 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.510-613G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720917 | ||||||
| chr4:153721085
|
T | A | 2 | a0007c0007t0001g0206a0007c0007t0001g0289 | 2 | HG01891.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.510-781A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721085 | ||||||
| chr4:153721120
|
A | G | 70 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(67): Show | 91 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.510-816T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721120 | ||||||
| chr4:153721149
|
C | T | 55 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0040others(52): Show | 70 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.510-845G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721149 | ||||||
| chr4:153721157
|
GT | G | 132 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0018others(129): Show | 168 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.510-854delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721157 | ||||||
| chr4:153721546
|
T | C | 241 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0016others(238): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.510-1242A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721546 | ||||||
| chr4:153721583
|
G | C | 1 | a0001c0001t0001g0174 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510-1279C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721583 | ||||||
| chr4:153721682
|
G | A | 75 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(72): Show | 96 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.510-1378C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721682 | ||||||
| chr4:153721769
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.510-1465C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721769 | ||||||
| chr4:153722035
|
T | A | 2 | a0001c0001t0001g0040a0003c0003t0001g0045 | 3 | HG02109.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.509+1316A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722035 | ||||||
| chr4:153722070
|
G | T | 194 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(191): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.509+1281C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722070 | ||||||
| chr4:153722084
|
T | C | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 6 | HG00642.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+1267A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722084 | ||||||
| chr4:153722093
|
T | C | 15 | a0004c0004t0001g0010a0004c0004t0001g0043a0004c0004t0001g0225others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.509+1258A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722093 | ||||||
| chr4:153722225
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.509+1126G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722225 | ||||||
| chr4:153722234
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+1117C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722234 | ||||||
| chr4:153722351
|
G | A | 189 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(186): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.509+1000C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722351 | ||||||
| chr4:153722564
|
C | CAA | 50 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(47): Show | 69 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.509+785_509+786dup others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722564 | ||||||
| chr4:153722646
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.509+705C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722646 | ||||||
| chr4:153722648
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.509+703T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722648 | ||||||
| chr4:153722693
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.509+658C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722693 | ||||||
| chr4:153722703
|
C | T | 1 | a0012c0014t0001g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.509+648G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722703 | ||||||
| chr4:153722755
|
C | G | 1 | a0001c0001t0001g0262 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.509+596G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722755 | ||||||
| chr4:153722767
|
C | CA | 14 | a0001c0001t0001g0168a0001c0001t0001g0174a0001c0001t0001g0182others(11): Show | 14 | HG00323.hp2 HG00438.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.509+583dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722767 | ||||||
| chr4:153722767
|
CA | C | 55 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(52): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.509+583delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722767 | ||||||
| chr4:153722767
|
CAA | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0192a0001c0001t0001g0216others(2): Show | 6 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+582_509+583del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722767 | ||||||
| chr4:153722767
|
CAAA | C | 71 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(68): Show | 91 | HG00423.hp1 HG00733.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.509+581_509+583del others(3): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722767 | ||||||
| chr4:153722809
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.509+542T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722809 | ||||||
| chr4:153722848
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+503T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722848 | ||||||
| chr4:153723098
|
C | T | 99 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(96): Show | 126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.509+253G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153723098 | ||||||
| chr4:153723302
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.509+49A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153723302 | ||||||
| chr4:153723551
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.402-93G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153723551 | ||||||
| chr4:153723561
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.402-103A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153723561 | ||||||
| chr4:153723655
|
A | C | 79 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 102 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.402-197T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153723655 | ||||||
| chr4:153723777
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 216 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.402-319C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153723777 | ||||||
| chr4:153724029
|
G | C | 50 | a0001c0001t0001g0228a0002c0002t0001g0004a0002c0002t0001g0005others(47): Show | 69 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.402-571C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724029 | ||||||
| chr4:153724071
|
G | A | 19 | a0001c0001t0001g0040a0001c0001t0001g0192a0001c0001t0001g0216others(16): Show | 25 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.402-613C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724071 | ||||||
| chr4:153724159
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.402-701C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724159 | ||||||
| chr4:153724246
|
G | C | 1 | a0001c0001t0001g0272 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.402-788C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724246 | ||||||
| chr4:153724280
|
A | T | 1 | a0001c0001t0001g0119 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.402-822T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724280 | ||||||
| chr4:153724319
|
G | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 103 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.402-861C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724319 | ||||||
| chr4:153724322
|
C | T | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.402-864G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724322 | ||||||
| chr4:153724441
|
A | G | 15 | a0004c0004t0001g0010a0004c0004t0001g0043a0004c0004t0001g0225others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.402-983T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724441 | ||||||
| chr4:153724545
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(294): Show | 384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.402-1087C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724545 | ||||||
| chr4:153724564
|
C | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(294): Show | 384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.402-1106G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724564 | ||||||
| chr4:153724595
|
T | C | 297 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(294): Show | 384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.402-1137A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724595 | ||||||
| chr4:153724600
|
C | T | 1 | a0001c0001t0001g0301 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.402-1142G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724600 | ||||||
| chr4:153724658
|
T | C | 247 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(244): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.402-1200A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724658 | ||||||
| chr4:153724741
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.402-1283C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724741 | ||||||
| chr4:153724774
|
T | A | 59 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0152others(56): Show | 79 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.402-1316A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724774 | ||||||
| chr4:153724797
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402-1339A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724797 | ||||||
| chr4:153724909
|
C | T | 1 | a0002c0002t0001g0110 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.402-1451G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724909 | ||||||
| chr4:153724935
|
ACGTGGGG others(101): Show |
A | 1 | a0002c0002t0001g0155 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.402-1585_402-1478d others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724935 | ||||||
| chr4:153724962
|
A | ACGTGGGG others(47): Show |
5 | a0001c0001t0001g0125a0003c0003t0001g0054a0003c0003t0001g0064others(2): Show | 5 | HG00609.hp1 HG02155.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.402-1558_402-1505d others(56): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724962 | ||||||
| chr4:153724962
|
ACGTGGGG others(74): Show |
A | 49 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(46): Show | 68 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.402-1585_402-1505d others(83): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724962 | ||||||
| chr4:153724985
|
AGCTGTGT others(47): Show |
A | 9 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0152others(6): Show | 10 | HG01167.hp2 HG01192.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.402-1581_402-1528d others(56): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724985 | ||||||
| chr4:153724990
|
TGTGGGGG others(47): Show |
T | 58 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(55): Show | 78 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.402-1586_402-1533d others(56): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724990 | ||||||
| chr4:153725000
|
C | CGGGCAGG others(47): Show |
1 | a0003c0003t0001g0063 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.402-1543_402-1542i others(56): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725000 | ||||||
| chr4:153725024
|
G | A | 1 | a0004c0004t0001g0299 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.402-1566C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725024 | ||||||
| chr4:153725027
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.402-1569G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725027 | ||||||
| chr4:153725082
|
G | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0152others(4): Show | 8 | HG01167.hp2 HG01192.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.402-1624C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725082 | ||||||
| chr4:153725108
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.402-1650A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725108 | ||||||
| chr4:153725217
|
C | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0152others(6): Show | 10 | HG01167.hp2 HG01192.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.402-1759G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725217 | ||||||
| chr4:153725218
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(238): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.402-1760T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725218 | ||||||
| chr4:153725267
|
T | G | 51 | a0001c0001t0001g0228a0002c0002t0001g0004a0002c0002t0001g0005others(48): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.402-1809A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725267 | ||||||
| chr4:153725270
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0041others(7): Show | 15 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.402-1812C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725270 | ||||||
| chr4:153725307
|
T | G | 60 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0152others(57): Show | 80 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.402-1849A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725307 | ||||||
| chr4:153725523
|
T | C | 61 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0152others(58): Show | 81 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.402-2065A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725523 | ||||||
| chr4:153725600
|
G | T | 244 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(241): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.402-2142C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725600 | ||||||
| chr4:153725662
|
C | A | 2 | a0003c0003t0001g0070a0003c0003t0001g0071 | 2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.402-2204G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725662 | ||||||
| chr4:153725784
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0219 | 2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.402-2326A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725784 | ||||||
| chr4:153725842
|
A | G | 61 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0152others(58): Show | 81 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.401+2365T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725842 | ||||||
| chr4:153726073
|
A | ATGTG | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0154others(2): Show | 5 | HG01167.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.401+2130_401+2133d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726073 | ||||||
| chr4:153726073
|
A | ATGTGTG | 3 | a0001c0001t0001g0151a0001c0001t0001g0192a0001c0001t0001g0228 | 3 | HG01192.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.401+2128_401+2133d others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726073 | ||||||
| chr4:153726073
|
A | ATGTGTGT others(1): Show |
2 | a0001c0001t0001g0040a0003c0003t0001g0045 | 3 | HG02109.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.401+2126_401+2133d others(10): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726073 | ||||||
| chr4:153726073
|
ATG | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 167 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.401+2132_401+2133d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726073 | ||||||
| chr4:153726167
|
G | A | 1 | a0003c0003t0001g0074 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.401+2040C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726167 | ||||||
| chr4:153726229
|
C | T | 9 | a0001c0001t0001g0040a0001c0001t0001g0151a0001c0001t0001g0152others(6): Show | 10 | HG01167.hp2 HG01192.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.401+1978G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726229 | ||||||
| chr4:153726320
|
G | A | 1 | a0012c0014t0001g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.401+1887C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726320 | ||||||
| chr4:153726356
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.401+1851G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726356 | ||||||
| chr4:153726395
|
G | C | 1 | a0002c0002t0001g0161 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.401+1812C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726395 | ||||||
| chr4:153726470
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.401+1737A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726470 | ||||||
| chr4:153726476
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.401+1731A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726476 | ||||||
| chr4:153726479
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.401+1728A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726479 | ||||||
| chr4:153726484
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.401+1723C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726484 | ||||||
| chr4:153727000
|
C | T | 51 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(48): Show | 65 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.401+1207G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727000 | ||||||
| chr4:153727066
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.401+1141G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727066 | ||||||
| chr4:153727072
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0029a0001c0001t0001g0030others(22): Show | 36 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.401+1135G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727072 | ||||||
| chr4:153727129
|
T | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0198others(1): Show | 6 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.401+1078A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727129 | ||||||
| chr4:153727153
|
A | C | 1 | a0002c0002t0001g0161 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.401+1054T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727153 | ||||||
| chr4:153727652
|
C | T | 52 | a0001c0001t0001g0101a0001c0001t0001g0106a0001c0001t0001g0135others(49): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.401+555G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727652 | ||||||
| chr4:153727653
|
A | G | 148 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0016others(145): Show | 198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.401+554T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727653 | ||||||
| chr4:153728020
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0245 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.401+187A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153728020 | ||||||
| chr4:153728116
|
C | A | 1 | a0001c0001t0001g0177 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.401+91G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153728116 | ||||||
| chr4:153728657
|
T | G | 1 | a0001c0001t0001g0249 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.247-296A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153728657 | ||||||
| chr4:153728693
|
G | C | 1 | a0001c0001t0001g0303 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.247-332C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153728693 | ||||||
| chr4:153728954
|
T | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(104): Show | 134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.247-593A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153728954 | ||||||
| chr4:153729106
|
C | T | 2 | a0001c0001t0001g0249a0004c0004t0001g0233 | 2 | HG01358.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.247-745G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729106 | ||||||
| chr4:153729207
|
C | G | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-846G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729207 | ||||||
| chr4:153729277
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-916G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729277 | ||||||
| chr4:153729307
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-946G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729307 | ||||||
| chr4:153729308
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(151): Show | 210 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.247-947C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729308 | ||||||
| chr4:153729342
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(157): Show | 216 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.247-981G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729342 | ||||||
| chr4:153729386
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-1025C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729386 | ||||||
| chr4:153729544
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-1183C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729544 | ||||||
| chr4:153729667
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-1306C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729667 | ||||||
| chr4:153729735
|
A | G | 68 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(65): Show | 90 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.247-1374T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729735 | ||||||
| chr4:153729758
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.247-1397C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729758 | ||||||
| chr4:153729796
|
C | T | 154 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(151): Show | 210 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.247-1435G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729796 | ||||||
| chr4:153729899
|
C | CTCTT | 290 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 378 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.247-1539_247-1538i others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729899 | ||||||
| chr4:153730048
|
A | G | 2 | a0003c0003t0001g0055a0003c0003t0001g0059 | 2 | NA18972.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.247-1687T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730048 | ||||||
| chr4:153730202
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(169): Show | 230 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.247-1841A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730202 | ||||||
| chr4:153730297
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-1936C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730297 | ||||||
| chr4:153730403
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-2042G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730403 | ||||||
| chr4:153730444
|
G | A | 1 | a0002c0002t0001g0123 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.247-2083C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730444 | ||||||
| chr4:153730491
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-2130G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730491 | ||||||
| chr4:153730610
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-2249G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730610 | ||||||
| chr4:153730833
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-2472G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730833 | ||||||
| chr4:153730876
|
A | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-2515T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730876 | ||||||
| chr4:153730902
|
A | AAG | 1 | a0002c0002t0001g0014 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.247-2543_247-2542d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730902 | ||||||
| chr4:153731082
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-2721A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731082 | ||||||
| chr4:153731142
|
G | A | 292 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(289): Show | 380 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.247-2781C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731142 | ||||||
| chr4:153731177
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-2816T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731177 | ||||||
| chr4:153731295
|
A | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-2934T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731295 | ||||||
| chr4:153731409
|
C | T | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-3048G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731409 | ||||||
| chr4:153731496
|
T | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-3135A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731496 | ||||||
| chr4:153731529
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-3168G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731529 | ||||||
| chr4:153731665
|
A | AAGAG | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-3308_247-3305d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731665 | ||||||
| chr4:153731676
