Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 27333 |
|---|---|
| ensemblid | ENSG00000173905.9 |
| hgncid | 15448 |
| symbol | GOLIM4 |
| name | golgi integral membrane protein 4 |
| refseq_nuc | NM_014498.5 |
| refseq_prot | NP_055313.1 |
| ensembl_nuc | ENST00000470487.6 |
| ensembl_prot | ENSP00000417354.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 168008689 |
| end | 168095924 |
| strand | - |
| ver | v1.2 |
| region | chr3:168008689-168095924 |
| region5000 | chr3:168003689-168100924 |
| regionname0 | GOLIM4_chr3_168008689_168095924 |
| regionname5000 | GOLIM4_chr3_168003689_168100924 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 696 | 189 | 60 | 49 | 36 | 14 | 28 | 30 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002 | 0/0 | 696 | 21 | 20 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0003 | 0/0 | 696 | 8 | 0 | 0 | 6 | 0 | 2 | 4 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0004 | 0/0 | 696 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0005 | 0/0 | 696 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0006 | 0/0 | 696 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2091 | 183 | 59 | 46 | 35 | 13 | 28 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| c0002 | 0/0 | 2091 | 21 | 20 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| c0003 | 0/0 | 2091 | 8 | 0 | 0 | 6 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| c0004 | 0/0 | 2091 | 6 | 6 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| c0005 | 0/0 | 2091 | 3 | 0 | 3 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| c0006 | 0/0 | 2091 | 3 | 0 | 1 | 2 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| c0007 | 0/0 | 2091 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| c0008 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| c0009 | 0/0 | 2091 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| c0010 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2234 | 49 | 6 | 14 | 16 | 5 | 8 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0002 | 0/0 | 2223 | 22 | 17 | 2 | 1 | 1 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0003 | 0/1 | 2234 | 20 | 1 | 7 | 4 | 0 | 7 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0004 | 0/0 | 2231 | 20 | 0 | 9 | 3 | 5 | 3 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0005 | 0/0 | 2226 | 14 | 11 | 0 | 1 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0006 | 0/0 | 2223 | 10 | 0 | 4 | 6 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0007 | 0/0 | 2223 | 9 | 8 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0008 | 0/0 | 2224 | 9 | 6 | 1 | 2 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0009 | 0/0 | 2233 | 7 | 0 | 2 | 2 | 1 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0010 | 0/0 | 2235 | 6 | 0 | 2 | 1 | 2 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0011 | 0/0 | 2235 | 6 | 2 | 2 | 0 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0012 | 0/0 | 2223 | 5 | 5 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0013 | 0/0 | 2227 | 5 | 0 | 1 | 4 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0014 | 0/0 | 2226 | 4 | 3 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0015 | 0/0 | 2232 | 4 | 0 | 2 | 0 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0016 | 0/0 | 2224 | 3 | 3 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0017 | 0/0 | 2225 | 3 | 2 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0018 | 0/0 | 2224 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0019 | 0/0 | 2224 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0020 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0021 | 0/0 | 2223 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0022 | 0/0 | 2224 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0023 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0024 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0025 | 0/0 | 2227 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0026 | 0/0 | 2220 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0027 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0028 | 0/0 | 2236 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0029 | 1/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0030 | 0/0 | 2227 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0031 | 0/0 | 2230 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0032 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0033 | 0/0 | 2234 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0034 | 0/0 | 2231 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0035 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0036 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0037 | 0/0 | 2223 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0038 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0039 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0040 | 0/0 | 2224 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0041 | 0/0 | 2223 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0042 | 0/0 | 2234 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0043 | 0/0 | 2235 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| t0044 | 0/0 | 2234 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2091 | 183 | 59 | 46 | 35 | 13 | 28 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0005 | 0/0 | 2091 | 3 | 0 | 3 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0008 | 0/0 | 2091 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0009 | 0/0 | 2091 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0010 | 0/0 | 2091 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002 | 0/0 | 2091 | 21 | 20 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0003c0003 | 0/0 | 2091 | 8 | 0 | 0 | 6 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0004c0004 | 0/0 | 2091 | 6 | 6 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0005c0006 | 0/0 | 2091 | 3 | 0 | 1 | 2 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0006c0007 | 0/0 | 2091 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4324 | 44 | 5 | 11 | 15 | 5 | 8 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0002 | 0/0 | 4313 | 15 | 11 | 1 | 1 | 1 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0003 | 0/1 | 4324 | 20 | 1 | 7 | 4 | 0 | 7 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0004 | 0/0 | 4321 | 19 | 0 | 9 | 3 | 4 | 3 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0005 | 0/0 | 4316 | 3 | 3 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0006 | 0/0 | 4313 | 10 | 0 | 4 | 6 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0007 | 0/0 | 4313 | 8 | 7 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0008 | 0/0 | 4314 | 5 | 5 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0009 | 0/0 | 4323 | 7 | 0 | 2 | 2 | 1 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0010 | 0/0 | 4325 | 6 | 0 | 2 | 1 | 2 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0011 | 0/0 | 4325 | 5 | 1 | 2 | 0 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0012 | 0/0 | 4313 | 5 | 5 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0014 | 0/0 | 4316 | 4 | 3 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0015 | 0/0 | 4322 | 4 | 0 | 2 | 0 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0016 | 0/0 | 4314 | 3 | 3 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0017 | 0/0 | 4315 | 2 | 1 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0018 | 0/0 | 4314 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0019 | 0/0 | 4314 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0021 | 0/0 | 4313 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0022 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0023 | 0/0 | 4310 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0027 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0028 | 0/0 | 4326 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0029 | 1/0 | 4310 | 1 | 0 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0030 | 0/0 | 4317 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0031 | 0/0 | 4320 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0032 | 0/0 | 4321 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0033 | 0/0 | 4324 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0034 | 0/0 | 4321 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0035 | 0/0 | 4326 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0036 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0037 | 0/0 | 4313 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0039 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0040 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0042 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0001t0044 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0005t0001 | 0/0 | 4324 | 3 | 0 | 3 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0008t0001 | 0/0 | 4324 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0009t0004 | 0/0 | 4321 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0001c0010t0002 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0001 | 0/0 | 4324 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0002 | 0/0 | 4313 | 4 | 4 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0005 | 0/0 | 4316 | 8 | 8 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0008 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0013 | 0/0 | 4317 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0017 | 0/0 | 4315 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0020 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0022 | 0/0 | 4314 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0024 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0026 | 0/0 | 4310 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0002c0002t0041 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0003c0003t0005 | 0/0 | 4316 | 3 | 0 | 0 | 1 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0003c0003t0013 | 0/0 | 4317 | 4 | 0 | 0 | 4 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0003c0003t0025 | 0/0 | 4317 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0004c0004t0002 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0004c0004t0007 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0004c0004t0011 | 0/0 | 4325 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0004c0004t0020 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0004c0004t0038 | 0/0 | 4313 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0004c0004t0043 | 0/0 | 4325 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0005c0006t0008 | 0/0 | 4314 | 3 | 0 | 1 | 2 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| a0006c0007t0002 | 0/0 | 4313 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | copy fasta | chr3 | 168003689 | 168100924 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0165 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0007g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0009g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0009g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0009g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0009g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0009g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0010g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0010g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0010g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0010g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0010g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0011g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0011g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0011g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0011g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0012g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0012g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0012g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0014g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0014g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0014g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0014g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0015g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0015g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0015g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0015g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0016g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0016g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0016g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0017g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0017g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0018g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0019g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0019g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0021g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0021g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0022g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0023g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0027g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0028g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0029g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0030g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0031g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0032g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0033g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0034g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0035g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0036g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0037g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0039g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0040g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0042g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0001t0044g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0005t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0005t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0005t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0008t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0009t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0001c0010t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0013g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0017g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0020g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0022g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0024g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0026g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0002c0002t0041g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0003c0003t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0003c0003t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0003c0003t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0003c0003t0013g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0003c0003t0013g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0003c0003t0013g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0003c0003t0013g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0003c0003t0025g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0004c0004t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0004c0004t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0004c0004t0011g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0004c0004t0020g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0004c0004t0038g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0004c0004t0043g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0005c0006t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0005c0006t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0005c0006t0008g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| a0006c0007t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0204 | EUR | GBR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00280 | hp1 | a0001 | c0009 | t0004 | g0064 | EUR | FIN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0095 | EUR | FIN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0163 | EUR | FIN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00558 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | CHS | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00558 | hp2 | a0001 | c0001 | t0044 | g0226 | EAS | CHS | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00642 | hp2 | a0001 | c0001 | t0011 | g0024 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01069 | hp1 | a0001 | c0001 | t0031 | g0091 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01069 | hp2 | a0001 | c0001 | t0009 | g0170 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0092 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0090 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01081 | hp2 | a0001 | c0005 | t0001 | g0178 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01106 | hp2 | a0001 | c0001 | t0010 | g0060 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01167 | hp1 | a0001 | c0001 | t0017 | g0142 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01169 | hp1 | a0001 | c0001 | t0014 | g0143 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01169 | hp2 | a0001 | c0001 | t0010 | g0023 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01175 | hp1 | a0001 | c0001 | t0006 | g0112 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01175 | hp2 | a0001 | c0001 | t0009 | g0029 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01192 | hp1 | a0001 | c0001 | t0015 | g0033 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01243 | hp1 | a0002 | c0002 | t0013 | g0108 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0036 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0147 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0030 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0146 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0062 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0086 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01361 | hp2 | a0006 | c0007 | t0002 | g0046 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01433 | hp1 | a0001 | c0001 | t0037 | g0213 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0135 | EUR | IBS | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01516 | hp2 | a0001 | c0001 | t0010 | g0043 | EUR | IBS | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0132 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01884 | hp2 | a0002 | c0002 | t0008 | g0121 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01891 | hp1 | a0001 | c0001 | t0035 | g0189 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0111 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01978 | hp1 | a0001 | c0001 | t0028 | g0040 | AMR | PEL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01978 | hp2 | a0001 | c0001 | t0011 | g0085 | AMR | PEL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01993 | hp1 | a0001 | c0005 | t0001 | g0074 | AMR | PEL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02004 | hp2 | a0001 | c0005 | t0001 | g0088 | AMR | PEL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02040 | hp1 | a0001 | c0001 | t0036 | g0157 | EAS | KHV | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02040 | hp2 | a0001 | c0008 | t0001 | g0015 | EAS | KHV | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02055 | hp1 | a0002 | c0002 | t0005 | g0104 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02055 | hp2 | a0002 | c0002 | t0041 | g0224 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02071 | hp1 | a0003 | c0003 | t0005 | g0145 | EAS | KHV | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02145 | hp1 | a0002 | c0002 | t0022 | g0221 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02145 | hp2 | a0001 | c0001 | t0019 | g0079 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0096 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02257 | hp2 | a0001 | c0001 | t0016 | g0003 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02258 | hp1 | a0001 | c0001 | t0012 | g0005 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02258 | hp2 | a0001 | c0001 | t0021 | g0220 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0007 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02451 | hp1 | a0001 | c0001 | t0022 | g0223 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0109 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0151 | EAS | KHV | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02523 | hp2 | a0003 | c0003 | t0013 | g0144 | EAS | KHV | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0022 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0099 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0004 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02630 | hp1 | a0002 | c0002 | t0005 | g0103 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02630 | hp2 | a0001 | c0010 | t0002 | g0083 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02683 | hp1 | a0001 | c0001 | t0011 | g0021 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02698 | hp1 | a0001 | c0001 | t0009 | g0202 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02698 | hp2 | a0001 | c0001 | t0034 | g0205 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02717 | hp1 | a0001 | c0001 | t0014 | g0102 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0131 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02723 | hp1 | a0002 | c0002 | t0005 | g0106 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02735 | hp2 | a0001 | c0001 | t0033 | g0093 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02809 | hp1 | a0002 | c0002 | t0005 | g0097 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02818 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02818 | hp2 | a0004 | c0004 | t0007 | g0141 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02886 | hp1 | a0001 | c0001 | t0023 | g0010 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02895 | hp2 | a0001 | c0001 | t0021 | g0218 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02896 | hp2 | a0001 | c0001 | t0018 | g0001 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02897 | hp1 | a0001 | c0001 | t0040 | g0219 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02897 | hp2 | a0001 | c0001 | t0018 | g0001 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02922 | hp1 | a0002 | c0002 | t0005 | g0140 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0201 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02965 | hp1 | a0004 | c0004 | t0011 | g0193 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0210 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0126 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02976 | hp2 | a0002 | c0002 | t0017 | g0107 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03041 | hp1 | a0002 | c0002 | t0026 | g0110 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03041 | hp2 | a0002 | c0002 | t0005 | g0124 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03098 | hp1 | a0001 | c0001 | t0030 | g0127 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0195 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03139 | hp1 | a0004 | c0004 | t0043 | g0225 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03139 | hp2 | a0001 | c0001 | t0039 | g0215 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0117 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0125 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03225 | hp1 | a0002 | c0002 | t0005 | g0105 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03225 | hp2 | a0002 | c0002 | t0024 | g0012 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0209 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03486 | hp2 | a0002 | c0002 | t0020 | g0216 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03490 | hp2 | a0001 | c0001 | t0010 | g0059 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03491 | hp1 | a0003 | c0003 | t0005 | g0197 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0123 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0084 | AFR | GWD | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03579 | hp1 | a0004 | c0004 | t0002 | g0139 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0160 | AFR | MSL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03654 | hp1 | a0001 | c0001 | t0015 | g0020 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03669 | hp1 | a0001 | c0001 | t0009 | g0134 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03669 | hp2 | a0001 | c0001 | t0015 | g0032 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG03710 | hp2 | a0003 | c0003 | t0005 | g0198 | SAS | PJL | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG04199 | hp1 | a0001 | c0001 | t0011 | g0190 | SAS | STU | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0054 | SAS | STU | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0206 | SAS | STU | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0006 | AFR | YRI | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0137 | AFR | YRI | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18906 | hp1 | a0004 | c0004 | t0020 | g0217 | AFR | YRI | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18906 | hp2 | a0001 | c0001 | t0012 | g0009 | AFR | YRI | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18942 | hp1 | a0001 | c0001 | t0010 | g0176 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18945 | hp2 | a0003 | c0003 | t0025 | g0013 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18956 | hp2 | a0005 | c0006 | t0008 | g0038 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18960 | hp2 | a0001 | c0001 | t0009 | g0052 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18971 | hp2 | a0001 | c0001 | t0032 | g0207 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18972 | hp1 | a0001 | c0001 | t0006 | g0075 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18972 | hp2 | a0005 | c0006 | t0008 | g0039 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18977 | hp2 | a0003 | c0003 | t0013 | g0199 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18994 | hp1 | a0003 | c0003 | t0013 | g0072 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19030 | hp1 | a0001 | c0001 | t0027 | g0118 | AFR | LWK | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0011 | AFR | LWK | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0122 | AFR | LWK | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19043 | hp2 | a0001 | c0001 | t0042 | g0222 | AFR | LWK | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19074 | hp2 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19085 | hp2 | a0001 | c0001 | t0006 | g0048 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19086 | hp1 | a0003 | c0003 | t0013 | g0150 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20129 | hp1 | a0001 | c0001 | t0019 | g0119 | AFR | ASW | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | ASW | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0016 | EUR | TSI | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0068 | EUR | TSI | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0156 | EUR | TSI | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | GIH | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | GIH | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01123 | hp1 | a0001 | c0001 | t0015 | g0089 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG01123 | hp2 | a0005 | c0006 | t0008 | g0133 | AMR | CLM | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02109 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02559 | hp1 | a0002 | c0002 | t0005 | g0212 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG06807 | hp1 | a0004 | c0004 | t0038 | g0214 | AFR | USA | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | USA | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | USA | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | USA | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0165 | REF | REF | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0029 | g0082 | REF | REF | GOLIM4_chr3_168003689_168100924 | GOLIM4 | chr3 | 168003689 | 168100924 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:168029234
|
C | T | 2 | a0003a0005 | 11 | HG01123.hp2 HG02071.hp1 HG02523.hp2 others(8): Show |
missense_variant | MODERATE | c.1502G>A | p.Gly501Glu | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/16 | 2141/4310 | 1502/2091 | 501/696 | chr3 | 168029234 | ||
| chr3:168029855
|
T | C | 1 | a0004 | 6 | HG02818.hp2 HG02965.hp1 HG03139.hp1 others(3): Show |
missense_variant | MODERATE | c.1358A>G | p.Gln453Arg | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 10/16 | 1997/4310 | 1358/2091 | 453/696 | chr3 | 168029855 | ||
| chr3:168029871
|
C | G | 2 | a0002a0003 | 29 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
missense_variant | MODERATE | c.1342G>C | p.Glu448Gln | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 10/16 | 1981/4310 | 1342/2091 | 448/696 | chr3 | 168029871 | ||
| chr3:168029919
|
C | T | 1 | a0006 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1294G>A | p.Glu432Lys | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 10/16 | 1933/4310 | 1294/2091 | 432/696 | chr3 | 168029919 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:168025024
|
G | A | 1 | a0001c0008 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.1695C>T | p.Ala565Ala | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 13/16 | 2334/4310 | 1695/2091 | 565/696 | chr3 | 168025024 | ||
| chr3:168029890
|
C | G | 1 | a0001c0005 | 3 | HG01081.hp2 HG01993.hp1 HG02004.hp2 |
synonymous_variant | LOW | c.1323G>C | p.Gly441Gly | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 10/16 | 1962/4310 | 1323/2091 | 441/696 | chr3 | 168029890 | ||
| chr3:168030001
|
T | C | 1 | a0001c0009 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.1212A>G | p.Gln404Gln | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 10/16 | 1851/4310 | 1212/2091 | 404/696 | chr3 | 168030001 | ||
| chr3:168032730
|
T | C | 1 | a0001c0010 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.966A>G | p.Gln322Gln | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/16 | 1605/4310 | 966/2091 | 322/696 | chr3 | 168032730 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:168008907
|
T | C | 1 | a0001c0001t0030 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1362A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 1362 | chr3 | 168008907 | |||||
| chr3:168008916
|
G | A | 1 | a0001c0001t0032 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1353C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 1353 | chr3 | 168008916 | |||||
| chr3:168008921
|
T | TA | 3 | a0001c0001t0014a0001c0001t0017a0002c0002t0017 | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1347dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 1347 | chr3 | 168008921 | |||||
| chr3:168009197
|
T | C | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1072A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 1072 | chr3 | 168009197 | |||||
| chr3:168009271
|
T | C | 1 | a0001c0001t0033 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 998 | chr3 | 168009271 | |||||
| chr3:168009425
|
T | TCAGA | 5 | a0001c0001t0016a0001c0001t0017a0001c0001t0019others(2): Show | 9 | HG01167.hp1 HG02145.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*843_*844insTCTG | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 843 | chr3 | 168009425 | |||||
| chr3:168009426
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0034 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*842_*843insTTTTTT others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 842 | chr3 | 168009426 | |||||
| chr3:168009426
|
C | CAGACA | 1 | a0001c0001t0014 | 4 | HG01169.hp1 HG02257.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*842_*843insTGTCT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 842 | chr3 | 168009426 | |||||
| chr3:168009427
|
A | AGAC | 17 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(14): Show | 55 | HG00280.hp2 HG00558.hp1 HG01175.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*841_*842insGTC | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 841 | chr3 | 168009427 | |||||
| chr3:168009430
|
C | A | 24 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(21): Show | 69 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*839G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 839 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAA | 7 | a0001c0001t0008a0001c0001t0018a0001c0001t0022others(4): Show | 14 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*835_*838dupTTTT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAAAA | 3 | a0001c0001t0005a0002c0002t0005a0003c0003t0005 | 14 | HG02055.hp1 HG02071.hp1 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*833_*838dupTTTTTT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAAAAA | 4 | a0001c0001t0030a0002c0002t0013a0003c0003t0013others(1): Show | 7 | HG01243.hp1 HG02523.hp2 HG03098.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*832_*838dupTTTTTT others(1): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0031 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*829_*838dupTTTTTT others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0004a0001c0001t0032a0001c0009t0004 | 21 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*828_*838dupTTTTTT others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0015 | 4 | HG01123.hp1 HG01192.hp1 HG03654.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*827_*838dupTTTTTT others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0009 | 7 | HG00323.hp1 HG01069.hp2 HG01175.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*826_*838dupTTTTTT others(7): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAAAAA others(7): Show |
9 | a0001c0001t0001a0001c0001t0003a0001c0001t0033others(6): Show | 73 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*825_*838dupTTTTTT others(8): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0010a0001c0001t0011a0004c0004t0011others(1): Show | 13 | HG00642.hp2 HG01106.hp2 HG01169.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*824_*838dupTTTTTT others(9): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009430
|
C | CAAAAAAA others(9): Show |
2 | a0001c0001t0028a0001c0001t0035 | 2 | HG01891.hp1 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*823_*838dupTTTTTT others(10): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 838 | chr3 | 168009430 | |||||
| chr3:168009482
|
G | A | 1 | a0001c0001t0036 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*787C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 787 | chr3 | 168009482 | |||||
| chr3:168009629
|
C | T | 3 | a0001c0001t0003a0001c0001t0010a0001c0001t0028 | 27 | HG00735.hp1 HG00741.hp2 HG01071.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*640G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 640 | chr3 | 168009629 | |||||
| chr3:168009648
|
C | T | 23 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(20): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*621G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 621 | chr3 | 168009648 | |||||
| chr3:168009682
|
T | C | 23 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(20): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*587A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 587 | chr3 | 168009682 | |||||
| chr3:168009783
|
G | A | 1 | a0001c0001t0006 | 10 | HG00558.hp1 HG01175.hp1 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*486C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 486 | chr3 | 168009783 | |||||
| chr3:168010096
|
C | T | 23 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(20): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*173G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 173 | chr3 | 168010096 | |||||
| chr3:168010266
|
C | T | 8 | a0001c0001t0008a0001c0001t0018a0001c0001t0022others(5): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 3 | chr3 | 168010266 | |||||
| chr3:168010267
|
C | T | 3 | a0001c0001t0007a0004c0004t0007a0004c0004t0038 | 10 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 16/16 | 2 | chr3 | 168010267 | |||||
| chr3:168095334
|
T | C | 1 | a0001c0001t0037 | 1 | HG01433.hp1 | 5_prime_UTR_variant | MODIFIER | c.-49A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/16 | 49 | chr3 | 168095334 | |||||
| chr3:168095429
|
G | T | 1 | a0003c0003t0025 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-144C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/16 | 144 | chr3 | 168095429 | |||||
| chr3:168095466
|
G | A | 2 | a0001c0001t0039a0004c0004t0038 | 2 | HG03139.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-181C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/16 | 181 | chr3 | 168095466 | |||||
| chr3:168095490
|
C | T | 2 | a0001c0001t0018a0002c0002t0024 | 3 | HG02896.hp2 HG02897.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-205G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/16 | 205 | chr3 | 168095490 | |||||
| chr3:168095594
|
G | A | 2 | a0002c0002t0020a0004c0004t0020 | 2 | HG03486.hp2 NA18906.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-309C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/16 | chr3 | 168095594 | ||||||
| chr3:168095645
|
G | A | 2 | a0001c0001t0021a0001c0001t0040 | 3 | HG02258.hp2 HG02895.hp2 HG02897.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-360C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/16 | chr3 | 168095645 | ||||||
| chr3:168095656
|
G | A | 5 | a0001c0001t0022a0001c0001t0042a0002c0002t0022others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-371C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/16 | 371 | chr3 | 168095656 | |||||
| chr3:168095832
|
G | T | 3 | a0001c0001t0012a0001c0001t0016a0001c0001t0023 | 9 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-547C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/16 | 547 | chr3 | 168095832 | |||||
| chr3:168095914
|
G | A | 1 | a0001c0001t0044 | 1 | HG00558.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-629C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/16 | chr3 | 168095914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:168010466
|
G | A | 14 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(11): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1942-48C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 15/15 | chr3 | 168010466 | ||||||
| chr3:168010518
|
GA | G | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1942-101delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 15/15 | chr3 | 168010518 | ||||||
| chr3:168010657
|
G | C | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1941+86C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 15/15 | chr3 | 168010657 | ||||||
| chr3:168010840
|
A | G | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861-17T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168010840 | ||||||
| chr3:168010857
|
T | C | 3 | a0001c0001t0012g0005a0001c0001t0012g0006a0001c0001t0012g0007 | 3 | HG02258.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1861-34A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168010857 | ||||||
| chr3:168010875
|
C | T | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-52G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168010875 | ||||||
| chr3:168010908
|
G | C | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-85C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168010908 | ||||||
| chr3:168010911
|
T | C | 1 | a0001c0001t0003g0076 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1861-88A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168010911 | ||||||
| chr3:168011020
|
A | T | 27 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1861-197T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011020 | ||||||
| chr3:168011091
|
G | A | 8 | a0002c0002t0005g0097a0002c0002t0005g0103a0002c0002t0005g0104others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-268C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011091 | ||||||
| chr3:168011103
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-280T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011103 | ||||||
| chr3:168011139
|
C | A | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-316G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011139 | ||||||
| chr3:168011185
|
C | T | 14 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(11): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1861-362G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011185 | ||||||
| chr3:168011186
|
G | A | 1 | a0001c0008t0001g0015 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1861-363C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011186 | ||||||
| chr3:168011191
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-368T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011191 | ||||||
| chr3:168011202
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-379T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011202 | ||||||
| chr3:168011220
|
G | A | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-397C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011220 | ||||||
| chr3:168011221
|
T | C | 131 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1861-398A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011221 | ||||||
| chr3:168011246
|
G | A | 99 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(96): Show | 100 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(97): Show |
intron_variant | MODIFIER | c.1861-423C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011246 | ||||||
| chr3:168011302
|
C | G | 131 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1861-479G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011302 | ||||||
| chr3:168011336
|
G | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-513C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011336 | ||||||
| chr3:168011351
|
C | T | 27 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1861-528G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011351 | ||||||
| chr3:168011372
|
G | A | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-549C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011372 | ||||||
| chr3:168011409
|
G | A | 71 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(68): Show | 71 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(68): Show |
intron_variant | MODIFIER | c.1861-586C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011409 | ||||||
| chr3:168011410
|
C | A | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-587G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011410 | ||||||
| chr3:168011426
|
C | A | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-603G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011426 | ||||||
| chr3:168011449
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1861-626G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011449 | ||||||
| chr3:168011456
|
A | G | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1861-633T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011456 | ||||||
| chr3:168011462
|
G | C | 1 | a0001c0001t0004g0028 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1861-639C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011462 | ||||||
| chr3:168011490
|
C | T | 2 | a0001c0001t0004g0204a0001c0001t0015g0020 | 2 | HG00140.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1861-667G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011490 | ||||||
| chr3:168011494
|
A | C | 2 | a0001c0001t0004g0204a0001c0001t0015g0020 | 2 | HG00140.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1861-671T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011494 | ||||||
| chr3:168011512
|
T | C | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-689A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011512 | ||||||
| chr3:168011524
|
A | C | 14 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(11): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1861-701T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011524 | ||||||
| chr3:168011531
|
C | T | 14 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(11): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1861-708G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011531 | ||||||
| chr3:168011552
|
G | A | 27 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1861-729C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011552 | ||||||
| chr3:168011703
|
G | A | 27 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1861-880C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011703 | ||||||
| chr3:168011703
|
G | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0173a0001c0001t0011g0126 | 3 | HG00140.hp2 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1861-880C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011703 | ||||||
| chr3:168011732
|
GACCCCTT | G | 67 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(64): Show | 67 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.1861-916_1861-910d others(9): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011732 | ||||||
| chr3:168011733
|
AC | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-911delG | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011733 | ||||||
| chr3:168011739
|
T | G | 37 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(34): Show | 38 | HG01123.hp2 HG01243.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.1861-916A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011739 | ||||||
| chr3:168011779
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-956T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011779 | ||||||
| chr3:168011798
|
A | C | 71 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(68): Show | 71 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(68): Show |
intron_variant | MODIFIER | c.1861-975T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011798 | ||||||
| chr3:168011799
|
G | A | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-976C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011799 | ||||||
| chr3:168011844
|
G | C | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1861-1021C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011844 | ||||||
| chr3:168011920
|
C | T | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1861-1097G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011920 | ||||||
| chr3:168011962
|
T | C | 14 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(11): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1861-1139A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011962 | ||||||
| chr3:168011983
|
G | A | 1 | a0002c0002t0017g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1861-1160C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011983 | ||||||
| chr3:168011997
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-1174T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168011997 | ||||||
| chr3:168012024
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-1201T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012024 | ||||||
| chr3:168012049
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-1226T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012049 | ||||||
| chr3:168012055
|
G | A | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1861-1232C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012055 | ||||||
| chr3:168012062
|
G | GAGA | 131 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1861-1242_1861-124 others(7): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012062 | ||||||
| chr3:168012070
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-1247A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012070 | ||||||
| chr3:168012139
|
G | GAA | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-1318_1861-131 others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012139 | ||||||
| chr3:168012156
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-1333T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012156 | ||||||
| chr3:168012233
|
A | G | 131 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1861-1410T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012233 | ||||||
| chr3:168012244
|
A | G | 7 | a0001c0001t0003g0022a0001c0001t0003g0054a0001c0001t0003g0055others(4): Show | 7 | HG02602.hp2 HG02735.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1861-1421T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012244 | ||||||
| chr3:168012258
|
C | T | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1861-1435G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012258 | ||||||
| chr3:168012274
|
T | G | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1861-1451A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012274 | ||||||
| chr3:168012319
|
C | T | 77 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(74): Show | 77 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.1861-1496G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012319 | ||||||
| chr3:168012326
|
A | G | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1861-1503T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012326 | ||||||
| chr3:168012387
|
T | C | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-1564A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012387 | ||||||
| chr3:168012413
|
A | T | 1 | a0001c0001t0003g0056 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1861-1590T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012413 | ||||||
| chr3:168012451
|
T | C | 9 | a0001c0001t0001g0162a0003c0003t0005g0145a0003c0003t0005g0197others(6): Show | 9 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-1628A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012451 | ||||||
| chr3:168012513
|
C | T | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-1690G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012513 | ||||||
| chr3:168012520
|
A | G | 3 | a0001c0001t0016g0003a0001c0001t0016g0004a0001c0001t0019g0119 | 3 | HG02257.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1861-1697T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012520 | ||||||
| chr3:168012550
|
T | C | 1 | a0001c0001t0033g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1861-1727A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012550 | ||||||
| chr3:168012565
|
C | G | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1861-1742G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012565 | ||||||
| chr3:168012610
|
A | C | 1 | a0001c0001t0004g0156 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1861-1787T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012610 | ||||||
| chr3:168012684
|
G | A | 7 | a0001c0001t0002g0034a0001c0001t0019g0079a0001c0001t0037g0213others(4): Show | 7 | HG01243.hp2 HG01433.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1861-1861C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012684 | ||||||
| chr3:168012738
|
C | T | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861-1915G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012738 | ||||||
| chr3:168012818
|
C | A | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1861-1995G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012818 | ||||||
| chr3:168012868
|
C | G | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-2045G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012868 | ||||||
| chr3:168012882
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-2059T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012882 | ||||||
| chr3:168012891
|
G | A | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1861-2068C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012891 | ||||||
| chr3:168012905
|
G | C | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-2082C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012905 | ||||||
| chr3:168012943
|
T | A | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-2120A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168012943 | ||||||
| chr3:168013022
|
G | C | 131 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1861-2199C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013022 | ||||||
| chr3:168013059
|
T | C | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-2236A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013059 | ||||||
| chr3:168013152
|
G | C | 23 | a0001c0001t0002g0120a0001c0001t0002g0136a0001c0001t0002g0174others(20): Show | 23 | HG00558.hp1 HG01175.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1861-2329C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013152 | ||||||
| chr3:168013221
|
A | G | 58 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(55): Show | 58 | HG00280.hp2 HG00558.hp1 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.1861-2398T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013221 | ||||||
| chr3:168013429
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0011g0024 | 2 | HG00642.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1861-2606C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013429 | ||||||
| chr3:168013493
|
TC | T | 35 | a0001c0001t0002g0027a0001c0001t0002g0078a0001c0001t0002g0095others(32): Show | 35 | HG00280.hp2 HG00558.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.1861-2671delG | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013493 | ||||||
| chr3:168013535
|
C | T | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-2712G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013535 | ||||||
| chr3:168013537
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-2714T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013537 | ||||||
| chr3:168013544
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-2721A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013544 | ||||||
| chr3:168013639
|
AG | A | 12 | a0001c0001t0002g0027a0001c0001t0002g0078a0001c0001t0002g0095others(9): Show | 12 | HG00280.hp2 HG01361.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1861-2817delC | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013639 | ||||||
| chr3:168013730
|
G | T | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-2907C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013730 | ||||||
| chr3:168013744
|
A | G | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-2921T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013744 | ||||||
| chr3:168013747
|
G | T | 1 | a0004c0004t0043g0225 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1861-2924C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013747 | ||||||
| chr3:168013758
|
T | C | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861-2935A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013758 | ||||||
| chr3:168013784
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG00323.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1861-2961A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013784 | ||||||
| chr3:168013788
|