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-3315C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731676 | ||||||
| chr4:153731685
|
G | A | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-3324C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731685 | ||||||
| chr4:153731685
|
G | GAGGA | 67 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(64): Show | 89 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.247-3328_247-3325d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731685 | ||||||
| chr4:153731685
|
G | GAGGGAGG others(1): Show |
4 | a0002c0002t0001g0100a0002c0002t0001g0107a0002c0002t0001g0108others(1): Show | 4 | NA18944.hp1 NA18969.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-3325_247-3324i others(10): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731685 | ||||||
| chr4:153731929
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.247-3568C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731929 | ||||||
| chr4:153732104
|
C | T | 1 | a0001c0001t0003g0306 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.247-3743G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732104 | ||||||
| chr4:153732164
|
G | A | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(7): Show | 10 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-3803C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732164 | ||||||
| chr4:153732231
|
CA | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(155): Show | 214 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.247-3871delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732231 | ||||||
| chr4:153732238
|
A | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(104): Show | 134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.247-3877T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732238 | ||||||
| chr4:153732250
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.247-3889G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732250 | ||||||
| chr4:153732477
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-4116G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732477 | ||||||
| chr4:153732493
|
C | G | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.247-4132G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732493 | ||||||
| chr4:153732712
|
C | T | 16 | a0001c0001t0001g0193a0001c0001t0001g0217a0001c0001t0001g0293others(13): Show | 21 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.247-4351G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732712 | ||||||
| chr4:153732713
|
G | A | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-4352C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732713 | ||||||
| chr4:153732915
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-4554G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732915 | ||||||
| chr4:153732924
|
A | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(49): Show | 72 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.247-4563T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732924 | ||||||
| chr4:153732945
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-4584G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732945 | ||||||
| chr4:153732989
|
C | T | 1 | a0002c0002t0001g0140 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.247-4628G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732989 | ||||||
| chr4:153732993
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-4632G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732993 | ||||||
| chr4:153732998
|
G | A | 1 | a0001c0001t0001g0179 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.247-4637C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732998 | ||||||
| chr4:153733171
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 131 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.247-4810A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733171 | ||||||
| chr4:153733332
|
G | C | 3 | a0001c0001t0001g0234a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | HG02818.hp1 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247-4971C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733332 | ||||||
| chr4:153733491
|
A | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-5130T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733491 | ||||||
| chr4:153733513
|
G | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(81): Show | 118 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.247-5152C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733513 | ||||||
| chr4:153733612
|
G | A | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.247-5251C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733612 | ||||||
| chr4:153733813
|
CA | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-5453delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733813 | ||||||
| chr4:153733854
|
T | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0198a0001c0001t0001g0279others(7): Show | 11 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-5493A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733854 | ||||||
| chr4:153733889
|
CCACTGAT others(7): Show |
C | 1 | a0002c0002t0001g0139 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.247-5542_247-5529d others(16): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733889 | ||||||
| chr4:153734019
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-5658A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734019 | ||||||
| chr4:153734188
|
T | G | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-5827A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734188 | ||||||
| chr4:153734220
|
G | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-5859C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734220 | ||||||
| chr4:153734336
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.247-5975G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734336 | ||||||
| chr4:153734415
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.247-6054G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734415 | ||||||
| chr4:153734495
|
GAATT | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6138_247-6135d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734495 | ||||||
| chr4:153734571
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.247-6210G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734571 | ||||||
| chr4:153734665
|
C | CT | 9 | a0001c0001t0001g0152a0001c0001t0001g0213a0003c0003t0001g0011others(6): Show | 11 | HG01167.hp2 HG02135.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.247-6305dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | ||||||
| chr4:153734665
|
C | CTT | 10 | a0001c0001t0001g0033a0001c0001t0001g0150a0001c0001t0001g0151others(7): Show | 12 | HG01192.hp2 HG01884.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.247-6306_247-6305d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | ||||||
| chr4:153734665
|
CT | C | 38 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0083others(35): Show | 43 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.247-6305delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | ||||||
| chr4:153734665
|
CTT | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(104): Show | 146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.247-6306_247-6305d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | ||||||
| chr4:153734665
|
CTTT | C | 22 | a0001c0001t0001g0193a0001c0001t0001g0198a0001c0001t0001g0236others(19): Show | 27 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.247-6307_247-6305d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | ||||||
| chr4:153734665
|
CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0001g0106a0001c0001t0001g0135a0002c0002t0001g0013others(4): Show | 9 | NA18947.hp2 NA18952.hp2 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-6312_247-6305d others(10): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | ||||||
| chr4:153734665
|
CTTTTTTT others(2): Show |
C | 61 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(58): Show | 81 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.247-6313_247-6305d others(11): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | ||||||
| chr4:153734665
|
CTTTTTTT others(3): Show |
C | 2 | a0002c0002t0001g0086a0002c0002t0001g0093 | 2 | HG00597.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.247-6314_247-6305d others(12): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | ||||||
| chr4:153734665
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0235 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.247-6319_247-6305d others(17): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | ||||||
| chr4:153734670
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6309A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734670 | ||||||
| chr4:153734672
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6311A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734672 | ||||||
| chr4:153734674
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6313A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734674 | ||||||
| chr4:153734728
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01167.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.247-6367G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734728 | ||||||
| chr4:153734777
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 136 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.247-6416C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734777 | ||||||
| chr4:153734800
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0001g0259 | 2 | HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.247-6439G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734800 | ||||||
| chr4:153734801
|
G | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6440C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734801 | ||||||
| chr4:153734825
|
G | A | 1 | a0004c0004t0001g0291 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.247-6464C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734825 | ||||||
| chr4:153734860
|
T | G | 1 | a0011c0013t0001g0180 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.247-6499A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734860 | ||||||
| chr4:153734874
|
C | A | 93 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(90): Show | 117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.247-6513G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734874 | ||||||
| chr4:153734914
|
G | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6553C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734914 | ||||||
| chr4:153735006
|
A | G | 1 | a0002c0002t0001g0130 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.247-6645T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735006 | ||||||
| chr4:153735049
|
C | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(88): Show | 115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.247-6688G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735049 | ||||||
| chr4:153735108
|
T | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(185): Show | 251 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.247-6747A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735108 | ||||||
| chr4:153735227
|
A | ATTT | 14 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.247-6869_247-6867d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735227 | ||||||
| chr4:153735244
|
A | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6883T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735244 | ||||||
| chr4:153735258
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-6897A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735258 | ||||||
| chr4:153735347
|
G | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(46): Show | 66 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.247-6986C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735347 | ||||||
| chr4:153735384
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-7023A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735384 | ||||||
| chr4:153735523
|
C | T | 1 | a0012c0014t0001g0288 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.247-7162G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735523 | ||||||
| chr4:153735640
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-7279G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735640 | ||||||
| chr4:153735693
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-7332G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735693 | ||||||
| chr4:153735747
|