T | A | 99 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(96): Show | 100 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(97): Show |
intron_variant | MODIFIER | c.1861-2965A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013788 | ||||||
| chr3:168013792
|
G | A | 1 | a0001c0001t0004g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1861-2969C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013792 | ||||||
| chr3:168013856
|
A | C | 1 | a0002c0002t0024g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1861-3033T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013856 | ||||||
| chr3:168013878
|
G | A | 11 | a0001c0001t0002g0078a0001c0001t0002g0095a0003c0003t0005g0145others(8): Show | 11 | HG00280.hp2 HG01361.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1861-3055C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168013878 | ||||||
| chr3:168014057
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-3234T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014057 | ||||||
| chr3:168014058
|
A | T | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-3235T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014058 | ||||||
| chr3:168014059
|
A | T | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-3236T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014059 | ||||||
| chr3:168014103
|
T | C | 1 | a0001c0001t0006g0086 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1861-3280A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014103 | ||||||
| chr3:168014138
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG00323.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1861-3315C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014138 | ||||||
| chr3:168014217
|
G | A | 1 | a0001c0001t0030g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1861-3394C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014217 | ||||||
| chr3:168014268
|
A | G | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-3445T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014268 | ||||||
| chr3:168014312
|
C | CACATACA others(85): Show |
1 | a0001c0001t0002g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1861-3581_1861-349 others(96): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014312 | ||||||
| chr3:168014357
|
G | T | 14 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(11): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1861-3534C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014357 | ||||||
| chr3:168014385
|
G | A | 7 | a0001c0001t0014g0096a0001c0001t0014g0102a0001c0001t0014g0117others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1861-3562C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014385 | ||||||
| chr3:168014402
|
C | G | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861-3579G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014402 | ||||||
| chr3:168014406
|
C | T | 10 | a0001c0001t0008g0099a0001c0001t0008g0101a0001c0001t0008g0125others(7): Show | 11 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1861-3583G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014406 | ||||||
| chr3:168014445
|
G | A | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1861-3622C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014445 | ||||||
| chr3:168014554
|
T | A | 1 | a0001c0001t0037g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1861-3731A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014554 | ||||||
| chr3:168014561
|
A | AC | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-3739dupG | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014561 | ||||||
| chr3:168014591
|
A | G | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1861-3768T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014591 | ||||||
| chr3:168014602
|
A | G | 7 | a0001c0001t0014g0096a0001c0001t0014g0102a0001c0001t0014g0117others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1861-3779T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014602 | ||||||
| chr3:168014656
|
A | C | 1 | a0001c0001t0007g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1861-3833T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014656 | ||||||
| chr3:168014662
|
A | C | 1 | a0001c0001t0007g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1861-3839T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014662 | ||||||
| chr3:168014667
|
A | G | 1 | a0002c0002t0005g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1861-3844T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014667 | ||||||
| chr3:168014739
|
G | A | 12 | a0001c0001t0007g0160a0001c0001t0008g0099a0001c0001t0008g0101others(9): Show | 13 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1861-3916C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014739 | ||||||
| chr3:168014994
|
C | T | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1861-4171G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168014994 | ||||||
| chr3:168015049
|
G | T | 27 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1861-4226C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015049 | ||||||
| chr3:168015127
|
A | G | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861-4304T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015127 | ||||||
| chr3:168015235
|
A | T | 7 | a0001c0001t0014g0096a0001c0001t0014g0102a0001c0001t0014g0117others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1861-4412T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015235 | ||||||
| chr3:168015236
|
C | T | 131 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1861-4413G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015236 | ||||||
| chr3:168015386
|
A | G | 2 | a0002c0002t0005g0140a0002c0002t0005g0212 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1861-4563T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015386 | ||||||
| chr3:168015442
|
TATC | T | 14 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(11): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1861-4622_1861-462 others(7): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015442 | ||||||
| chr3:168015446
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-4623T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015446 | ||||||
| chr3:168015512
|
C | A | 20 | a0001c0001t0002g0174a0001c0001t0006g0017a0001c0001t0006g0048others(17): Show | 20 | HG00558.hp1 HG01175.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1861-4689G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015512 | ||||||
| chr3:168015573
|
G | A | 56 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(53): Show | 56 | HG00280.hp2 HG00558.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.1861-4750C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015573 | ||||||
| chr3:168015577
|
C | T | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-4754G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015577 | ||||||
| chr3:168015620
|
A | AC | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-4798dupG | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015620 | ||||||
| chr3:168015688
|
G | C | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-4865C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015688 | ||||||
| chr3:168015694
|
T | G | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-4871A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015694 | ||||||
| chr3:168015706
|
G | C | 3 | a0001c0001t0002g0208a0001c0001t0012g0008a0001c0001t0012g0009 | 3 | HG02109.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1861-4883C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015706 | ||||||
| chr3:168015732
|
C | T | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-4909G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015732 | ||||||
| chr3:168015734
|
T | C | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-4911A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015734 | ||||||
| chr3:168015735
|
C | T | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-4912G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015735 | ||||||
| chr3:168015814
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1861-4991C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015814 | ||||||
| chr3:168015840
|
G | A | 2 | a0001c0001t0001g0073a0001c0008t0001g0015 | 2 | HG02040.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1861-5017C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015840 | ||||||
| chr3:168015861
|
A | C | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1861-5038T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015861 | ||||||
| chr3:168015913
|
C | T | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-5090G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015913 | ||||||
| chr3:168015927
|
C | T | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861-5104G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015927 | ||||||
| chr3:168015937
|
C | T | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-5114G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015937 | ||||||
| chr3:168015940
|
G | A | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1861-5117C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168015940 | ||||||
| chr3:168016017
|
C | T | 66 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(63): Show | 66 | HG00280.hp2 HG00558.hp1 HG01175.hp1 others(63): Show |
intron_variant | MODIFIER | c.1861-5194G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016017 | ||||||
| chr3:168016032
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-5209A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016032 | ||||||
| chr3:168016041
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1861-5218C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016041 | ||||||
| chr3:168016079
|
C | G | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5256G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016079 | ||||||
| chr3:168016103
|
A | C | 3 | a0002c0002t0002g0209a0002c0002t0002g0210a0002c0002t0041g0224 | 3 | HG02055.hp2 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1861-5280T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016103 | ||||||
| chr3:168016144
|
T | C | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861-5321A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016144 | ||||||
| chr3:168016151
|
T | G | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5328A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016151 | ||||||
| chr3:168016195
|
G | C | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5372C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016195 | ||||||
| chr3:168016208
|
A | C | 1 | a0001c0001t0006g0169 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1861-5385T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016208 | ||||||
| chr3:168016243
|
A | G | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5420T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016243 | ||||||
| chr3:168016358
|
G | C | 31 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(28): Show | 32 | HG01123.hp2 HG01243.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1861-5535C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016358 | ||||||
| chr3:168016425
|
C | T | 1 | a0002c0002t0005g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1861-5602G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016425 | ||||||
| chr3:168016426
|
G | A | 87 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(84): Show | 88 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(85): Show |
intron_variant | MODIFIER | c.1861-5603C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016426 | ||||||
| chr3:168016456
|
A | G | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5633T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016456 | ||||||
| chr3:168016507
|
G | A | 74 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(71): Show | 74 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(71): Show |
intron_variant | MODIFIER | c.1861-5684C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016507 | ||||||
| chr3:168016534
|
C | A | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5711G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016534 | ||||||
| chr3:168016555
|
G | T | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5732C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016555 | ||||||
| chr3:168016558
|
T | C | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5735A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016558 | ||||||
| chr3:168016563
|
A | T | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5740T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016563 | ||||||
| chr3:168016592
|
T | C | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5769A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016592 | ||||||
| chr3:168016593
|
G | A | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5770C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016593 | ||||||
| chr3:168016605
|
T | C | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5782A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016605 | ||||||
| chr3:168016686
|
T | G | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1861-5863A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016686 | ||||||
| chr3:168016702
|
C | A | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1861-5879G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016702 | ||||||
| chr3:168016710
|
C | A | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861-5887G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016710 | ||||||
| chr3:168016720
|
G | T | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5897C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016720 | ||||||
| chr3:168016721
|
T | G | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-5898A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016721 | ||||||
| chr3:168016900
|
A | G | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1861-6077T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016900 | ||||||
| chr3:168016909
|
C | G | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1861-6086G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016909 | ||||||
| chr3:168016927
|
A | G | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1861-6104T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168016927 | ||||||
| chr3:168017087
|
A | C | 7 | a0001c0001t0014g0096a0001c0001t0014g0102a0001c0001t0014g0117others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1861-6264T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017087 | ||||||
| chr3:168017214
|
G | A | 14 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(11): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1861-6391C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017214 | ||||||
| chr3:168017250
|
G | C | 1 | a0002c0002t0008g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1861-6427C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017250 | ||||||
| chr3:168017383
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1861-6560G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017383 | ||||||
| chr3:168017427
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-6604A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017427 | ||||||
| chr3:168017454
|
C | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861-6631G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017454 | ||||||
| chr3:168017465
|
C | G | 2 | a0004c0004t0011g0193a0004c0004t0043g0225 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1861-6642G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017465 | ||||||
| chr3:168017754
|
G | A | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+6772C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017754 | ||||||
| chr3:168017825
|
C | CCT | 17 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1860+6699_1860+670 others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017825 | ||||||
| chr3:168017954
|
T | C | 7 | a0001c0001t0014g0096a0001c0001t0014g0102a0001c0001t0014g0117others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1860+6572A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017954 | ||||||
| chr3:168017965
|
T | C | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1860+6561A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168017965 | ||||||
| chr3:168018073
|
A | C | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1860+6453T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018073 | ||||||
| chr3:168018098
|
A | G | 1 | a0003c0003t0013g0150 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1860+6428T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018098 | ||||||
| chr3:168018100
|
C | T | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1860+6426G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018100 | ||||||
| chr3:168018141
|
G | C | 7 | a0001c0001t0014g0096a0001c0001t0014g0102a0001c0001t0014g0117others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1860+6385C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018141 | ||||||
| chr3:168018144
|
C | CTT | 10 | a0001c0001t0008g0099a0001c0001t0008g0101a0001c0001t0008g0125others(7): Show | 11 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1860+6380_1860+638 others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018144 | ||||||
| chr3:168018252
|
A | G | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1860+6274T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018252 | ||||||
| chr3:168018291
|
G | A | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1860+6235C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018291 | ||||||
| chr3:168018304
|
G | A | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1860+6222C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018304 | ||||||
| chr3:168018452
|
C | T | 1 | a0001c0001t0006g0112 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1860+6074G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018452 | ||||||
| chr3:168018516
|
C | T | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1860+6010G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018516 | ||||||
| chr3:168018538
|
T | C | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+5988A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018538 | ||||||
| chr3:168018595
|
T | C | 3 | a0001c0001t0016g0003a0001c0001t0016g0004a0001c0001t0019g0119 | 3 | HG02257.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1860+5931A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018595 | ||||||
| chr3:168018602
|
C | T | 6 | a0001c0001t0001g0087a0001c0001t0001g0152a0001c0001t0001g0177others(3): Show | 6 | HG00738.hp1 HG01069.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1860+5924G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018602 | ||||||
| chr3:168018622
|
G | A | 11 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(8): Show | 12 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1860+5904C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018622 | ||||||
| chr3:168018652
|
A | G | 1 | a0001c0005t0001g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1860+5874T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018652 | ||||||
| chr3:168018665
|
C | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1860+5861G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018665 | ||||||
| chr3:168018669
|
G | T | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1860+5857C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018669 | ||||||
| chr3:168018690
|
T | C | 17 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1860+5836A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018690 | ||||||
| chr3:168018718
|
T | C | 1 | a0002c0002t0026g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1860+5808A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018718 | ||||||
| chr3:168018774
|
C | T | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+5752G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018774 | ||||||
| chr3:168018832
|
G | A | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+5694C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018832 | ||||||
| chr3:168018857
|
G | A | 65 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(62): Show | 65 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(62): Show |
intron_variant | MODIFIER | c.1860+5669C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018857 | ||||||
| chr3:168018912
|
C | T | 14 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(11): Show | 15 | HG01123.hp2 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1860+5614G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018912 | ||||||
| chr3:168018916
|
T | C | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+5610A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018916 | ||||||
| chr3:168018983
|
C | CAA | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+5541_1860+554 others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018983 | ||||||
| chr3:168018990
|
A | T | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1860+5536T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168018990 | ||||||
| chr3:168019103
|
A | G | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1860+5423T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019103 | ||||||
| chr3:168019218
|
G | A | 7 | a0001c0001t0014g0096a0001c0001t0014g0102a0001c0001t0014g0117others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1860+5308C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019218 | ||||||
| chr3:168019315
|
T | G | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+5211A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019315 | ||||||
| chr3:168019364
|
G | A | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1860+5162C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019364 | ||||||
| chr3:168019464
|
A | G | 104 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(101): Show | 105 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(102): Show |
intron_variant | MODIFIER | c.1860+5062T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019464 | ||||||
| chr3:168019686
|
T | C | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1860+4840A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019686 | ||||||
| chr3:168019763
|
C | T | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+4763G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019763 | ||||||
| chr3:168019953
|
C | CA | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1860+4572dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019953 | ||||||
| chr3:168019953
|
CA | C | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+4572delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019953 | ||||||
| chr3:168019973
|
G | C | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+4553C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019973 | ||||||
| chr3:168019983
|
T | C | 90 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(87): Show | 90 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(87): Show |
intron_variant | MODIFIER | c.1860+4543A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019983 | ||||||
| chr3:168019984
|
G | A | 73 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(70): Show | 73 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(70): Show |
intron_variant | MODIFIER | c.1860+4542C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168019984 | ||||||
| chr3:168020025
|
C | T | 99 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(96): Show | 100 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(97): Show |
intron_variant | MODIFIER | c.1860+4501G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168020025 | ||||||
| chr3:168020311
|
G | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1860+4215C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168020311 | ||||||
| chr3:168020387
|
G | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1860+4139C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168020387 | ||||||
| chr3:168020391
|
G | A | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1860+4135C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168020391 | ||||||
| chr3:168020409
|
C | T | 10 | a0001c0001t0014g0096a0001c0001t0014g0102a0001c0001t0014g0117others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1860+4117G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168020409 | ||||||
| chr3:168020732
|
A | G | 68 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(65): Show | 68 | HG00280.hp2 HG00558.hp1 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.1860+3794T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168020732 | ||||||
| chr3:168020750
|
C | T | 9 | a0001c0001t0002g0120a0001c0001t0002g0136a0001c0001t0002g0208others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1860+3776G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168020750 | ||||||
| chr3:168020847
|
T | C | 5 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(2): Show | 5 | HG02486.hp2 HG02886.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1860+3679A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168020847 | ||||||
| chr3:168020939
|
T | C | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1860+3587A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168020939 | ||||||
| chr3:168021059
|
T | C | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1860+3467A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168021059 | ||||||
| chr3:168021181
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1860+3345A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168021181 | ||||||
| chr3:168021195
|
C | A | 1 | a0001c0001t0019g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1860+3331G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168021195 | ||||||
| chr3:168021418
|
C | A | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1860+3108G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168021418 | ||||||
| chr3:168021490
|
A | C | 1 | a0001c0001t0015g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1860+3036T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168021490 | ||||||
| chr3:168021984
|
C | T | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1860+2542G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168021984 | ||||||
| chr3:168022236
|
T | G | 1 | a0002c0002t0024g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1860+2290A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168022236 | ||||||
| chr3:168022261
|
G | A | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1860+2265C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168022261 | ||||||
| chr3:168022296
|
C | T | 18 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(15): Show | 19 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1860+2230G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168022296 | ||||||
| chr3:168022333
|
TA | T | 12 | a0001c0001t0005g0115a0001c0001t0005g0137a0001c0001t0005g0201others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1860+2192delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168022333 | ||||||
| chr3:168022333
|
TAA | T | 21 | a0001c0001t0008g0098a0001c0001t0030g0127a0002c0002t0005g0097others(18): Show | 21 | HG01123.hp2 HG01243.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1860+2191_1860+219 others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168022333 | ||||||
| chr3:168022344
|
A | C | 7 | a0001c0001t0016g0003a0001c0001t0016g0004a0001c0001t0019g0119others(4): Show | 7 | HG01123.hp2 HG01993.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1860+2182T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168022344 | ||||||
| chr3:168022397
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0058a0001c0001t0001g0168others(1): Show | 4 | NA18942.hp2 NA18956.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1860+2129A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168022397 | ||||||
| chr3:168022634
|
C | G | 10 | a0001c0001t0030g0127a0002c0002t0002g0109a0002c0002t0005g0097others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1860+1892G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168022634 | ||||||
| chr3:168023451
|
A | G | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1860+1075T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168023451 | ||||||
| chr3:168023570
|
T | C | 13 | a0001c0001t0002g0027a0001c0001t0002g0078a0001c0001t0002g0095others(10): Show | 13 | HG00280.hp2 HG01361.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1860+956A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168023570 | ||||||
| chr3:168023594
|
A | T | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1860+932T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168023594 | ||||||
| chr3:168023762
|
T | C | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1860+764A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168023762 | ||||||
| chr3:168023798
|
C | T | 3 | a0001c0001t0016g0003a0001c0001t0016g0004a0001c0001t0019g0119 | 3 | HG02257.hp2 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1860+728G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168023798 | ||||||
| chr3:168023882
|
G | A | 10 | a0001c0001t0002g0174a0001c0001t0006g0017a0001c0001t0006g0048others(7): Show | 10 | HG00558.hp1 HG01175.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1860+644C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168023882 | ||||||
| chr3:168023882
|
G | C | 3 | a0001c0001t0002g0034a0001c0001t0019g0079a0001c0001t0037g0213 | 3 | HG01243.hp2 HG01433.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1860+644C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168023882 | ||||||
| chr3:168023898
|
TAAC | T | 9 | a0001c0001t0030g0127a0002c0002t0005g0097a0002c0002t0005g0103others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1860+625_1860+627d others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168023898 | ||||||
| chr3:168024213
|
G | C | 10 | a0001c0001t0008g0099a0001c0001t0008g0101a0001c0001t0008g0125others(7): Show | 11 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1860+313C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168024213 | ||||||
| chr3:168024227
|
T | C | 10 | a0001c0001t0030g0127a0002c0002t0002g0109a0002c0002t0005g0097others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1860+299A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168024227 | ||||||
| chr3:168024341
|
C | G | 1 | a0002c0002t0005g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1860+185G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168024341 | ||||||
| chr3:168024460
|
G | A | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1860+66C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 14/15 | chr3 | 168024460 | ||||||
| chr3:168024880
|
C | T | 1 | a0002c0002t0005g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1791+48G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 13/15 | chr3 | 168024880 | ||||||
| chr3:168025154
|
C | T | 2 | a0003c0003t0005g0197a0003c0003t0005g0198 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1624-59G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168025154 | ||||||
| chr3:168025201
|
C | T | 10 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0084others(7): Show | 10 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1624-106G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168025201 | ||||||
| chr3:168025250
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1624-155T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168025250 | ||||||
| chr3:168025404
|
T | C | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1624-309A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168025404 | ||||||
| chr3:168025412
|
A | T | 7 | a0001c0001t0014g0096a0001c0001t0014g0102a0001c0001t0014g0117others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1624-317T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168025412 | ||||||
| chr3:168025454
|
TG | T | 56 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(53): Show | 56 | HG00280.hp2 HG00558.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.1624-360delC | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168025454 | ||||||
| chr3:168025568
|
G | A | 1 | a0002c0002t0024g0012 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1624-473C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168025568 | ||||||
| chr3:168025721
|
G | C | 1 | a0001c0001t0010g0059 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1624-626C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168025721 | ||||||
| chr3:168025973
|
G | C | 127 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(124): Show | 128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.1624-878C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168025973 | ||||||
| chr3:168026097
|
CTTGAACA others(3): Show |
C | 1 | a0002c0002t0017g0107 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1624-1012_1624-100 others(14): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168026097 | ||||||
| chr3:168026111
|
A | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0061 | 3 | HG00099.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1624-1016T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168026111 | ||||||
| chr3:168026250
|
A | ATC | 71 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(68): Show | 71 | HG00280.hp2 HG00558.hp1 HG01175.hp1 others(68): Show |
intron_variant | MODIFIER | c.1624-1157_1624-115 others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168026250 | ||||||
| chr3:168026310
|
A | C | 27 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(24): Show | 27 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1624-1215T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168026310 | ||||||
| chr3:168026360
|
C | T | 1 | a0002c0002t0005g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1624-1265G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168026360 | ||||||
| chr3:168026461
|
G | A | 9 | a0001c0001t0002g0120a0001c0001t0002g0136a0001c0001t0002g0208others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1623+1267C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168026461 | ||||||
| chr3:168026525
|
A | G | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.1623+1203T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168026525 | ||||||
| chr3:168026719
|
A | T | 100 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0069others(97): Show | 101 | HG00280.hp2 HG00558.hp1 HG01123.hp2 others(98): Show |
intron_variant | MODIFIER | c.1623+1009T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168026719 | ||||||
| chr3:168026876
|
T | C | 3 | a0001c0001t0011g0126a0004c0004t0011g0193a0004c0004t0043g0225 | 3 | HG02965.hp1 HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1623+852A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168026876 | ||||||
| chr3:168027109
|
G | C | 10 | a0001c0001t0008g0099a0001c0001t0008g0101a0001c0001t0008g0125others(7): Show | 11 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1623+619C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168027109 | ||||||
| chr3:168027115
|
T | C | 1 | a0001c0001t0030g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1623+613A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168027115 | ||||||
| chr3:168027116
|
C | CA | 10 | a0001c0001t0030g0127a0002c0002t0002g0109a0002c0002t0005g0097others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1623+611dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168027116 | ||||||
| chr3:168027465
|
C | G | 1 | a0001c0001t0003g0056 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1623+263G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168027465 | ||||||
| chr3:168027478
|
G | GA | 67 | a0001c0001t0001g0047a0001c0001t0002g0034a0001c0001t0002g0069others(64): Show | 67 | HG00280.hp2 HG00558.hp1 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.1623+249dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168027478 | ||||||
| chr3:168027499
|
GT | G | 22 | a0001c0001t0008g0098a0001c0001t0011g0126a0001c0001t0014g0096others(19): Show | 22 | HG01123.hp2 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1623+228delA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168027499 | ||||||
| chr3:168027612
|
G | A | 14 | a0001c0001t0001g0042a0001c0001t0003g0019a0001c0001t0003g0041others(11): Show | 14 | HG00735.hp1 HG00741.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1623+116C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 12/15 | chr3 | 168027612 | ||||||
| chr3:168027842
|
C | A | 6 | a0001c0001t0007g0130a0004c0004t0002g0139a0004c0004t0011g0193others(3): Show | 6 | HG02486.hp1 HG02965.hp1 HG03139.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1514-5G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168027842 | ||||||
| chr3:168027904
|
G | A | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1514-67C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168027904 | ||||||
| chr3:168027906
|
AAAGCCAC others(6): Show |
A | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1514-82_1514-70del others(13): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168027906 | ||||||
| chr3:168027915
|
A | G | 21 | a0001c0001t0002g0174a0001c0001t0004g0028a0001c0001t0004g0030others(18): Show | 21 | HG00140.hp1 HG00280.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1514-78T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168027915 | ||||||
| chr3:168027933
|
C | A | 8 | a0001c0001t0002g0159a0001c0001t0007g0160a0001c0001t0014g0096others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1514-96G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168027933 | ||||||
| chr3:168028010
|
C | A | 15 | a0001c0001t0030g0127a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1514-173G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168028010 | ||||||
| chr3:168028186
|
T | C | 5 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1514-349A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168028186 | ||||||
| chr3:168028293
|
A | G | 1 | a0002c0002t0005g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1514-456T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168028293 | ||||||
| chr3:168028430
|
A | G | 19 | a0001c0001t0008g0098a0002c0002t0001g0211a0002c0002t0002g0209others(16): Show | 19 | HG01123.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1514-593T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168028430 | ||||||
| chr3:168028494
|
T | A | 14 | a0002c0002t0002g0109a0002c0002t0002g0123a0002c0002t0005g0097others(11): Show | 14 | HG01243.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1514-657A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168028494 | ||||||
| chr3:168028504
|
G | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(60): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1514-667C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168028504 | ||||||
| chr3:168028601
|
T | C | 1 | a0001c0001t0002g0174 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1513+622A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168028601 | ||||||
| chr3:168028634
|
C | T | 6 | a0004c0004t0002g0139a0004c0004t0007g0141a0004c0004t0011g0193others(3): Show | 6 | HG02818.hp2 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1513+589G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168028634 | ||||||
| chr3:168028635
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1513+588C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 11/15 | chr3 | 168028635 | ||||||
| chr3:168029362
|
A | G | 1 | a0001c0001t0017g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1434-60T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 10/15 | chr3 | 168029362 | ||||||
| chr3:168029451
|
T | C | 9 | a0004c0004t0002g0139a0004c0004t0007g0141a0004c0004t0011g0193others(6): Show | 9 | HG01123.hp2 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.1434-149A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 10/15 | chr3 | 168029451 | ||||||
| chr3:168029591
|
C | G | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1433+189G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 10/15 | chr3 | 168029591 | ||||||
| chr3:168029615
|
A | G | 1 | a0002c0002t0008g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1433+165T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 10/15 | chr3 | 168029615 | ||||||
| chr3:168030041
|
G | A | 5 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1177-5C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030041 | ||||||
| chr3:168030138
|
T | C | 2 | a0001c0001t0002g0027a0001c0001t0002g0116 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1177-102A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030138 | ||||||
| chr3:168030161
|
C | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(27): Show | 31 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1177-125G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030161 | ||||||
| chr3:168030192
|
A | G | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1177-156T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030192 | ||||||
| chr3:168030268
|
T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1177-232A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030268 | ||||||
| chr3:168030510
|
C | CA | 7 | a0001c0001t0001g0172a0001c0001t0002g0027a0001c0001t0002g0116others(4): Show | 7 | HG01071.hp1 HG01361.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1177-475dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030510 | ||||||
| chr3:168030510
|
CA | C | 48 | a0001c0001t0002g0159a0001c0001t0003g0128a0001c0001t0004g0090others(45): Show | 48 | HG01081.hp1 HG01123.hp2 HG01169.hp1 others(45): Show |
intron_variant | MODIFIER | c.1177-475delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030510 | ||||||
| chr3:168030510
|
CAA | C | 57 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(54): Show | 58 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.1177-476_1177-475d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030510 | ||||||
| chr3:168030678
|
C | A | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1177-642G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030678 | ||||||
| chr3:168030704
|
G | T | 2 | a0001c0001t0012g0008a0001c0001t0012g0009 | 2 | HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1177-668C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030704 | ||||||
| chr3:168030822
|
A | C | 1 | a0002c0002t0005g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1177-786T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030822 | ||||||
| chr3:168030928
|
T | C | 1 | a0001c0001t0015g0033 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1177-892A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030928 | ||||||
| chr3:168030931
|
C | T | 5 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177-895G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030931 | ||||||
| chr3:168030948
|
A | G | 1 | a0001c0001t0002g0095 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1177-912T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030948 | ||||||
| chr3:168030999
|
G | A | 7 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1177-963C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168030999 | ||||||
| chr3:168031067
|
C | T | 2 | a0003c0003t0005g0197a0003c0003t0005g0198 | 2 | HG03491.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1177-1031G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031067 | ||||||
| chr3:168031109
|
A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1177-1073T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031109 | ||||||
| chr3:168031242
|
G | A | 1 | a0001c0001t0030g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1177-1206C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031242 | ||||||
| chr3:168031453
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1176+1067G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031453 | ||||||
| chr3:168031467
|
A | G | 6 | a0001c0001t0001g0087a0001c0001t0001g0152a0001c0001t0001g0177others(3): Show | 6 | HG00738.hp1 HG01069.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1176+1053T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031467 | ||||||
| chr3:168031518
|
T | C | 15 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(12): Show | 15 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1176+1002A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031518 | ||||||
| chr3:168031604
|
G | C | 4 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0039g0215others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1176+916C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031604 | ||||||
| chr3:168031662
|
G | C | 15 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(12): Show | 15 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1176+858C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031662 | ||||||
| chr3:168031664
|
T | C | 1 | a0001c0001t0001g0172 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1176+856A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031664 | ||||||
| chr3:168031727
|
G | A | 115 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0026others(112): Show | 115 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1176+793C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031727 | ||||||
| chr3:168031755
|
G | A | 21 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(18): Show | 21 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.1176+765C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031755 | ||||||
| chr3:168031827
|
C | A | 122 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(119): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1176+693G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031827 | ||||||
| chr3:168031867
|
TA | T | 3 | a0001c0001t0003g0080a0001c0001t0003g0113a0001c0001t0003g0114 | 3 | HG01071.hp1 HG01167.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1176+652delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031867 | ||||||
| chr3:168031964
|
C | G | 1 | a0002c0002t0008g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1176+556G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168031964 | ||||||
| chr3:168032155
|
T | C | 12 | a0001c0001t0002g0027a0001c0001t0002g0116a0001c0001t0008g0125others(9): Show | 12 | HG02071.hp1 HG02523.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1176+365A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168032155 | ||||||
| chr3:168032173
|
TG | T | 2 | a0001c0001t0001g0049a0001c0001t0034g0205 | 2 | HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1176+346delC | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 9/15 | chr3 | 168032173 | ||||||
| chr3:168033344
|
G | T | 1 | a0001c0008t0001g0015 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.844-492C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033344 | ||||||
| chr3:168033377
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.844-525C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033377 | ||||||
| chr3:168033441
|
TA | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(119): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.844-590delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033441 | ||||||
| chr3:168033456
|
A | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.844-604T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033456 | ||||||
| chr3:168033464
|
G | A | 2 | a0004c0004t0011g0193a0004c0004t0043g0225 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.844-612C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033464 | ||||||
| chr3:168033517
|
G | A | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.844-665C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033517 | ||||||
| chr3:168033606
|
C | CA | 48 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0049others(45): Show | 48 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.844-755dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
C | CAA | 26 | a0001c0001t0001g0053a0001c0001t0001g0148a0001c0001t0001g0149others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.844-756_844-755dup others(2): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
C | CAAA | 9 | a0001c0001t0001g0050a0001c0001t0002g0159a0001c0001t0003g0175others(6): Show | 9 | HG00140.hp2 HG01169.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-757_844-755dup others(3): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
C | CAAAA | 6 | a0001c0001t0006g0112a0001c0001t0007g0160a0001c0001t0011g0085others(3): Show | 6 | HG01175.hp1 HG01884.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-758_844-755dup others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
CA | C | 11 | a0001c0001t0004g0030a0001c0001t0007g0037a0001c0001t0007g0084others(8): Show | 11 | HG01346.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.844-755delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
CAA | C | 9 | a0001c0001t0002g0208a0001c0001t0007g0131a0001c0001t0012g0005others(6): Show | 9 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.844-756_844-755del others(2): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
CAAAA | C | 12 | a0001c0001t0001g0065a0001c0001t0002g0120a0001c0001t0004g0063others(9): Show | 12 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.844-758_844-755del others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
CAAAAA | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(47): Show | 51 | HG00280.hp1 HG01069.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.844-759_844-755del others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
CAAAAAA | C | 7 | a0001c0001t0001g0061a0001c0001t0001g0066a0001c0001t0001g0194others(4): Show | 7 | HG00099.hp1 HG00323.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-760_844-755del others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0022g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.844-768_844-755del others(14): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033606
|
CAAAAAAA others(15): Show |
C | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.844-776_844-755del others(22): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033606 | ||||||
| chr3:168033642
|
G | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.844-790C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033642 | ||||||
| chr3:168033647
|
C | T | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.844-795G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033647 | ||||||
| chr3:168033815
|
G | T | 36 | a0001c0001t0002g0027a0001c0001t0002g0116a0001c0001t0002g0136others(33): Show | 36 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.844-963C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033815 | ||||||
| chr3:168033851
|
C | T | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.844-999G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033851 | ||||||
| chr3:168033881
|
G | A | 39 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(36): Show | 40 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.844-1029C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033881 | ||||||
| chr3:168033975
|
C | G | 1 | a0001c0001t0003g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.844-1123G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033975 | ||||||
| chr3:168033998
|
G | GGTTA | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.844-1150_844-1147d others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168033998 | ||||||
| chr3:168034156
|
C | T | 1 | a0001c0001t0003g0165 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.844-1304G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168034156 | ||||||
| chr3:168034415
|
T | C | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.844-1563A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168034415 | ||||||
| chr3:168034416
|
G | A | 2 | a0001c0001t0021g0218a0001c0001t0040g0219 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.844-1564C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168034416 | ||||||
| chr3:168034445
|
G | A | 16 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.844-1593C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168034445 | ||||||
| chr3:168034707
|
T | C | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.844-1855A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168034707 | ||||||
| chr3:168034754
|
T | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.844-1902A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168034754 | ||||||
| chr3:168034937
|
A | G | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.843+1899T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168034937 | ||||||
| chr3:168034950
|
C | G | 6 | a0001c0001t0005g0201a0001c0001t0008g0101a0001c0001t0008g0195others(3): Show | 7 | HG02451.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+1886G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168034950 | ||||||
| chr3:168035021
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.843+1815C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035021 | ||||||
| chr3:168035037
|
C | CA | 5 | a0001c0001t0001g0045a0001c0001t0003g0041a0001c0001t0007g0084others(2): Show | 5 | HG00735.hp1 HG01243.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+1798dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035037 | ||||||
| chr3:168035037
|
CA | C | 12 | a0001c0001t0002g0027a0001c0001t0002g0116a0001c0001t0004g0090others(9): Show | 12 | HG01081.hp1 HG02071.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.843+1798delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035037 | ||||||
| chr3:168035037
|
CAA | C | 23 | a0001c0001t0002g0136a0001c0001t0002g0159a0001c0001t0002g0196others(20): Show | 23 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.843+1797_843+1798d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035037 | ||||||
| chr3:168035133
|
A | G | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.843+1703T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035133 | ||||||
| chr3:168035162
|
T | C | 1 | a0001c0001t0006g0086 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.843+1674A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035162 | ||||||
| chr3:168035614
|
T | C | 1 | a0001c0001t0009g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.843+1222A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035614 | ||||||
| chr3:168035782
|
A | G | 2 | a0002c0002t0008g0121a0002c0002t0022g0221 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.843+1054T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035782 | ||||||
| chr3:168035850
|
G | GA | 14 | a0001c0001t0002g0027a0001c0001t0002g0116a0001c0001t0003g0054others(11): Show | 14 | HG02071.hp1 HG02523.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.843+985dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035850 | ||||||
| chr3:168035913