T | TA | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-7387_247-7386i others(3): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735747 | ||||||
| chr4:153735851
|
C | T | 1 | a0003c0003t0001g0055 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.247-7490G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735851 | ||||||
| chr4:153735886
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(153): Show | 212 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.247-7525A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735886 | ||||||
| chr4:153735955
|
A | T | 2 | a0003c0003t0001g0025a0003c0003t0001g0052 | 3 | NA18955.hp1 NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.247-7594T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735955 | ||||||
| chr4:153735999
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-7638G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735999 | ||||||
| chr4:153736208
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.247-7847G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736208 | ||||||
| chr4:153736251
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-7890A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736251 | ||||||
| chr4:153736427
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-8066G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736427 | ||||||
| chr4:153736455
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-8094A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736455 | ||||||
| chr4:153736630
|
A | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-8269T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736630 | ||||||
| chr4:153736710
|
C | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-8349G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736710 | ||||||
| chr4:153736722
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.247-8361G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736722 | ||||||
| chr4:153736728
|
C | T | 6 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(3): Show | 7 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-8367G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736728 | ||||||
| chr4:153736737
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-8376C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736737 | ||||||
| chr4:153736930
|
G | A | 1 | a0004c0004t0001g0225 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.247-8569C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736930 | ||||||
| chr4:153737050
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.247-8689C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737050 | ||||||
| chr4:153737083
|
A | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-8722T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737083 | ||||||
| chr4:153737112
|
G | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-8751C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737112 | ||||||
| chr4:153737160
|
A | G | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-8799T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737160 | ||||||
| chr4:153737187
|
T | C | 106 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(103): Show | 133 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.247-8826A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737187 | ||||||
| chr4:153737239
|
A | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-8878T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737239 | ||||||
| chr4:153737336
|
T | C | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-8975A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737336 | ||||||
| chr4:153737460
|
C | T | 2 | a0003c0003t0001g0045a0014c0009t0001g0046 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.247-9099G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737460 | ||||||
| chr4:153737550
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-9189A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737550 | ||||||
| chr4:153737772
|
CTGT | C | 70 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(67): Show | 92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.247-9414_247-9412d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737772 | ||||||
| chr4:153737876
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(168): Show | 232 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.247-9515G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737876 | ||||||
| chr4:153738086
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-9725C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738086 | ||||||
| chr4:153738122
|
T | C | 1 | a0002c0002t0001g0126 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.247-9761A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738122 | ||||||
| chr4:153738287
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.247-9926G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738287 | ||||||
| chr4:153738344
|
T | C | 1 | a0003c0003t0001g0078 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.247-9983A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738344 | ||||||
| chr4:153738350
|
A | AT | 88 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(85): Show | 115 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.247-9990dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738350 | ||||||
| chr4:153738376
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(177): Show | 243 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.247-10015T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738376 | ||||||
| chr4:153738408
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.247-10047C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738408 | ||||||
| chr4:153738751
|
T | C | 1 | a0002c0002t0001g0127 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+9894A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738751 | ||||||
| chr4:153738820
|
G | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+9825C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738820 | ||||||
| chr4:153738828
|
C | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+9817G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738828 | ||||||
| chr4:153738980
|
T | C | 6 | a0001c0001t0001g0141a0002c0002t0001g0006a0002c0002t0001g0128others(3): Show | 9 | HG00423.hp2 HG02165.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+9665A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738980 | ||||||
| chr4:153738997
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.246+9648G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738997 | ||||||
| chr4:153739077
|
A | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(170): Show | 231 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.246+9568T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739077 | ||||||
| chr4:153739227
|
C | T | 2 | a0003c0003t0001g0045a0014c0009t0001g0046 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.246+9418G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739227 | ||||||
| chr4:153739313
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+9332G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739313 | ||||||
| chr4:153739487
|
T | G | 2 | a0003c0003t0001g0045a0014c0009t0001g0046 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.246+9158A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739487 | ||||||
| chr4:153739660
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+8985T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739660 | ||||||
| chr4:153739722
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+8923G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739722 | ||||||
| chr4:153739792
|
C | T | 4 | a0001c0001t0001g0018a0001c0001t0001g0211a0001c0001t0001g0259others(1): Show | 6 | HG00733.hp2 HG01109.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+8853G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739792 | ||||||
| chr4:153739796
|
G | A | 4 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0247others(1): Show | 4 | HG02976.hp2 HG03471.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+8849C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739796 | ||||||
| chr4:153739813
|
C | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0244 | 2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.246+8832G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739813 | ||||||
| chr4:153740059
|
AT | A | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+8585delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740059 | ||||||
| chr4:153740122
|
A | G | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+8523T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740122 | ||||||
| chr4:153740166
|
A | AT | 70 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(67): Show | 92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.246+8478dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740166 | ||||||
| chr4:153740166
|
AT | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+8478delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740166 | ||||||
| chr4:153740534
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 220 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.246+8111A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740534 | ||||||
| chr4:153740603
|
C | A | 70 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(67): Show | 92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.246+8042G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740603 | ||||||
| chr4:153740623
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+8022A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740623 | ||||||
| chr4:153740815
|
A | G | 1 | a0007c0007t0001g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.246+7830T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740815 | ||||||
| chr4:153740923
|
C | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.246+7722G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740923 | ||||||
| chr4:153741045
|
C | T | 1 | a0001c0001t0001g0257 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.246+7600G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741045 | ||||||
| chr4:153741075
|
C | T | 20 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(17): Show | 25 | HG00099.hp1 HG00323.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.246+7570G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741075 | ||||||
| chr4:153741171
|
GT | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(39): Show | 60 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.246+7473delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741171 | ||||||
| chr4:153741246
|
G | T | 2 | a0001c0001t0001g0273a0010c0012t0001g0255 | 2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.246+7399C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741246 | ||||||
| chr4:153741279
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(168): Show | 232 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.246+7366A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741279 | ||||||
| chr4:153741310
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.246+7335G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741310 | ||||||
| chr4:153741312
|
G | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+7333C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741312 | ||||||
| chr4:153741319
|
C | T | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+7326G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741319 | ||||||
| chr4:153741451
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+7194G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741451 | ||||||
| chr4:153741463
|
T | C | 1 | a0003c0003t0001g0075 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.246+7182A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741463 | ||||||
| chr4:153741517
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.246+7128A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741517 | ||||||
| chr4:153741557
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.246+7088G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741557 | ||||||
| chr4:153741741
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0134 | 2 | NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.246+6904A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741741 | ||||||
| chr4:153742131
|
A | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+6514T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742131 | ||||||
| chr4:153742142
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.246+6503G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742142 | ||||||