|
TATG | T | 4 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0039g0215others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+920_843+922del others(3): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035913 | ||||||
| chr3:168035960
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.843+876T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168035960 | ||||||
| chr3:168036014
|
T | C | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.843+822A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036014 | ||||||
| chr3:168036126
|
T | C | 1 | a0002c0002t0002g0209 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.843+710A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036126 | ||||||
| chr3:168036132
|
G | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(119): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.843+704C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036132 | ||||||
| chr3:168036145
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.843+691G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036145 | ||||||
| chr3:168036312
|
G | A | 4 | a0001c0001t0008g0101a0001c0001t0008g0195a0001c0001t0018g0001others(1): Show | 5 | HG02451.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.843+524C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036312 | ||||||
| chr3:168036409
|
C | T | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.843+427G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036409 | ||||||
| chr3:168036414
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.843+422C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036414 | ||||||
| chr3:168036466
|
C | T | 4 | a0001c0001t0001g0047a0001c0001t0006g0086a0001c0001t0006g0146others(1): Show | 4 | HG01257.hp2 HG01346.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+370G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036466 | ||||||
| chr3:168036529
|
AT | A | 4 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0039g0215others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+306delA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036529 | ||||||
| chr3:168036785
|
A | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(119): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.843+51T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036785 | ||||||
| chr3:168036827
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.843+9C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 8/15 | chr3 | 168036827 | ||||||
| chr3:168037064
|
A | ATCTATGA others(26): Show |
38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(35): Show | 39 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.685-71_685-70insAC others(31): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037064 | ||||||
| chr3:168037085
|
A | G | 3 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0019g0079 | 3 | HG01243.hp2 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.685-91T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037085 | ||||||
| chr3:168037213
|
T | C | 1 | a0001c0001t0004g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.685-219A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037213 | ||||||
| chr3:168037318
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.685-324T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037318 | ||||||
| chr3:168037392
|
C | A | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.685-398G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037392 | ||||||
| chr3:168037451
|
T | TAC | 64 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0001g0162others(61): Show | 64 | HG00140.hp1 HG00558.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.685-459_685-458dup others(2): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037451 | ||||||
| chr3:168037451
|
T | TACAC | 18 | a0001c0001t0001g0148a0001c0001t0001g0183a0001c0001t0002g0136others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.685-461_685-458dup others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037451 | ||||||
| chr3:168037451
|
T | TACACAC | 7 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0013g0072others(4): Show | 7 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-463_685-458dup others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037451 | ||||||
| chr3:168037472
|
A | AC | 2 | a0001c0001t0001g0094a0001c0001t0011g0021 | 2 | HG02683.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.685-479_685-478ins others(1): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037472 | ||||||
| chr3:168037747
|
T | C | 9 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(6): Show | 9 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-753A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037747 | ||||||
| chr3:168037825
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0003g0076 | 2 | NA19012.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.685-831C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037825 | ||||||
| chr3:168037923
|
T | C | 35 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(32): Show | 36 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.685-929A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037923 | ||||||
| chr3:168037960
|
C | T | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.685-966G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037960 | ||||||
| chr3:168037961
|
G | A | 36 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(33): Show | 37 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.685-967C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037961 | ||||||
| chr3:168037975
|
G | A | 30 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0136others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.685-981C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168037975 | ||||||
| chr3:168038336
|
T | C | 1 | a0001c0001t0009g0134 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.685-1342A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168038336 | ||||||
| chr3:168038449
|
G | A | 5 | a0001c0001t0004g0071a0001c0001t0004g0155a0001c0001t0004g0158others(2): Show | 5 | HG02040.hp1 NA18960.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-1455C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168038449 | ||||||
| chr3:168038619
|
C | A | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.685-1625G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168038619 | ||||||
| chr3:168039075
|
T | C | 4 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+1711A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039075 | ||||||
| chr3:168039264
|
A | AT | 23 | a0001c0001t0002g0027a0001c0001t0002g0116a0001c0001t0002g0208others(20): Show | 23 | HG00140.hp1 HG01175.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.684+1521dupA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039264 | ||||||
| chr3:168039264
|
A | T | 3 | a0001c0001t0004g0031a0001c0001t0008g0098a0004c0004t0038g0214 | 3 | HG00738.hp2 HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.684+1522T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039264 | ||||||
| chr3:168039264
|
AT | A | 13 | a0001c0001t0001g0053a0001c0001t0002g0136a0001c0001t0002g0196others(10): Show | 13 | HG02071.hp1 HG02523.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.684+1521delA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039264 | ||||||
| chr3:168039264
|
ATT | A | 16 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.684+1520_684+1521d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039264 | ||||||
| chr3:168039271
|
T | G | 7 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(4): Show | 7 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.684+1515A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039271 | ||||||
| chr3:168039312
|
G | T | 2 | a0001c0001t0003g0041a0001c0001t0003g0044 | 2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.684+1474C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039312 | ||||||
| chr3:168039424
|
T | C | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.684+1362A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039424 | ||||||
| chr3:168039557
|
C | T | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.684+1229G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039557 | ||||||
| chr3:168039718
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.684+1068T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039718 | ||||||
| chr3:168039831
|
A | C | 39 | a0001c0001t0002g0136a0001c0001t0002g0159a0001c0001t0002g0196others(36): Show | 39 | HG00140.hp1 HG00738.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.684+955T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039831 | ||||||
| chr3:168039899
|
A | T | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.684+887T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039899 | ||||||
| chr3:168039968
|
A | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0116 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.684+818T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039968 | ||||||
| chr3:168039992
|
A | G | 1 | a0003c0003t0005g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.684+794T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168039992 | ||||||
| chr3:168040261
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.684+525C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168040261 | ||||||
| chr3:168040411
|
G | A | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.684+375C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168040411 | ||||||
| chr3:168040457
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.684+329G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168040457 | ||||||
| chr3:168040464
|
A | G | 1 | a0001c0001t0019g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.684+322T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168040464 | ||||||
| chr3:168040509
|
C | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.684+277G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168040509 | ||||||
| chr3:168040708
|
G | A | 6 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(3): Show | 6 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.684+78C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168040708 | ||||||
| chr3:168040717
|
T | C | 1 | a0001c0001t0034g0205 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.684+69A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 7/15 | chr3 | 168040717 | ||||||
| chr3:168040896
|
G | A | 1 | a0001c0001t0007g0160 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.601-27C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 6/15 | chr3 | 168040896 | ||||||
| chr3:168041148
|
G | T | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.600+244C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 6/15 | chr3 | 168041148 | ||||||
| chr3:168041168
|
C | T | 24 | a0001c0001t0002g0136a0001c0001t0002g0159a0001c0001t0002g0196others(21): Show | 24 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.600+224G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 6/15 | chr3 | 168041168 | ||||||
| chr3:168041176
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(35): Show | 39 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.600+216A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 6/15 | chr3 | 168041176 | ||||||
| chr3:168041573
|
A | T | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.518-99T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168041573 | ||||||
| chr3:168041779
|
C | A | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.518-305G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168041779 | ||||||
| chr3:168041957
|
CTATT | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.518-487_518-484del others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168041957 | ||||||
| chr3:168042017
|
G | C | 2 | a0001c0001t0021g0218a0001c0001t0040g0219 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.518-543C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042017 | ||||||
| chr3:168042239
|
C | T | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.518-765G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042239 | ||||||
| chr3:168042386
|
G | T | 35 | a0001c0001t0002g0027a0001c0001t0002g0116a0001c0001t0002g0136others(32): Show | 35 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.518-912C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042386 | ||||||
| chr3:168042434
|
C | T | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517+945G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042434 | ||||||
| chr3:168042435
|
G | A | 30 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0136others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.517+944C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042435 | ||||||
| chr3:168042454
|
T | C | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517+925A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042454 | ||||||
| chr3:168042547
|
C | T | 1 | a0001c0001t0016g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.517+832G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042547 | ||||||
| chr3:168042577
|
G | A | 1 | a0001c0001t0018g0001 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.517+802C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042577 | ||||||
| chr3:168042776
|
T | C | 11 | a0001c0001t0002g0027a0001c0001t0002g0116a0003c0003t0005g0145others(8): Show | 11 | HG02071.hp1 HG02523.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+603A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042776 | ||||||
| chr3:168042831
|
A | G | 9 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0090others(6): Show | 9 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+548T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042831 | ||||||
| chr3:168042861
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.517+518A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042861 | ||||||
| chr3:168042974
|
G | C | 1 | a0003c0003t0013g0150 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.517+405C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168042974 | ||||||
| chr3:168043025
|
T | C | 1 | a0001c0001t0002g0174 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.517+354A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168043025 | ||||||
| chr3:168043178
|
C | T | 1 | a0002c0002t0008g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517+201G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168043178 | ||||||
| chr3:168043185
|
T | C | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.517+194A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168043185 | ||||||
| chr3:168043282
|
A | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.517+97T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168043282 | ||||||
| chr3:168043282
|
A | T | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.517+97T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 5/15 | chr3 | 168043282 | ||||||
| chr3:168043731
|
C | T | 16 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.367-202G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 4/15 | chr3 | 168043731 | ||||||
| chr3:168043924
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.367-395G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 4/15 | chr3 | 168043924 | ||||||
| chr3:168044000
|
T | A | 11 | a0001c0001t0002g0027a0001c0001t0002g0116a0003c0003t0005g0145others(8): Show | 11 | HG02071.hp1 HG02523.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.367-471A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 4/15 | chr3 | 168044000 | ||||||
| chr3:168044051
|
T | C | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.367-522A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 4/15 | chr3 | 168044051 | ||||||
| chr3:168044258
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(97): Show | 101 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.366+570G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 4/15 | chr3 | 168044258 | ||||||
| chr3:168044259
|
G | C | 1 | a0001c0001t0003g0175 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.366+569C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 4/15 | chr3 | 168044259 | ||||||
| chr3:168044310
|
T | C | 4 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0039g0215others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+518A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 4/15 | chr3 | 168044310 | ||||||
| chr3:168044348
|
G | C | 57 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0116others(54): Show | 57 | HG00140.hp1 HG00738.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.366+480C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 4/15 | chr3 | 168044348 | ||||||
| chr3:168044385
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.366+443A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 4/15 | chr3 | 168044385 | ||||||
| chr3:168044890
|
C | CA | 88 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.313-10dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168044890 | ||||||
| chr3:168044890
|
CA | C | 9 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(6): Show | 9 | HG01081.hp2 HG02109.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.313-10delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168044890 | ||||||
| chr3:168044979
|
C | T | 1 | a0002c0002t0026g0110 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.313-98G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168044979 | ||||||
| chr3:168045231
|
A | G | 1 | a0001c0001t0010g0023 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.313-350T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045231 | ||||||
| chr3:168045232
|
T | C | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.313-351A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045232 | ||||||
| chr3:168045274
|
C | T | 16 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.313-393G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045274 | ||||||
| chr3:168045507
|
C | T | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.313-626G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045507 | ||||||
| chr3:168045508
|
G | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.313-627C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045508 | ||||||
| chr3:168045681
|
C | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0095 | 2 | HG00280.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.313-800G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045681 | ||||||
| chr3:168045683
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.313-802A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045683 | ||||||
| chr3:168045728
|
T | C | 23 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(20): Show | 23 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.313-847A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045728 | ||||||
| chr3:168045730
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.313-849T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045730 | ||||||
| chr3:168045808
|
C | G | 1 | a0001c0001t0001g0194 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.313-927G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168045808 | ||||||
| chr3:168046108
|
G | C | 2 | a0002c0002t0005g0104a0002c0002t0013g0108 | 2 | HG01243.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.312+842C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046108 | ||||||
| chr3:168046248
|
G | T | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.312+702C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046248 | ||||||
| chr3:168046520
|
C | T | 23 | a0001c0001t0002g0208a0001c0001t0004g0028a0001c0001t0004g0030others(20): Show | 23 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.312+430G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046520 | ||||||
| chr3:168046565
|
C | A | 1 | a0001c0001t0004g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.312+385G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046565 | ||||||
| chr3:168046584
|
T | C | 2 | a0001c0001t0016g0004a0001c0001t0019g0119 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.312+366A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046584 | ||||||
| chr3:168046658
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0173 | 2 | HG00140.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.312+292G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046658 | ||||||
| chr3:168046806
|
C | CA | 26 | a0001c0001t0006g0169a0001c0001t0016g0003a0002c0002t0002g0109others(23): Show | 26 | HG01243.hp1 HG02055.hp1 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.312+143dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046806 | ||||||
| chr3:168046806
|
C | CAA | 21 | a0001c0001t0002g0208a0001c0001t0004g0028a0001c0001t0004g0030others(18): Show | 21 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.312+142_312+143dup others(2): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046806 | ||||||
| chr3:168046806
|
CA | C | 12 | a0001c0001t0002g0095a0001c0001t0002g0159a0001c0001t0005g0137others(9): Show | 12 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.312+143delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046806 | ||||||
| chr3:168046824
|
G | T | 1 | a0001c0001t0017g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.312+126C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046824 | ||||||
| chr3:168046877
|
TTC | T | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.312+71_312+72delGA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046877 | ||||||
| chr3:168046931
|
C | CA | 6 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(3): Show | 6 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.312+18dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 3/15 | chr3 | 168046931 | ||||||
| chr3:168047032
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(36): Show | 40 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.263-33T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 2/15 | chr3 | 168047032 | ||||||
| chr3:168047341
|
A | G | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.263-342T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 2/15 | chr3 | 168047341 | ||||||
| chr3:168047569
|
C | T | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.263-570G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 2/15 | chr3 | 168047569 | ||||||
| chr3:168047708
|
C | T | 23 | a0001c0001t0002g0208a0001c0001t0004g0028a0001c0001t0004g0030others(20): Show | 23 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.262+583G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 2/15 | chr3 | 168047708 | ||||||
| chr3:168047874
|
G | C | 7 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(4): Show | 7 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.262+417C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 2/15 | chr3 | 168047874 | ||||||
| chr3:168048048
|
G | A | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.262+243C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 2/15 | chr3 | 168048048 | ||||||
| chr3:168048082
|
A | T | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.262+209T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 2/15 | chr3 | 168048082 | ||||||
| chr3:168048162
|
C | T | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.262+129G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 2/15 | chr3 | 168048162 | ||||||
| chr3:168048197
|
C | T | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.262+94G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 2/15 | chr3 | 168048197 | ||||||
| chr3:168048409
|
TTAAAAC | T | 23 | a0001c0001t0002g0136a0001c0001t0002g0159a0001c0001t0002g0196others(20): Show | 23 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.188-50_188-45delGT others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168048409 | ||||||
| chr3:168048639
|
T | C | 5 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-274A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168048639 | ||||||
| chr3:168048703
|
C | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.188-338G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168048703 | ||||||
| chr3:168048735
|
C | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-370G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168048735 | ||||||
| chr3:168048745
|
T | C | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.188-380A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168048745 | ||||||
| chr3:168048893
|
A | G | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.188-528T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168048893 | ||||||
| chr3:168048946
|
G | A | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.188-581C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168048946 | ||||||
| chr3:168048960
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.188-595T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168048960 | ||||||
| chr3:168049259
|
C | G | 1 | a0001c0001t0003g0055 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.188-894G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049259 | ||||||
| chr3:168049452
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.188-1087G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049452 | ||||||
| chr3:168049453
|
C | T | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-1088G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049453 | ||||||
| chr3:168049454
|
G | T | 1 | a0001c0001t0002g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.188-1089C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049454 | ||||||
| chr3:168049459
|
A | AGAG | 109 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.188-1097_188-1095d others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049459 | ||||||
| chr3:168049490
|
C | T | 1 | a0001c0001t0004g0155 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.188-1125G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049490 | ||||||
| chr3:168049590
|
C | T | 23 | a0001c0001t0002g0136a0001c0001t0002g0159a0001c0001t0002g0196others(20): Show | 23 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.188-1225G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049590 | ||||||
| chr3:168049772
|
A | G | 1 | a0002c0002t0022g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.188-1407T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049772 | ||||||
| chr3:168049863
|
T | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.188-1498A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049863 | ||||||
| chr3:168049892
|
T | A | 1 | a0001c0001t0009g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.188-1527A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168049892 | ||||||
| chr3:168050238
|
A | C | 1 | a0002c0002t0005g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.188-1873T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050238 | ||||||
| chr3:168050261
|
T | TA | 46 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0136others(43): Show | 46 | HG00140.hp1 HG00738.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.188-1897dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050261 | ||||||
| chr3:168050369
|
C | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0116 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.188-2004G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050369 | ||||||
| chr3:168050397