| chr4:153742272
|
C | CA | 95 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(92): Show | 120 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.246+6372dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742272 | ||||||
| chr4:153742272
|
C | CAA | 115 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0084others(112): Show | 152 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.246+6371_246+6372d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742272 | ||||||
| chr4:153742272
|
C | CAAA | 57 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(54): Show | 78 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.246+6370_246+6372d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742272 | ||||||
| chr4:153742325
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+6320C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742325 | ||||||
| chr4:153742739
|
C | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(168): Show | 232 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.246+5906G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742739 | ||||||
| chr4:153742803
|
A | G | 41 | a0001c0001t0001g0098a0001c0001t0001g0136a0003c0003t0001g0002others(38): Show | 57 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.246+5842T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742803 | ||||||
| chr4:153742913
|
A | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.246+5732T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742913 | ||||||
| chr4:153742974
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.246+5671T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742974 | ||||||
| chr4:153743109
|
C | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+5536G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743109 | ||||||
| chr4:153743143
|
G | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+5502C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743143 | ||||||
| chr4:153743240
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.246+5405T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743240 | ||||||
| chr4:153743310
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0272 | 5 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+5335T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743310 | ||||||
| chr4:153743352
|
C | T | 2 | a0003c0003t0001g0045a0014c0009t0001g0046 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.246+5293G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743352 | ||||||
| chr4:153743371
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(98): Show | 137 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+5274T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743371 | ||||||
| chr4:153743417
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(185): Show | 251 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.246+5228C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743417 | ||||||
| chr4:153743545
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.246+5100A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743545 | ||||||
| chr4:153743545
|
T | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(169): Show | 230 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.246+5100A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743545 | ||||||
| chr4:153743556
|
T | G | 1 | a0001c0001t0001g0135 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.246+5089A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743556 | ||||||
| chr4:153743636
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 250 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.246+5009C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743636 | ||||||
| chr4:153743640
|
G | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+5005C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743640 | ||||||
| chr4:153743642
|
T | C | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+5003A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743642 | ||||||
| chr4:153743773
|
G | T | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+4872C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743773 | ||||||
| chr4:153743869
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(185): Show | 251 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.246+4776A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743869 | ||||||
| chr4:153744051
|
C | A | 1 | a0003c0003t0001g0023 | 2 | HG00733.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.246+4594G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744051 | ||||||
| chr4:153744061
|
C | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(186): Show | 252 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.246+4584G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744061 | ||||||
| chr4:153744076
|
G | C | 1 | a0001c0001t0001g0031 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.246+4569C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744076 | ||||||
| chr4:153744127
|
A | G | 70 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(67): Show | 92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.246+4518T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744127 | ||||||
| chr4:153744147
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0216 | 2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.246+4498G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744147 | ||||||
| chr4:153744278
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.246+4367G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744278 | ||||||
| chr4:153744283
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+4362C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744283 | ||||||
| chr4:153744295
|
G | A | 36 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0035others(33): Show | 42 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.246+4350C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744295 | ||||||
| chr4:153744426
|
G | GA | 5 | a0001c0001t0001g0007a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 8 | NA18945.hp2 NA18955.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+4218dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744426 | ||||||
| chr4:153744426
|
GA | G | 14 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(11): Show | 15 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.246+4218delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744426 | ||||||
| chr4:153744548
|
A | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+4097T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744548 | ||||||
| chr4:153744581
|
C | A | 68 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(65): Show | 90 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.246+4064G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744581 | ||||||
| chr4:153744747
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.246+3898G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744747 | ||||||
| chr4:153744826
|
A | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+3819T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744826 | ||||||
| chr4:153744852
|
C | T | 1 | a0002c0002t0001g0163 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.246+3793G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744852 | ||||||
| chr4:153744908
|
C | T | 1 | a0003c0003t0001g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.246+3737G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744908 | ||||||
| chr4:153745046
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.246+3599T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745046 | ||||||
| chr4:153745094
|
A | G | 15 | a0001c0001t0001g0033a0001c0001t0001g0150a0001c0001t0001g0151others(12): Show | 16 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.246+3551T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745094 | ||||||
| chr4:153745169
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+3476A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745169 | ||||||
| chr4:153745695
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.246+2950A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745695 | ||||||
| chr4:153745747
|
A | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+2898T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745747 | ||||||
| chr4:153745965
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.246+2680G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745965 | ||||||
| chr4:153746230
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(167): Show | 231 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.246+2415C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746230 | ||||||
| chr4:153746294
|
A | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+2351T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746294 | ||||||
| chr4:153746295
|
C | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+2350G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746295 | ||||||
| chr4:153746432
|
T | TCCATAGC others(30): Show |
1 | a0001c0001t0001g0184 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.246+2212_246+2213i others(39): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746432 | ||||||
| chr4:153746432
|
TCCGTAGC others(30): Show |
T | 1 | a0002c0002t0001g0162 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.246+2176_246+2212d others(39): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746432 | ||||||
| chr4:153746435
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(166): Show | 230 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.246+2210C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746435 | ||||||
| chr4:153746556
|
TAGGCTGG others(30): Show |
T | 1 | a0002c0002t0001g0162 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.246+2052_246+2088d others(39): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746556 | ||||||
| chr4:153746617
|
C | A | 1 | a0004c0004t0001g0297 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.246+2028G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746617 | ||||||
| chr4:153746689
|
C | T | 3 | a0001c0001t0001g0193a0003c0003t0001g0045a0014c0009t0001g0046 | 3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.246+1956G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746689 | ||||||
| chr4:153746878
|
C | T | 2 | a0001c0001t0001g0273a0010c0012t0001g0255 | 2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.246+1767G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746878 | ||||||
| chr4:153746883
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+1762T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746883 | ||||||
| chr4:153746891
|
C | T | 2 | a0003c0003t0001g0045a0009c0011t0001g0230 | 2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.246+1754G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746891 | ||||||
| chr4:153746900
|
C | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+1745G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746900 | ||||||
| chr4:153746951
|
C | T | 2 | a0001c0001t0001g0273a0010c0012t0001g0255 | 2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.246+1694G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746951 | ||||||
| chr4:153747076
|
C | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+1569G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747076 | ||||||
| chr4:153747095
|
G | A | 1 | a0003c0003t0001g0075 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.246+1550C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747095 | ||||||
| chr4:153747126
|
C | A | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+1519G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747126 | ||||||
| chr4:153747183
|
A | G | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+1462T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747183 | ||||||
| chr4:153747221
|
G | A | 1 | a0004c0004t0001g0298 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.246+1424C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747221 | ||||||
| chr4:153747258
|
G | C | 1 | a0003c0003t0001g0076 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.246+1387C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747258 | ||||||
| chr4:153747277
|
T | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(104): Show | 134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.246+1368A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747277 | ||||||
| chr4:153747455
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+1190C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747455 | ||||||
| chr4:153747522
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.246+1123A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747522 | ||||||
| chr4:153747614
|
C | T | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(7): Show | 10 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+1031G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747614 | ||||||
| chr4:153747812
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.246+833C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747812 | ||||||
| chr4:153748020
|
C | T | 1 | a0003c0003t0001g0078 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.246+625G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748020 | ||||||
| chr4:153748193
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+452T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748193 | ||||||
| chr4:153748319
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 211 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.246+326G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748319 | ||||||
| chr4:153748446
|
C | G | 1 | a0007c0007t0001g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.246+199G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748446 | ||||||
| chr4:153748446
|
C | T | 2 | a0003c0003t0001g0024a0013c0010t0001g0050 | 3 | HG01081.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.246+199G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748446 | ||||||
| chr4:153748581
|
G | A | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+64C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748581 | ||||||
| chr4:153748793
|
C | T | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(7): Show | 10 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.105-7G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153748793 | ||||||
| chr4:153748841
|
C | CAAAA | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.105-59_105-56dupTT others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153748841 | ||||||
| chr4:153748849
|
A | C | 2 | a0001c0001t0001g0253a0001c0001t0001g0254 | 2 | HG02004.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.105-63T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153748849 | ||||||
| chr4:153749002
|
T | C | 1 | a0007c0007t0001g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.105-216A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749002 | ||||||
| chr4:153749104
|
G | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(168): Show | 232 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.105-318C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749104 | ||||||
| chr4:153749292
|
T | C | 70 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(67): Show | 92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.105-506A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749292 | ||||||
| chr4:153749381
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.105-595A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749381 | ||||||
| chr4:153749424
|
A | T | 2 | a0003c0003t0001g0045a0014c0009t0001g0046 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.105-638T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749424 | ||||||
| chr4:153749506
|
G | A | 1 | a0007c0007t0001g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.105-720C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749506 | ||||||
| chr4:153749607
|
G | A | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | NA19000.hp1 NA19083.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.105-821C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749607 | ||||||
| chr4:153749646
|
T | C | 70 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(67): Show | 92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.105-860A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749646 | ||||||
| chr4:153749661
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(89): Show | 126 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.105-875T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749661 | ||||||
| chr4:153749929
|
T | C | 1 | a0001c0001t0001g0031 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.105-1143A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749929 | ||||||
| chr4:153750244
|
A | G | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.104+1194T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750244 | ||||||
| chr4:153750274
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.104+1164C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750274 | ||||||
| chr4:153750303
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.104+1135T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750303 | ||||||
| chr4:153750316
|
T | A | 69 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(66): Show | 91 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.104+1122A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750316 | ||||||
| chr4:153750323
|
C | G | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.104+1115G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750323 | ||||||
| chr4:153750324
|
T | C | 15 | a0001c0001t0001g0193a0001c0001t0001g0293a0004c0004t0001g0010others(12): Show | 20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.104+1114A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750324 | ||||||
| chr4:153750657
|
T | TAAACAAA others(1): Show |
113 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(110): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.104+773_104+780dup others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750657 | ||||||
| chr4:153750667
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0029others(37): Show | 55 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.104+771T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750667 | ||||||
| chr4:153750668
|
G | A | 15 | a0001c0001t0001g0033a0001c0001t0001g0150a0001c0001t0001g0151others(12): Show | 16 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.104+770C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750668 | ||||||
| chr4:153750669
|
C | CAAACAAG others(2): Show |
15 | a0001c0001t0001g0033a0001c0001t0001g0150a0001c0001t0001g0151others(12): Show | 16 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.104+768_104+769ins others(9): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750669 | ||||||
| chr4:153750836
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104+602T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750836 | ||||||
| chr4:153750876
|
CTTTATGA others(19): Show |
C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | NA18954.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.104+536_104+561del others(26): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750876 | ||||||
| chr4:153750878
|
T | TTATGAGA others(19): Show |
14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.104+534_104+559dup others(26): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750878 | ||||||
| chr4:153750892
|
T | TATTAATC others(19): Show |
1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104+545_104+546ins others(26): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750892 | ||||||
| chr4:153750981
|
G | T | 6 | a0002c0002t0001g0005a0002c0002t0001g0012a0002c0002t0001g0082others(3): Show | 12 | HG00558.hp2 HG01433.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.104+457C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750981 | ||||||
| chr4:153751553
|
A | G | 1 | a0002c0002t0001g0162 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.67-78T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153751553 | ||||||
| chr4:153751695
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.67-220A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153751695 | ||||||
| chr4:153751893
|
G | C | 1 | a0001c0001t0001g0272 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.67-418C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153751893 | ||||||
| chr4:153751975
|
T | C | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.67-500A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153751975 | ||||||
| chr4:153752173
|
G | T | 1 | a0002c0002t0001g0094 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.67-698C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752173 | ||||||
| chr4:153752517
|
T | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(104): Show | 134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.67-1042A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752517 | ||||||
| chr4:153752598
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.67-1123A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752598 | ||||||
| chr4:153752694
|
T | C | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.67-1219A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752694 | ||||||
| chr4:153752770
|
G | A | 4 | a0002c0002t0001g0006a0002c0002t0001g0137a0002c0002t0001g0138others(1): Show | 7 | HG00423.hp2 HG02165.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-1295C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752770 | ||||||
| chr4:153752853
|
G | A | 1 | a0004c0004t0001g0299 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.67-1378C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752853 | ||||||
| chr4:153752880
|
A | G | 4 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(1): Show | 4 | NA18948.hp1 NA18971.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-1405T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752880 | ||||||
| chr4:153752928
|
G | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(79): Show | 116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-1453C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752928 | ||||||
| chr4:153752943
|
G | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.67-1468C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752943 | ||||||
| chr4:153752968
|
C | T | 1 | a0002c0002t0001g0161 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.67-1493G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752968 | ||||||
| chr4:153752994
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.67-1519G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752994 | ||||||
| chr4:153753040
|
T | A | 57 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(54): Show | 75 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.67-1565A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753040 | ||||||
| chr4:153753048
|
C | T | 117 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(114): Show | 144 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.67-1573G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753048 | ||||||
| chr4:153753058
|
G | A | 1 | a0003c0003t0001g0076 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.67-1583C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753058 | ||||||
| chr4:153753071
|
G | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-1596C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753071 | ||||||
| chr4:153753072
|
A | T | 4 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-1597T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753072 | ||||||
| chr4:153753126
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(179): Show | 243 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.67-1651G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753126 | ||||||
| chr4:153753227
|
G | A | 1 | a0002c0002t0001g0140 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67-1752C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753227 | ||||||
| chr4:153753335
|
GGCT | G | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(7): Show | 10 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-1863_67-1861del others(3): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753335 | ||||||
| chr4:153753339
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.67-1864T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753339 | ||||||
| chr4:153753449
|
C | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(104): Show | 134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.67-1974G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753449 | ||||||
| chr4:153753542
|
TTC | T | 92 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(89): Show | 119 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.67-2069_67-2068del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753542 | ||||||
| chr4:153753542
|
TTCTC | T | 3 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0093 | 3 | HG01099.hp2 HG01109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.67-2071_67-2068del others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753542 | ||||||