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0011g0021 | 2 | HG02683.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.188-2032T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050397 | ||||||
| chr3:168050429
|
T | C | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.188-2064A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050429 | ||||||
| chr3:168050533
|
A | G | 4 | a0001c0001t0008g0101a0001c0001t0008g0195a0001c0001t0018g0001others(1): Show | 5 | HG02451.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-2168T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050533 | ||||||
| chr3:168050570
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-2205G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050570 | ||||||
| chr3:168050698
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.188-2333T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050698 | ||||||
| chr3:168050822
|
T | TATA | 38 | a0001c0001t0001g0049a0001c0001t0001g0149a0001c0001t0001g0179others(35): Show | 39 | HG00558.hp1 HG00738.hp2 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.188-2460_188-2458d others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050822
|
T | TATAATA | 22 | a0001c0001t0001g0050a0001c0001t0001g0152a0001c0001t0001g0167others(19): Show | 22 | HG00140.hp2 HG00642.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.188-2463_188-2458d others(8): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050822
|
T | TATAATAA others(2): Show |
12 | a0001c0001t0006g0147a0001c0001t0007g0036a0001c0001t0007g0132others(9): Show | 12 | HG01255.hp2 HG01257.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.188-2466_188-2458d others(11): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050822
|
T | TATAATAA others(5): Show |
5 | a0001c0001t0001g0184a0001c0001t0006g0048a0003c0003t0013g0072others(2): Show | 5 | NA18945.hp2 NA18977.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-2469_188-2458d others(14): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050822
|
TATA | T | 18 | a0001c0001t0001g0058a0001c0001t0001g0162a0001c0001t0002g0027others(15): Show | 18 | HG01069.hp2 HG01106.hp2 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.188-2460_188-2458d others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050822
|
TATAATA | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0053a0001c0001t0001g0161others(7): Show | 10 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-2463_188-2458d others(8): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050822
|
TATAATAA others(2): Show |
T | 6 | a0001c0001t0003g0175a0001c0001t0010g0016a0001c0001t0010g0023others(3): Show | 6 | HG01169.hp2 HG01516.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-2466_188-2458d others(11): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050822
|
TATAATAA others(5): Show |
T | 18 | a0001c0001t0002g0208a0001c0001t0003g0022a0001c0001t0003g0054others(15): Show | 18 | HG02109.hp1 HG02109.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.188-2469_188-2458d others(14): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050822
|
TATAATAA others(8): Show |
T | 3 | a0001c0001t0002g0100a0001c0001t0004g0068a0001c0001t0004g0206 | 3 | HG02886.hp2 HG04228.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.188-2472_188-2458d others(17): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050822
|
TATAATAA others(11): Show |
T | 35 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(32): Show | 36 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.188-2475_188-2458d others(20): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050822 | ||||||
| chr3:168050860
|
T | A | 1 | a0001c0001t0030g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.188-2495A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050860 | ||||||
| chr3:168050860
|
T | TAATAAA | 2 | a0001c0001t0019g0079a0001c0001t0023g0010 | 2 | HG02145.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.188-2496_188-2495i others(8): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050860 | ||||||
| chr3:168050860
|
T | TAATAATA others(2): Show |
3 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126 | 3 | HG01243.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.188-2496_188-2495i others(11): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050860 | ||||||
| chr3:168050860
|
T | TAATAATA others(5): Show |
1 | a0001c0001t0037g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.188-2507_188-2496d others(14): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050860 | ||||||
| chr3:168050938
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-2573C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168050938 | ||||||
| chr3:168051052
|
G | A | 38 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(35): Show | 38 | HG00140.hp1 HG00738.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.188-2687C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051052 | ||||||
| chr3:168051101
|
G | C | 1 | a0001c0001t0005g0137 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.188-2736C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051101 | ||||||
| chr3:168051134
|
A | G | 1 | a0001c0001t0014g0117 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.188-2769T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051134 | ||||||
| chr3:168051227
|
T | C | 5 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0014g0102others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-2862A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051227 | ||||||
| chr3:168051291
|
AC | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.188-2927delG | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051291 | ||||||
| chr3:168051431
|
G | A | 1 | a0002c0002t0022g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.188-3066C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051431 | ||||||
| chr3:168051585
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.188-3220C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051585 | ||||||
| chr3:168051712
|
G | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-3347C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051712 | ||||||
| chr3:168051769
|
G | A | 5 | a0001c0001t0001g0148a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG00558.hp2 HG02559.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-3404C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051769 | ||||||
| chr3:168051830
|
G | A | 2 | a0001c0001t0021g0218a0001c0001t0040g0219 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.188-3465C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051830 | ||||||
| chr3:168051874
|
A | G | 6 | a0001c0001t0005g0201a0001c0001t0008g0101a0001c0001t0008g0195others(3): Show | 7 | HG02451.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-3509T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051874 | ||||||
| chr3:168051879
|
T | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-3514A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051879 | ||||||
| chr3:168051930
|
T | TCA | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.188-3567_188-3566d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168051930 | ||||||
| chr3:168052005
|
G | T | 15 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-3640C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052005 | ||||||
| chr3:168052033
|
A | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.188-3668T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052033 | ||||||
| chr3:168052039
|
C | T | 4 | a0001c0001t0002g0159a0001c0001t0014g0096a0001c0001t0014g0143others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-3674G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052039 | ||||||
| chr3:168052040
|
C | T | 19 | a0001c0001t0002g0159a0001c0001t0005g0115a0001c0001t0005g0137others(16): Show | 19 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-3675G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052040 | ||||||
| chr3:168052118
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-3753A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052118 | ||||||
| chr3:168052327
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.188-3962G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052327 | ||||||
| chr3:168052336
|
G | A | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.188-3971C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052336 | ||||||
| chr3:168052355
|
CAT | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(74): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.188-3992_188-3991d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052355 | ||||||
| chr3:168052369
|
T | C | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.188-4004A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052369 | ||||||
| chr3:168052398
|
ACT | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-4035_188-4034d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052398 | ||||||
| chr3:168052406
|
T | A | 5 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0014g0102others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-4041A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052406 | ||||||
| chr3:168052423
|
TAC | T | 2 | a0001c0001t0001g0053a0001c0001t0009g0052 | 2 | NA18945.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.188-4060_188-4059d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052423 | ||||||
| chr3:168052497
|
A | G | 1 | a0001c0001t0014g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-4132T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052497 | ||||||
| chr3:168052512
|
AAAT | A | 7 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-4150_188-4148d others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052512 | ||||||
| chr3:168052563
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0009g0077a0005c0006t0008g0133 | 3 | HG01123.hp2 NA19074.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.188-4198G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052563 | ||||||
| chr3:168052686
|
G | A | 18 | a0001c0001t0002g0138a0001c0001t0005g0201a0001c0001t0007g0036others(15): Show | 19 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-4321C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052686 | ||||||
| chr3:168052850
|
T | C | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-4485A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052850 | ||||||
| chr3:168052938
|
T | C | 1 | a0001c0001t0003g0154 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.188-4573A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168052938 | ||||||
| chr3:168053082
|
A | T | 2 | a0001c0001t0002g0027a0001c0001t0002g0116 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.188-4717T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053082 | ||||||
| chr3:168053122
|
C | T | 2 | a0002c0002t0005g0140a0002c0002t0005g0212 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.188-4757G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053122 | ||||||
| chr3:168053140
|
C | T | 1 | a0002c0002t0022g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.188-4775G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053140 | ||||||
| chr3:168053213
|
A | C | 1 | a0001c0001t0002g0174 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.188-4848T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053213 | ||||||
| chr3:168053353
|
G | A | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.188-4988C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053353 | ||||||
| chr3:168053374
|
C | T | 2 | a0001c0001t0003g0175a0001c0001t0003g0200 | 2 | NA18994.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.188-5009G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053374 | ||||||
| chr3:168053600
|
G | A | 5 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0014g0102others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-5235C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053600 | ||||||
| chr3:168053740
|
C | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.188-5375G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053740 | ||||||
| chr3:168053767
|
T | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.188-5402A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053767 | ||||||
| chr3:168053836
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(36): Show | 40 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.188-5471A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053836 | ||||||
| chr3:168053869
|
G | A | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.188-5504C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053869 | ||||||
| chr3:168053892
|
T | G | 1 | a0001c0009t0004g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.188-5527A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053892 | ||||||
| chr3:168053905
|
T | G | 14 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(11): Show | 14 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.188-5540A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168053905 | ||||||
| chr3:168054061
|
T | C | 7 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(4): Show | 7 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-5696A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054061 | ||||||
| chr3:168054076
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-5711A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054076 | ||||||
| chr3:168054104
|
C | G | 5 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-5739G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054104 | ||||||
| chr3:168054227
|
T | C | 2 | a0001c0001t0016g0003a0002c0002t0005g0105 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.188-5862A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054227 | ||||||
| chr3:168054243
|
G | C | 5 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0014g0102others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-5878C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054243 | ||||||
| chr3:168054292
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(36): Show | 40 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.188-5927G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054292 | ||||||
| chr3:168054307
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.188-5942T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054307 | ||||||
| chr3:168054516
|
T | C | 5 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0014g0102others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-6151A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054516 | ||||||
| chr3:168054633
|
AAAT | A | 15 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-6271_188-6269d others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054633 | ||||||
| chr3:168054650
|
ACT | A | 6 | a0001c0001t0005g0201a0001c0001t0008g0101a0001c0001t0008g0195others(3): Show | 7 | HG02451.hp1 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-6287_188-6286d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054650 | ||||||
| chr3:168054721
|
G | A | 1 | a0002c0002t0022g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.188-6356C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054721 | ||||||
| chr3:168054762
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-6397C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054762 | ||||||
| chr3:168054831
|
G | A | 8 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-6466C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054831 | ||||||
| chr3:168054994
|
C | T | 5 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0014g0102others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-6629G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168054994 | ||||||
| chr3:168055203
|
T | C | 8 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-6838A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055203 | ||||||
| chr3:168055483
|
T | A | 10 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(7): Show | 10 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.188-7118A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055483 | ||||||
| chr3:168055498
|
C | A | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.188-7133G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055498 | ||||||
| chr3:168055650
|
AC | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-7286delG | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055650 | ||||||
| chr3:168055726
|
C | T | 5 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0014g0102others(2): Show | 5 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-7361G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055726 | ||||||
| chr3:168055727
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(105): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.188-7362T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055727 | ||||||
| chr3:168055781
|
G | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-7416C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055781 | ||||||
| chr3:168055799
|
C | G | 26 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(23): Show | 26 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.188-7434G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055799 | ||||||
| chr3:168055801
|
C | CA | 13 | a0001c0001t0002g0208a0001c0001t0006g0086a0001c0001t0008g0125others(10): Show | 13 | HG01123.hp2 HG01361.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.188-7437dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055801 | ||||||
| chr3:168055801
|
C | CAA | 56 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(53): Show | 57 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.188-7438_188-7437d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055801 | ||||||
| chr3:168055802
|
A | C | 5 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-7437T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055802 | ||||||
| chr3:168055981
|
A | T | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.188-7616T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055981 | ||||||
| chr3:168055991
|
A | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(68): Show | 72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.188-7626T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168055991 | ||||||
| chr3:168056165
|
T | G | 1 | a0001c0001t0014g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-7800A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168056165 | ||||||
| chr3:168056241
|
C | T | 13 | a0001c0001t0002g0159a0001c0001t0010g0016a0001c0001t0014g0096others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.188-7876G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168056241 | ||||||
| chr3:168056242
|
G | A | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.188-7877C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168056242 | ||||||
| chr3:168056565
|
C | G | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.188-8200G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168056565 | ||||||
| chr3:168056582
|
C | G | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.188-8217G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168056582 | ||||||
| chr3:168056679
|
T | G | 4 | a0001c0001t0008g0101a0001c0001t0008g0195a0001c0001t0018g0001others(1): Show | 5 | HG02451.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-8314A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168056679 | ||||||
| chr3:168056701
|
T | A | 2 | a0001c0001t0016g0004a0001c0001t0019g0119 | 2 | HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.188-8336A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168056701 | ||||||
| chr3:168056706
|
C | T | 1 | a0001c0001t0006g0017 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.188-8341G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168056706 | ||||||
| chr3:168056892
|
C | T | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.188-8527G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168056892 | ||||||
| chr3:168057230
|
C | T | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.188-8865G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168057230 | ||||||
| chr3:168057245
|
G | A | 8 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-8880C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168057245 | ||||||
| chr3:168057355
|
G | A | 2 | a0001c0001t0002g0027a0001c0001t0002g0116 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.188-8990C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168057355 | ||||||
| chr3:168057355
|
G | C | 1 | a0001c0001t0001g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.188-8990C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168057355 | ||||||
| chr3:168057405
|
G | A | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.188-9040C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168057405 | ||||||
| chr3:168057422
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.188-9057G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168057422 | ||||||
| chr3:168057627
|
C | T | 18 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(15): Show | 18 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.188-9262G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168057627 | ||||||
| chr3:168057803
|
C | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.188-9438G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168057803 | ||||||
| chr3:168057923
|
C | T | 3 | a0001c0001t0002g0078a0001c0001t0002g0095a0006c0007t0002g0046 | 3 | HG00280.hp2 HG01361.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.188-9558G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168057923 | ||||||
| chr3:168058141
|
G | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-9776C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168058141 | ||||||
| chr3:168058163
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-9798A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168058163 | ||||||
| chr3:168058176
|
A | C | 49 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(46): Show | 49 | HG00140.hp1 HG00738.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.188-9811T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168058176 | ||||||
| chr3:168058263
|
T | C | 1 | a0004c0004t0038g0214 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188-9898A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168058263 | ||||||
| chr3:168058348
|
A | G | 1 | a0002c0002t0005g0106 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.188-9983T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168058348 | ||||||
| chr3:168058577
|
A | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.188-10212T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168058577 | ||||||
| chr3:168058724
|
G | A | 1 | a0001c0001t0010g0059 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.188-10359C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168058724 | ||||||
| chr3:168058974
|
G | A | 16 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(13): Show | 16 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-10609C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168058974 | ||||||
| chr3:168059084
|
C | T | 56 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(53): Show | 57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.188-10719G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168059084 | ||||||
| chr3:168059352
|
C | T | 1 | a0001c0001t0037g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.188-10987G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168059352 | ||||||
| chr3:168059466
|
T | C | 56 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(53): Show | 57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.188-11101A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168059466 | ||||||
| chr3:168059850
|
A | G | 16 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(13): Show | 16 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-11485T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168059850 | ||||||
| chr3:168059967
|
T | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.188-11602A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168059967 | ||||||
| chr3:168059979
|
G | A | 4 | a0003c0003t0013g0072a0003c0003t0013g0150a0003c0003t0013g0199others(1): Show | 4 | NA18945.hp2 NA18977.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-11614C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168059979 | ||||||
| chr3:168060067
|
T | A | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.188-11702A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168060067 | ||||||
| chr3:168060100
|
G | GT | 83 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(80): Show | 84 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.188-11736dupA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168060100 | ||||||
| chr3:168060373
|
G | A | 17 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(14): Show | 17 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-12008C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168060373 | ||||||
| chr3:168060755
|
T | C | 1 | a0001c0008t0001g0015 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.188-12390A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168060755 | ||||||
| chr3:168060860
|
G | A | 1 | a0001c0001t0030g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.188-12495C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168060860 | ||||||
| chr3:168060938
|
ACTTTGTA others(1): Show |
A | 45 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.188-12581_188-1257 others(12): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168060938 | ||||||
| chr3:168060942
|
T | G | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.188-12577A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168060942 | ||||||
| chr3:168060947
|
G | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.188-12582C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168060947 | ||||||
| chr3:168061051
|
G | A | 13 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(10): Show | 13 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-12686C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168061051 | ||||||
| chr3:168061102
|
G | A | 7 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-12737C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168061102 | ||||||
| chr3:168061108
|
AT | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(83): Show | 87 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.188-12744delA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168061108 | ||||||
| chr3:168061145
|
C | CA | 36 | a0001c0001t0001g0042a0001c0001t0001g0166a0001c0001t0002g0034others(33): Show | 36 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.188-12781dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168061145 | ||||||
| chr3:168061145
|
CA | C | 7 | a0001c0001t0002g0100a0001c0001t0002g0174a0001c0001t0003g0019others(4): Show | 7 | HG01993.hp1 HG01993.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-12781delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168061145 | ||||||
| chr3:168061328
|
G | T | 1 | a0001c0001t0003g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.188-12963C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168061328 | ||||||
| chr3:168061356
|
T | G | 53 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.188-12991A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168061356 | ||||||
| chr3:168061679
|