| chr4:153753558
|
CTCT | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 129 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.67-2086_67-2084del others(3): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753558 | ||||||
| chr4:153753575
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.67-2100C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753575 | ||||||
| chr4:153753596
|
C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(175): Show | 234 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.67-2121G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753596 | ||||||
| chr4:153753690
|
T | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.67-2215A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753690 | ||||||
| chr4:153753719
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(298): Show | 389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.67-2244T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753719 | ||||||
| chr4:153753838
|
C | T | 2 | a0003c0003t0001g0048a0003c0003t0001g0049 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.67-2363G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753838 | ||||||
| chr4:153753896
|
C | T | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-2421G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753896 | ||||||
| chr4:153753903
|
G | A | 2 | a0003c0003t0001g0045a0014c0009t0001g0046 | 2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.67-2428C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753903 | ||||||
| chr4:153753941
|
C | T | 1 | a0004c0004t0001g0291 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.67-2466G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753941 | ||||||
| chr4:153753947
|
T | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.67-2472A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753947 | ||||||
| chr4:153753953
|
G | A | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.67-2478C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753953 | ||||||
| chr4:153753966
|
A | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.67-2491T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753966 | ||||||
| chr4:153753986
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.67-2511A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753986 | ||||||
| chr4:153754031
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(211): Show | 275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.67-2556C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754031 | ||||||
| chr4:153754072
|
C | T | 7 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 7 | HG00642.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2597G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754072 | ||||||
| chr4:153754095
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(211): Show | 275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.67-2620C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754095 | ||||||
| chr4:153754131
|
CT | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(212): Show | 276 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.67-2657delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754131 | ||||||
| chr4:153754169
|
C | CA | 80 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(77): Show | 103 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.67-2695dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754169 | ||||||
| chr4:153754181
|
A | AG | 211 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(208): Show | 272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.67-2707_67-2706ins others(1): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754181 | ||||||
| chr4:153754181
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.67-2706T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754181 | ||||||
| chr4:153754261
|
G | T | 3 | a0001c0001t0001g0193a0003c0003t0001g0045a0014c0009t0001g0046 | 3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67-2786C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754261 | ||||||
| chr4:153754490
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.67-3015A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754490 | ||||||
| chr4:153754508
|
A | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3033T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754508 | ||||||
| chr4:153754511
|
C | T | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3036G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754511 | ||||||
| chr4:153754514
|
G | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3039C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754514 | ||||||
| chr4:153754515
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3040C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754515 | ||||||
| chr4:153754516
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3041A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754516 | ||||||
| chr4:153754517
|
T | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3042A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754517 | ||||||
| chr4:153754518
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3043A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754518 | ||||||
| chr4:153754520
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3045C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754520 | ||||||
| chr4:153754521
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3046C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754521 | ||||||
| chr4:153754524
|
C | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3049G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754524 | ||||||
| chr4:153754527
|
T | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3052A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754527 | ||||||
| chr4:153754530
|
T | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3055A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754530 | ||||||
| chr4:153754531
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3056C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754531 | ||||||
| chr4:153754532
|
A | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3057T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754532 | ||||||
| chr4:153754534
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3059A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754534 | ||||||
| chr4:153754535
|
T | G | 2 | a0001c0001t0001g0193a0005c0005t0001g0202 | 2 | HG04228.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.67-3060A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754535 | ||||||
| chr4:153754539
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3064A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754539 | ||||||
| chr4:153754540
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3065A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754540 | ||||||
| chr4:153754542
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3067A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754542 | ||||||
| chr4:153754553
|
A | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3078T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754553 | ||||||
| chr4:153754558
|
A | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3083T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754558 | ||||||
| chr4:153754560
|
G | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3085C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754560 | ||||||
| chr4:153754562
|
T | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3087A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754562 | ||||||
| chr4:153754564
|
G | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3089C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754564 | ||||||
| chr4:153754566
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3091C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754566 | ||||||
| chr4:153754567
|
T | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3092A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754567 | ||||||
| chr4:153754568
|
C | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3093G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754568 | ||||||
| chr4:153754569
|
C | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3094G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754569 | ||||||
| chr4:153754570
|
T | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3095A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754570 | ||||||
| chr4:153754574
|
C | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3099G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754574 | ||||||
| chr4:153754576
|
C | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3101G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754576 | ||||||
| chr4:153754577
|
C | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3102G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754577 | ||||||
| chr4:153754580
|
T | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3105A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754580 | ||||||
| chr4:153754582
|
C | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3107G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754582 | ||||||
| chr4:153754583
|
C | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3108G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754583 | ||||||
| chr4:153754584
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3109A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754584 | ||||||
| chr4:153754586
|
T | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3111A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754586 | ||||||
| chr4:153754587
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3112C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754587 | ||||||
| chr4:153754590
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3115A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754590 | ||||||
| chr4:153754592
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3117A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754592 | ||||||
| chr4:153754598
|
T | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3123A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754598 | ||||||
| chr4:153754600
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3125A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754600 | ||||||
| chr4:153754603
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3128C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754603 | ||||||
| chr4:153754604
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3129C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754604 | ||||||
| chr4:153754608
|
T | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3133A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754608 | ||||||
| chr4:153754610
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3135C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754610 | ||||||
| chr4:153754610
|
G | C | 1 | a0001c0001t0001g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67-3135C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754610 | ||||||
| chr4:153754611
|
G | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3136C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754611 | ||||||
| chr4:153754613
|
T | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3138A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754613 | ||||||
| chr4:153754619
|
C | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3144G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754619 | ||||||
| chr4:153754622
|
A | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3147T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754622 | ||||||
| chr4:153754623
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3148A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754623 | ||||||
| chr4:153754625
|
T | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3150A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754625 | ||||||
| chr4:153754628
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3153A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754628 | ||||||
| chr4:153754629
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3154A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754629 | ||||||
| chr4:153754635
|
C | T | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3160G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754635 | ||||||