G | C | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.188-13314C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168061679 | ||||||
| chr3:168061945
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-13580A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168061945 | ||||||
| chr3:168062013
|
T | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-13648A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168062013 | ||||||
| chr3:168062059
|
G | T | 1 | a0001c0001t0003g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.188-13694C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168062059 | ||||||
| chr3:168062263
|
C | G | 1 | a0001c0001t0007g0131 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.188-13898G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168062263 | ||||||
| chr3:168062401
|
C | CT | 18 | a0001c0001t0003g0081a0001c0001t0004g0028a0001c0001t0004g0030others(15): Show | 18 | HG00140.hp1 HG00738.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.188-14037dupA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168062401 | ||||||
| chr3:168062494
|
T | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-14129A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168062494 | ||||||
| chr3:168062549
|
A | G | 1 | a0001c0001t0004g0031 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.188-14184T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168062549 | ||||||
| chr3:168062592
|
C | T | 7 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(4): Show | 7 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-14227G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168062592 | ||||||
| chr3:168062738
|
C | T | 16 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(13): Show | 16 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-14373G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168062738 | ||||||
| chr3:168062749
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.188-14384A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168062749 | ||||||
| chr3:168063058
|
C | G | 1 | a0001c0001t0004g0135 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.188-14693G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063058 | ||||||
| chr3:168063398
|
T | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-15033A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063398 | ||||||
| chr3:168063423
|
G | A | 4 | a0001c0001t0001g0187a0001c0001t0001g0191a0001c0001t0002g0069others(1): Show | 4 | HG01261.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-15058C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063423 | ||||||
| chr3:168063484
|
A | C | 2 | a0001c0001t0002g0136a0001c0001t0014g0102 | 2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.188-15119T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063484 | ||||||
| chr3:168063594
|
T | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.188-15229A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063594 | ||||||
| chr3:168063700
|
C | T | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-15335G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063700 | ||||||
| chr3:168063835
|
T | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(41): Show | 45 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.188-15470A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063835 | ||||||
| chr3:168063885
|
G | GA | 6 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(3): Show | 6 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-15521dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063885 | ||||||
| chr3:168063899
|
C | T | 1 | a0001c0001t0014g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.188-15534G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063899 | ||||||
| chr3:168063959
|
T | C | 7 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(4): Show | 7 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-15594A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063959 | ||||||
| chr3:168063973
|
G | T | 1 | a0001c0001t0017g0122 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.188-15608C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168063973 | ||||||
| chr3:168064154
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.188-15789G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064154 | ||||||
| chr3:168064246
|
A | G | 33 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(30): Show | 33 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.188-15881T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064246 | ||||||
| chr3:168064247
|
C | T | 1 | a0002c0002t0008g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.188-15882G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064247 | ||||||
| chr3:168064292
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.188-15927T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064292 | ||||||
| chr3:168064350
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-15985T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064350 | ||||||
| chr3:168064533
|
T | C | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-16168A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064533 | ||||||
| chr3:168064535
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.188-16170C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064535 | ||||||
| chr3:168064548
|
T | G | 1 | a0001c0001t0001g0053 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.188-16183A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064548 | ||||||
| chr3:168064573
|
A | G | 34 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(31): Show | 34 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.188-16208T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064573 | ||||||
| chr3:168064602
|
A | AT | 27 | a0001c0001t0001g0203a0001c0001t0004g0028a0001c0001t0004g0030others(24): Show | 27 | HG00140.hp1 HG00738.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.188-16238dupA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064602 | ||||||
| chr3:168064602
|
A | ATT | 44 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(41): Show | 45 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.188-16239_188-1623 others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064602 | ||||||
| chr3:168064602
|
AT | A | 23 | a0001c0001t0002g0159a0001c0001t0003g0114a0001c0001t0005g0137others(20): Show | 23 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.188-16238delA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064602 | ||||||
| chr3:168064610
|
T | TG | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-16246_188-1624 others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064610 | ||||||
| chr3:168064724
|
A | ATGCC | 25 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(22): Show | 25 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.188-16363_188-1636 others(8): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064724 | ||||||
| chr3:168064862
|
T | G | 1 | a0002c0002t0005g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.188-16497A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064862 | ||||||
| chr3:168064901
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.188-16536A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064901 | ||||||
| chr3:168064957
|
A | AG | 7 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-16593dupC | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064957 | ||||||
| chr3:168064961
|
A | G | 43 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(40): Show | 43 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.188-16596T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168064961 | ||||||
| chr3:168065226
|
A | G | 15 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-16861T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168065226 | ||||||
| chr3:168065390
|
A | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(53): Show | 57 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.188-17025T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168065390 | ||||||
| chr3:168065519
|
G | A | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-17154C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168065519 | ||||||
| chr3:168065594
|
T | C | 4 | a0001c0001t0002g0100a0001c0001t0042g0222a0004c0004t0011g0193others(1): Show | 4 | HG02886.hp2 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-17229A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168065594 | ||||||
| chr3:168065596
|
G | C | 1 | a0001c0001t0010g0060 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.188-17231C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168065596 | ||||||
| chr3:168065825
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.188-17460C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168065825 | ||||||
| chr3:168065862
|
G | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-17497C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168065862 | ||||||
| chr3:168066178
|
C | CT | 19 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0148others(16): Show | 19 | HG00140.hp2 HG00280.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.188-17814dupA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168066178 | ||||||
| chr3:168066328
|
C | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(105): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.188-17963G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168066328 | ||||||
| chr3:168066363
|
T | C | 1 | a0001c0001t0006g0075 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.188-17998A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168066363 | ||||||
| chr3:168066717
|
G | A | 1 | a0001c0005t0001g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.188-18352C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168066717 | ||||||
| chr3:168066862
|
G | A | 1 | a0001c0001t0008g0099 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.188-18497C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168066862 | ||||||
| chr3:168066908
|
A | G | 1 | a0002c0002t0005g0103 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.188-18543T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168066908 | ||||||
| chr3:168066938
|
C | T | 121 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(118): Show | 122 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.188-18573G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168066938 | ||||||
| chr3:168067098
|
C | A | 1 | a0001c0001t0004g0030 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.188-18733G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067098 | ||||||
| chr3:168067180
|
A | G | 1 | a0004c0004t0011g0193 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-18815T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067180 | ||||||
| chr3:168067226
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.188-18861C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067226 | ||||||
| chr3:168067428
|
A | G | 1 | a0002c0002t0022g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.188-19063T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067428 | ||||||
| chr3:168067523
|
A | AC | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-19159_188-1915 others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067523 | ||||||
| chr3:168067525
|
A | AC | 9 | a0001c0001t0001g0014a0001c0001t0008g0195a0001c0001t0016g0004others(6): Show | 9 | HG02055.hp2 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-19161_188-1916 others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067525 | ||||||
| chr3:168067525
|
A | C | 30 | a0001c0001t0001g0194a0001c0001t0002g0027a0001c0001t0002g0034others(27): Show | 30 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.188-19160T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067525 | ||||||
| chr3:168067568
|
A | T | 1 | a0004c0004t0002g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.188-19203T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067568 | ||||||
| chr3:168067580
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-19215C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067580 | ||||||
| chr3:168067600
|
TTTTG | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-19239_188-1923 others(8): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067600 | ||||||
| chr3:168067660
|
T | C | 1 | a0001c0001t0003g0165 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.188-19295A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067660 | ||||||
| chr3:168067697
|
AAATGAAT others(5): Show |
A | 3 | a0002c0002t0020g0216a0002c0002t0026g0110a0004c0004t0020g0217 | 3 | HG03041.hp1 HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.188-19344_188-1933 others(16): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067697 | ||||||
| chr3:168067863
|
C | T | 7 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-19498G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168067863 | ||||||
| chr3:168068034
|
T | A | 1 | a0001c0001t0001g0181 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.188-19669A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068034 | ||||||
| chr3:168068377
|
A | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.188-20012T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068377 | ||||||
| chr3:168068396
|
A | G | 8 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0084others(5): Show | 8 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-20031T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068396 | ||||||
| chr3:168068474
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-20109T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068474 | ||||||
| chr3:168068550
|
C | T | 1 | a0001c0001t0012g0005 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.188-20185G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068550 | ||||||
| chr3:168068571
|
G | GT | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-20207dupA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068571 | ||||||
| chr3:168068770
|
T | C | 1 | a0001c0001t0027g0118 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.188-20405A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068770 | ||||||
| chr3:168068813
|
CTTTAA | C | 15 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-20453_188-2044 others(9): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068813 | ||||||
| chr3:168068829
|
T | C | 3 | a0001c0001t0012g0005a0001c0001t0012g0006a0001c0001t0012g0007 | 3 | HG02258.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.188-20464A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068829 | ||||||
| chr3:168068837
|
AT | A | 9 | a0001c0001t0001g0182a0001c0001t0002g0034a0001c0001t0002g0120others(6): Show | 9 | HG00323.hp1 HG01243.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-20473delA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068837 | ||||||
| chr3:168068841
|
T | A | 15 | a0001c0001t0002g0159a0001c0001t0005g0137a0001c0001t0007g0160others(12): Show | 15 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-20476A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068841 | ||||||
| chr3:168068842
|
T | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(92): Show | 97 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.188-20477A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068842 | ||||||
| chr3:168068843
|
T | A | 6 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(3): Show | 6 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-20478A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068843 | ||||||
| chr3:168068847
|
T | A | 20 | a0001c0001t0001g0194a0001c0001t0002g0027a0001c0001t0002g0116others(17): Show | 20 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.188-20482A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068847 | ||||||
| chr3:168068855
|
A | G | 44 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(41): Show | 45 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.188-20490T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068855 | ||||||
| chr3:168068874
|
T | C | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-20509A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068874 | ||||||
| chr3:168068998
|
G | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-20633C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168068998 | ||||||
| chr3:168069108
|
C | A | 4 | a0001c0001t0004g0090a0001c0001t0004g0092a0001c0001t0015g0089others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-20743G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168069108 | ||||||
| chr3:168069154
|
C | T | 1 | a0001c0001t0014g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.188-20789G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168069154 | ||||||
| chr3:168069271
|
G | A | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.188-20906C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168069271 | ||||||
| chr3:168069457
|
A | G | 1 | a0001c0005t0001g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.188-21092T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168069457 | ||||||
| chr3:168069777
|
T | TA | 123 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.188-21413dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168069777 | ||||||
| chr3:168069926
|
T | TAGAAAGA others(338): Show |
1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.188-21562_188-2156 others(349): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168069926 | ||||||
| chr3:168070030
|
C | T | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.188-21665G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168070030 | ||||||
| chr3:168070129
|
C | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-21764G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168070129 | ||||||
| chr3:168070253
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.188-21888G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168070253 | ||||||
| chr3:168070649
|
T | C | 1 | a0001c0010t0002g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-22284A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168070649 | ||||||
| chr3:168070767
|
T | C | 22 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(19): Show | 22 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.188-22402A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168070767 | ||||||
| chr3:168070789
|
T | G | 5 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-22424A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168070789 | ||||||
| chr3:168071180
|
G | T | 1 | a0004c0004t0038g0214 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188-22815C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071180 | ||||||
| chr3:168071263
|
C | G | 7 | a0001c0001t0001g0047a0001c0001t0003g0154a0001c0001t0006g0048others(4): Show | 7 | HG01257.hp2 HG01346.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-22898G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071263 | ||||||
| chr3:168071368
|
T | C | 49 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(46): Show | 49 | HG00140.hp1 HG00738.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.188-23003A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071368 | ||||||
| chr3:168071377
|
T | G | 1 | a0001c0001t0009g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.188-23012A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071377 | ||||||
| chr3:168071415
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.188-23050G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071415 | ||||||
| chr3:168071540
|
C | T | 5 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.188-23175G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071540 | ||||||
| chr3:168071717
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.188-23352C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071717 | ||||||
| chr3:168071756
|
T | C | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.187+23343A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071756 | ||||||
| chr3:168071899
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+23200G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071899 | ||||||
| chr3:168071939
|
G | T | 16 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(13): Show | 16 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.187+23160C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168071939 | ||||||
| chr3:168072017
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.187+23082A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072017 | ||||||
| chr3:168072034
|
C | T | 1 | a0004c0004t0007g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.187+23065G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072034 | ||||||
| chr3:168072105
|
T | C | 4 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+22994A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072105 | ||||||
| chr3:168072163
|
A | G | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.187+22936T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072163 | ||||||
| chr3:168072213
|
G | A | 1 | a0002c0002t0008g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.187+22886C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072213 | ||||||
| chr3:168072217
|
G | T | 1 | a0001c0001t0019g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.187+22882C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072217 | ||||||
| chr3:168072377
|
TA | T | 9 | a0001c0001t0001g0047a0001c0001t0001g0171a0001c0001t0004g0135others(6): Show | 9 | HG01069.hp2 HG01123.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.187+22721delT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072377 | ||||||
| chr3:168072584
|
A | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+22515T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072584 | ||||||
| chr3:168072800
|
T | C | 1 | a0003c0003t0005g0145 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.187+22299A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072800 | ||||||
| chr3:168072905
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(138): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.187+22194C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072905 | ||||||
| chr3:168072955
|
T | C | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+22144A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072955 | ||||||
| chr3:168072988
|
T | C | 25 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0002g0159others(22): Show | 25 | HG01167.hp1 HG01169.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.187+22111A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168072988 | ||||||
| chr3:168073205
|
T | C | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+21894A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073205 | ||||||
| chr3:168073210
|
C | T | 8 | a0001c0001t0002g0208a0001c0001t0005g0115a0001c0001t0012g0005others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+21889G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073210 | ||||||
| chr3:168073225
|
C | T | 1 | a0006c0007t0002g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.187+21874G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073225 | ||||||
| chr3:168073274
|
T | C | 1 | a0001c0001t0001g0149 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.187+21825A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073274 | ||||||
| chr3:168073460
|
C | G | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.187+21639G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073460 | ||||||
| chr3:168073570
|
C | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.187+21529G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073570 | ||||||
| chr3:168073616
|
G | T | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.187+21483C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073616 | ||||||
| chr3:168073813
|
C | T | 1 | a0001c0001t0003g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.187+21286G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073813 | ||||||
| chr3:168073814
|
A | G | 22 | a0001c0001t0001g0042a0001c0001t0001g0058a0001c0001t0003g0019others(19): Show | 22 | HG00735.hp1 HG00741.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.187+21285T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073814 | ||||||
| chr3:168073857
|
A | G | 8 | a0001c0001t0002g0208a0001c0001t0005g0115a0001c0001t0012g0005others(5): Show | 8 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+21242T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073857 | ||||||
| chr3:168073886
|
G | A | 7 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+21213C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073886 | ||||||
| chr3:168073947
|
A | G | 1 | a0004c0004t0002g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187+21152T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168073947 | ||||||
| chr3:168074048
|
A | C | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+21051T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168074048 | ||||||
| chr3:168074084
|
T | C | 4 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+21015A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168074084 | ||||||
| chr3:168074095
|
C | T | 1 | a0001c0001t0019g0119 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.187+21004G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168074095 | ||||||
| chr3:168074218
|
T | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+20881A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168074218 | ||||||
| chr3:168074374
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(56): Show | 60 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.187+20725A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168074374 | ||||||
| chr3:168074493
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.187+20606C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168074493 | ||||||
| chr3:168074616
|
A | G | 2 | a0001c0001t0002g0027a0001c0001t0002g0116 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.187+20483T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168074616 | ||||||
| chr3:168074883
|
G | C | 7 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+20216C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168074883 | ||||||
| chr3:168074964
|
G | C | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.187+20135C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168074964 | ||||||
| chr3:168075286
|
G | GT | 49 | a0001c0001t0001g0035a0001c0001t0001g0045a0001c0001t0001g0153others(46): Show | 49 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.187+19812dupA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075286 | ||||||
| chr3:168075286
|
G | GTT | 23 | a0001c0001t0002g0034a0001c0001t0002g0159a0001c0001t0004g0030others(20): Show | 23 | HG00140.hp1 HG01123.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.187+19811_187+1981 others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075286 | ||||||
| chr3:168075286
|
G | GTTT | 6 | a0001c0001t0014g0096a0002c0002t0005g0103a0002c0002t0005g0104others(3): Show | 6 | HG02055.hp1 HG02257.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+19810_187+1981 others(7): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075286 | ||||||
| chr3:168075286
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0004g0206 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.187+19803_187+1981 others(14): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075286 | ||||||
| chr3:168075286