| chr4:153754639
|
A | T | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3164T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754639 | ||||||
| chr4:153754640
|
G | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3165C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754640 | ||||||
| chr4:153754643
|
T | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3168A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754643 | ||||||
| chr4:153754646
|
G | C | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3171C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754646 | ||||||
| chr4:153754648
|
C | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3173G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754648 | ||||||
| chr4:153754651
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3176A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754651 | ||||||
| chr4:153754662
|
G | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3187C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754662 | ||||||
| chr4:153754664
|
C | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3189G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754664 | ||||||
| chr4:153754668
|
T | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3193A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754668 | ||||||
| chr4:153754669
|
C | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3194G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754669 | ||||||
| chr4:153754670
|
C | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3195G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754670 | ||||||
| chr4:153754671
|
T | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3196A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754671 | ||||||
| chr4:153754673
|
A | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3198T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754673 | ||||||
| chr4:153754675
|
T | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3200A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754675 | ||||||
| chr4:153754676
|
C | A | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3201G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754676 | ||||||
| chr4:153754677
|
C | G | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3202G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754677 | ||||||
| chr4:153754679
|
A | T | 1 | a0005c0005t0001g0202 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3204T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754679 | ||||||
| chr4:153754708
|
C | T | 117 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(114): Show | 144 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.67-3233G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754708 | ||||||
| chr4:153754765
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.67-3290C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754765 | ||||||
| chr4:153754788
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.67-3313T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754788 | ||||||
| chr4:153754938
|
AT | A | 10 | a0001c0001t0001g0041a0001c0001t0001g0198a0001c0001t0001g0279others(7): Show | 11 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.67-3464delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754938 | ||||||
| chr4:153754957
|
G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(211): Show | 275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.67-3482C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754957 | ||||||
| chr4:153755055
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-3580C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755055 | ||||||
| chr4:153755289
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.67-3814T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755289 | ||||||
| chr4:153755403
|
A | G | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01496.hp2 HG02698.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-3928T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755403 | ||||||
| chr4:153755563
|
C | G | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01496.hp2 HG02698.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-4088G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755563 | ||||||
| chr4:153755574
|
T | TA | 123 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(120): Show | 150 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.67-4100dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755574 | ||||||
| chr4:153755668
|
G | C | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.66+4129C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755668 | ||||||
| chr4:153755669
|
C | A | 1 | a0002c0002t0001g0142 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.66+4128G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755669 | ||||||
| chr4:153755669
|
C | CA | 82 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(79): Show | 109 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.66+4127dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755669 | ||||||
| chr4:153755670
|
A | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(211): Show | 275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.66+4127T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755670 | ||||||
| chr4:153755802
|
C | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0219 | 3 | HG03041.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.66+3995G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755802 | ||||||
| chr4:153755803
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.66+3994C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755803 | ||||||
| chr4:153755822
|
T | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 13 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.66+3975A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755822 | ||||||
| chr4:153756271
|
A | C | 125 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(122): Show | 152 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.66+3526T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756271 | ||||||
| chr4:153756297
|
C | T | 2 | a0002c0002t0001g0155a0002c0002t0001g0156 | 2 | HG00280.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.66+3500G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756297 | ||||||
| chr4:153756391
|
A | G | 23 | a0001c0001t0001g0033a0001c0001t0001g0150a0001c0001t0001g0151others(20): Show | 24 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.66+3406T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756391 | ||||||
| chr4:153756413
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(211): Show | 275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.66+3384A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756413 | ||||||
| chr4:153756458
|
T | C | 85 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0085others(82): Show | 112 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.66+3339A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756458 | ||||||
| chr4:153756482
|
G | C | 126 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(123): Show | 153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.66+3315C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756482 | ||||||
| chr4:153756516
|
C | T | 8 | a0001c0001t0001g0201a0001c0001t0001g0204a0005c0005t0001g0202others(5): Show | 8 | HG02615.hp1 HG03130.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+3281G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756516 | ||||||
| chr4:153756704
|
G | T | 125 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(122): Show | 152 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.66+3093C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756704 | ||||||
| chr4:153756936
|
C | A | 1 | a0006c0006t0001g0300 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.66+2861G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756936 | ||||||
| chr4:153756989
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.66+2808G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756989 | ||||||
| chr4:153757051
|
A | G | 7 | a0001c0001t0001g0033a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 8 | HG02451.hp1 HG02486.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+2746T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757051 | ||||||
| chr4:153757084
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.66+2713T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757084 | ||||||
| chr4:153757115
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.66+2682G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757115 | ||||||
| chr4:153757160
|
G | T | 1 | a0001c0001t0001g0085 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.66+2637C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757160 | ||||||
| chr4:153757211
|
A | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(211): Show | 275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.66+2586T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757211 | ||||||
| chr4:153757471
|
A | G | 299 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(296): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.66+2326T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757471 | ||||||
| chr4:153757583
|
C | T | 1 | a0002c0002t0001g0082 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.66+2214G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757583 | ||||||
| chr4:153757747
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.66+2050G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757747 | ||||||
| chr4:153758179
|
A | G | 71 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0083others(68): Show | 93 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.66+1618T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758179 | ||||||
| chr4:153758320
|
G | C | 1 | a0005c0005t0001g0210 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.66+1477C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758320 | ||||||
| chr4:153758550
|
G | A | 12 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(9): Show | 12 | HG02615.hp1 HG03130.hp2 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+1247C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758550 | ||||||
| chr4:153758615
|
G | A | 14 | a0001c0001t0001g0293a0004c0004t0001g0010a0004c0004t0001g0043others(11): Show | 19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+1182C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758615 | ||||||
| chr4:153758674
|
C | A | 4 | a0003c0003t0001g0011a0003c0003t0001g0026a0003c0003t0001g0080others(1): Show | 7 | HG02135.hp2 NA18942.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+1123G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758674 | ||||||
| chr4:153758713
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(215): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.66+1084A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758713 | ||||||
| chr4:153758797
|
C | T | 1 | a0003c0003t0001g0023 | 2 | HG00733.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.66+1000G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758797 | ||||||
| chr4:153758829
|
T | A | 175 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(172): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.66+968A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758829 | ||||||
| chr4:153758855
|
T | C | 175 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(172): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.66+942A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758855 | ||||||
| chr4:153758894
|
G | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(51): Show | 72 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.66+903C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758894 | ||||||
| chr4:153759056
|
C | T | 6 | a0001c0001t0001g0195a0001c0001t0001g0198a0005c0005t0001g0032others(3): Show | 7 | HG02572.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+741G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153759056 | ||||||
| chr4:153759117
|
T | G | 175 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(172): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.66+680A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153759117 | ||||||
| chr4:153759344
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0301a0001c0001t0001g0302others(3): Show | 8 | HG01346.hp1 HG01358.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+453C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153759344 |