|
GTTTTTTT others(4): Show |
G | 55 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(52): Show | 56 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.187+19802_187+1981 others(15): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075286 | ||||||
| chr3:168075389
|
C | T | 1 | a0001c0001t0004g0155 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.187+19710G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075389 | ||||||
| chr3:168075390
|
G | A | 5 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(2): Show | 5 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+19709C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075390 | ||||||
| chr3:168075441
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0011g0024 | 2 | HG00642.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.187+19658G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075441 | ||||||
| chr3:168075442
|
A | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+19657T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075442 | ||||||
| chr3:168075457
|
C | T | 9 | a0001c0001t0004g0062a0001c0001t0004g0063a0001c0001t0004g0090others(6): Show | 9 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.187+19642G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075457 | ||||||
| chr3:168075462
|
A | G | 1 | a0004c0004t0002g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187+19637T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075462 | ||||||
| chr3:168075500
|
G | A | 1 | a0004c0004t0038g0214 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.187+19599C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075500 | ||||||
| chr3:168075509
|
G | A | 2 | a0003c0003t0005g0145a0003c0003t0013g0144 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.187+19590C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075509 | ||||||
| chr3:168075544
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.187+19555A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075544 | ||||||
| chr3:168075557
|
C | T | 1 | a0001c0001t0032g0207 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.187+19542G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075557 | ||||||
| chr3:168075558
|
A | G | 15 | a0001c0001t0016g0003a0002c0002t0002g0109a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.187+19541T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075558 | ||||||
| chr3:168075623
|
A | T | 3 | a0005c0006t0008g0038a0005c0006t0008g0039a0005c0006t0008g0133 | 3 | HG01123.hp2 NA18956.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.187+19476T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075623 | ||||||
| chr3:168075655
|
A | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(68): Show | 72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.187+19444T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075655 | ||||||
| chr3:168075710
|
C | T | 123 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+19389G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168075710 | ||||||
| chr3:168076416
|
G | T | 1 | a0001c0001t0007g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.187+18683C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168076416 | ||||||
| chr3:168076583
|
C | T | 4 | a0001c0001t0001g0166a0001c0001t0006g0017a0001c0001t0006g0112others(1): Show | 4 | HG01175.hp1 HG01978.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+18516G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168076583 | ||||||
| chr3:168076682
|
C | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.187+18417G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168076682 | ||||||
| chr3:168076688
|
CTCAATCA others(1): Show |
C | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.187+18403_187+1841 others(12): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168076688 | ||||||
| chr3:168076717
|
T | C | 16 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(13): Show | 16 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.187+18382A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168076717 | ||||||
| chr3:168077214
|
T | C | 1 | a0001c0001t0004g0192 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.187+17885A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077214 | ||||||
| chr3:168077262
|
G | A | 3 | a0001c0001t0016g0004a0001c0001t0019g0119a0002c0002t0005g0124 | 3 | HG02622.hp2 HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.187+17837C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077262 | ||||||
| chr3:168077355
|
T | C | 3 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0019g0079 | 3 | HG01243.hp2 HG02145.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.187+17744A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077355 | ||||||
| chr3:168077398
|
C | G | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+17701G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077398 | ||||||
| chr3:168077708
|
C | G | 9 | a0001c0001t0007g0036a0001c0001t0007g0037a0001c0001t0007g0084others(6): Show | 9 | HG01255.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+17391G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077708 | ||||||
| chr3:168077721
|
T | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.187+17378A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077721 | ||||||
| chr3:168077740
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.187+17359A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077740 | ||||||
| chr3:168077811
|
T | C | 4 | a0002c0002t0001g0211a0002c0002t0002g0209a0002c0002t0002g0210others(1): Show | 4 | HG02055.hp2 HG02615.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+17288A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077811 | ||||||
| chr3:168077921
|
A | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(67): Show | 71 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.187+17178T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077921 | ||||||
| chr3:168077971
|
A | ATATT | 2 | a0001c0001t0001g0061a0001c0001t0011g0126 | 2 | HG00099.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.187+17124_187+1712 others(8): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168077971 | ||||||
| chr3:168078246
|
T | C | 7 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(4): Show | 7 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+16853A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078246 | ||||||
| chr3:168078299
|
T | C | 7 | a0001c0001t0002g0034a0001c0001t0002g0120a0001c0001t0011g0126others(4): Show | 7 | HG01243.hp2 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+16800A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078299 | ||||||
| chr3:168078321
|
A | G | 1 | a0001c0001t0021g0220 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.187+16778T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078321 | ||||||
| chr3:168078369
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(160): Show | 165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.187+16730G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078369 | ||||||
| chr3:168078497
|
A | G | 16 | a0001c0001t0004g0028a0001c0001t0004g0030a0001c0001t0004g0031others(13): Show | 16 | HG00140.hp1 HG00738.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.187+16602T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078497 | ||||||
| chr3:168078525
|
T | C | 8 | a0001c0001t0001g0058a0001c0001t0003g0022a0001c0001t0003g0054others(5): Show | 8 | HG01106.hp2 HG02602.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+16574A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078525 | ||||||
| chr3:168078593
|
A | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0161a0001c0001t0001g0162others(2): Show | 5 | HG00099.hp2 HG00323.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+16506T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078593 | ||||||
| chr3:168078602
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.187+16497C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078602 | ||||||
| chr3:168078793
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.187+16306C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078793 | ||||||
| chr3:168078812
|
G | C | 2 | a0002c0002t0008g0121a0002c0002t0022g0221 | 2 | HG01884.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.187+16287C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078812 | ||||||
| chr3:168078858
|
C | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.187+16241G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078858 | ||||||
| chr3:168078898
|
C | T | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.187+16201G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078898 | ||||||
| chr3:168078951
|
TTG | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.187+16146_187+1614 others(6): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078951 | ||||||
| chr3:168078963
|
T | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.187+16136A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078963 | ||||||
| chr3:168078988
|
A | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.187+16111T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168078988 | ||||||
| chr3:168079101
|
A | G | 7 | a0001c0001t0002g0208a0001c0001t0012g0005a0001c0001t0012g0006others(4): Show | 7 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.187+15998T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079101 | ||||||
| chr3:168079254
|
A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.187+15845T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079254 | ||||||
| chr3:168079258
|
A | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(102): Show | 106 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.187+15841T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079258 | ||||||
| chr3:168079357
|
A | G | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+15742T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079357 | ||||||
| chr3:168079386
|
C | T | 8 | a0003c0003t0005g0145a0003c0003t0005g0197a0003c0003t0005g0198others(5): Show | 8 | HG02071.hp1 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+15713G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079386 | ||||||
| chr3:168079521
|
G | A | 2 | a0004c0004t0011g0193a0004c0004t0043g0225 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.187+15578C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079521 | ||||||
| chr3:168079554
|
T | C | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+15545A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079554 | ||||||
| chr3:168079650
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0025others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.187+15449A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079650 | ||||||
| chr3:168079761
|
T | C | 2 | a0001c0001t0001g0194a0001c0001t0004g0071 | 2 | NA18963.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.187+15338A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079761 | ||||||
| chr3:168079828
|
T | A | 9 | a0001c0001t0002g0136a0001c0001t0002g0196a0001c0001t0008g0101others(6): Show | 10 | HG02451.hp1 HG02622.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.187+15271A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079828 | ||||||
| chr3:168079891
|
G | A | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.187+15208C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079891 | ||||||
| chr3:168079899
|
A | G | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0004c0004t0002g0139 | 3 | HG02723.hp2 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.187+15200T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168079899 | ||||||
| chr3:168080033
|
T | G | 25 | a0001c0001t0001g0073a0001c0001t0008g0125a0001c0001t0016g0003others(22): Show | 26 | HG01243.hp1 HG02040.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.187+15066A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080033 | ||||||
| chr3:168080035
|
T | C | 1 | a0004c0004t0002g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187+15064A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080035 | ||||||
| chr3:168080100
|
G | T | 3 | a0001c0001t0002g0027a0001c0001t0002g0116a0001c0001t0004g0028 | 3 | HG02723.hp2 HG03017.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.187+14999C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080100 | ||||||
| chr3:168080161
|
A | G | 1 | a0001c0001t0015g0089 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.187+14938T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080161 | ||||||
| chr3:168080191
|
G | C | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.187+14908C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080191 | ||||||
| chr3:168080250
|
A | T | 1 | a0001c0001t0030g0127 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.187+14849T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080250 | ||||||
| chr3:168080413
|
T | C | 1 | a0001c0010t0002g0083 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.187+14686A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080413 | ||||||
| chr3:168080440
|
T | C | 1 | a0001c0001t0003g0200 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.187+14659A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080440 | ||||||
| chr3:168080614
|
C | CA | 15 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0005g0137others(12): Show | 15 | HG01433.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.187+14484_187+1448 others(5): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080614 | ||||||
| chr3:168080769
|
C | T | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.187+14330G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080769 | ||||||
| chr3:168080810
|
CCATA | C | 19 | a0001c0001t0005g0115a0001c0001t0008g0125a0001c0001t0012g0005others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.187+14285_187+1428 others(8): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080810 | ||||||
| chr3:168080826
|
G | A | 12 | a0001c0001t0012g0005a0001c0001t0012g0006a0001c0001t0012g0007others(9): Show | 12 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+14273C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168080826 | ||||||
| chr3:168081328
|
G | A | 2 | a0002c0002t0005g0124a0004c0004t0002g0139 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.187+13771C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081328 | ||||||
| chr3:168081386
|
T | A | 1 | a0001c0005t0001g0074 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.187+13713A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081386 | ||||||
| chr3:168081395
|
T | C | 15 | a0001c0001t0002g0208a0001c0001t0018g0001a0001c0001t0022g0223others(12): Show | 16 | HG00558.hp2 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.187+13704A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081395 | ||||||
| chr3:168081412
|
G | C | 2 | a0001c0001t0022g0223a0001c0001t0042g0222 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.187+13687C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081412 | ||||||
| chr3:168081498
|
A | G | 1 | a0001c0001t0006g0075 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.187+13601T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081498 | ||||||
| chr3:168081516
|
G | T | 1 | a0002c0002t0005g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.187+13583C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081516 | ||||||
| chr3:168081535
|
T | C | 2 | a0001c0001t0003g0076a0001c0001t0009g0077 | 2 | NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.187+13564A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081535 | ||||||
| chr3:168081635
|
C | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.187+13464G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081635 | ||||||
| chr3:168081742
|
T | A | 3 | a0001c0001t0008g0125a0001c0001t0018g0001a0002c0002t0024g0012 | 4 | HG02896.hp2 HG02897.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+13357A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081742 | ||||||
| chr3:168081760
|
A | C | 1 | a0001c0001t0016g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.187+13339T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081760 | ||||||
| chr3:168081770
|
T | C | 1 | a0001c0001t0006g0075 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.187+13329A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168081770 | ||||||
| chr3:168082114
|
T | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(117): Show | 121 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.187+12985A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082114 | ||||||
| chr3:168082285
|
C | T | 1 | a0001c0001t0044g0226 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.187+12814G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082285 | ||||||
| chr3:168082321
|
A | G | 2 | a0002c0002t0005g0124a0004c0004t0002g0139 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.187+12778T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082321 | ||||||
| chr3:168082336
|
C | G | 1 | a0001c0001t0011g0024 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.187+12763G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082336 | ||||||
| chr3:168082372
|
C | T | 4 | a0001c0001t0004g0090a0001c0001t0004g0092a0001c0001t0015g0089others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+12727G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082372 | ||||||
| chr3:168082393
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0010g0023 | 2 | HG01169.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.187+12706A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082393 | ||||||
| chr3:168082502
|
T | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.187+12597A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082502 | ||||||
| chr3:168082510
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.187+12589A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082510 | ||||||
| chr3:168082748
|
C | T | 3 | a0001c0001t0005g0115a0002c0002t0005g0124a0004c0004t0002g0139 | 3 | HG02486.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.187+12351G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082748 | ||||||
| chr3:168082749
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(117): Show | 121 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.187+12350T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168082749 | ||||||
| chr3:168083282
|
C | CA | 8 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0014g0117others(5): Show | 8 | HG01884.hp2 HG03195.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+11816dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168083282 | ||||||
| chr3:168083322
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.187+11777G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168083322 | ||||||
| chr3:168083367
|
C | T | 6 | a0001c0001t0012g0005a0001c0001t0012g0006a0001c0001t0012g0007others(3): Show | 6 | HG02109.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+11732G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168083367 | ||||||
| chr3:168083650
|
G | C | 47 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(44): Show | 48 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(45): Show |
intron_variant | MODIFIER | c.187+11449C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168083650 | ||||||
| chr3:168083676
|
T | C | 2 | a0001c0001t0018g0001a0002c0002t0024g0012 | 3 | HG02896.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.187+11423A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168083676 | ||||||
| chr3:168083873
|
G | C | 5 | a0001c0001t0002g0208a0002c0002t0001g0211a0002c0002t0002g0209others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+11226C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168083873 | ||||||
| chr3:168083995
|
A | G | 2 | a0001c0001t0022g0223a0001c0001t0042g0222 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.187+11104T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168083995 | ||||||
| chr3:168084039
|
T | C | 45 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(42): Show | 46 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(43): Show |
intron_variant | MODIFIER | c.187+11060A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084039 | ||||||
| chr3:168084076
|
T | C | 1 | a0001c0001t0044g0226 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.187+11023A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084076 | ||||||
| chr3:168084084
|
C | T | 18 | a0001c0001t0002g0100a0001c0001t0007g0111a0001c0001t0008g0098others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.187+11015G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084084 | ||||||
| chr3:168084207
|
T | C | 1 | a0001c0001t0009g0202 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.187+10892A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084207 | ||||||
| chr3:168084229
|
T | C | 47 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(44): Show | 48 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(45): Show |
intron_variant | MODIFIER | c.187+10870A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084229 | ||||||
| chr3:168084426
|
C | T | 45 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(42): Show | 46 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(43): Show |
intron_variant | MODIFIER | c.187+10673G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084426 | ||||||
| chr3:168084529
|
A | G | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+10570T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084529 | ||||||
| chr3:168084601
|
T | C | 1 | a0001c0001t0006g0151 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.187+10498A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084601 | ||||||
| chr3:168084698
|
A | G | 55 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(52): Show | 56 | HG00558.hp2 HG01123.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.187+10401T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084698 | ||||||
| chr3:168084958
|
A | T | 1 | a0001c0001t0011g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.187+10141T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084958 | ||||||
| chr3:168084988
|
C | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(119): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+10111G>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168084988 | ||||||
| chr3:168085293
|
T | C | 2 | a0001c0001t0014g0143a0001c0001t0017g0142 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.187+9806A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168085293 | ||||||
| chr3:168085327
|
A | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(119): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+9772T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168085327 | ||||||
| chr3:168085342
|
C | A | 2 | a0001c0001t0003g0076a0001c0001t0009g0077 | 2 | NA19012.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.187+9757G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168085342 | ||||||
| chr3:168085422
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.187+9677C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168085422 | ||||||
| chr3:168085540
|
C | A | 2 | a0001c0001t0018g0001a0002c0002t0024g0012 | 3 | HG02896.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.187+9559G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168085540 | ||||||
| chr3:168085589
|
C | T | 1 | a0001c0001t0003g0154 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.187+9510G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168085589 | ||||||
| chr3:168085882
|
G | A | 2 | a0001c0001t0039g0215a0004c0004t0038g0214 | 2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.187+9217C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168085882 | ||||||
| chr3:168085883
|
C | T | 5 | a0001c0001t0022g0223a0001c0001t0042g0222a0002c0002t0022g0221others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+9216G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168085883 | ||||||
| chr3:168085931
|
A | G | 13 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0003g0128others(10): Show | 13 | HG01123.hp2 HG01516.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.187+9168T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168085931 | ||||||
| chr3:168086153
|
A | C | 47 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(44): Show | 48 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(45): Show |
intron_variant | MODIFIER | c.187+8946T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168086153 | ||||||
| chr3:168086366
|
C | T | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+8733G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168086366 | ||||||
| chr3:168086478
|
T | C | 11 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0005g0115others(8): Show | 11 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.187+8621A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168086478 | ||||||
| chr3:168086486
|
C | T | 45 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(42): Show | 46 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(43): Show |
intron_variant | MODIFIER | c.187+8613G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168086486 | ||||||
| chr3:168086895
|
A | T | 3 | a0001c0001t0037g0213a0002c0002t0005g0140a0004c0004t0007g0141 | 3 | HG01433.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.187+8204T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168086895 | ||||||
| chr3:168086937
|
G | A | 3 | a0001c0001t0021g0218a0001c0001t0021g0220a0001c0001t0040g0219 | 3 | HG02258.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+8162C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168086937 | ||||||
| chr3:168087160
|
A | G | 1 | a0001c0001t0010g0023 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.187+7939T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087160 | ||||||
| chr3:168087210
|
T | C | 1 | a0001c0001t0019g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.187+7889A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087210 | ||||||
| chr3:168087236
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.187+7863T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087236 | ||||||
| chr3:168087240
|
A | G | 1 | a0001c0001t0008g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.187+7859T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087240 | ||||||
| chr3:168087339
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.187+7760C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087339 | ||||||
| chr3:168087351
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.187+7748A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087351 | ||||||
| chr3:168087392
|
C | T | 2 | a0001c0001t0011g0021a0001c0001t0015g0020 | 2 | HG02683.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.187+7707G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087392 | ||||||
| chr3:168087509
|
T | C | 1 | a0001c0001t0003g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.187+7590A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087509 | ||||||
| chr3:168087628
|
C | T | 1 | a0002c0002t0022g0221 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.187+7471G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087628 | ||||||
| chr3:168087868
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.187+7231G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168087868 | ||||||
| chr3:168088042
|
T | C | 55 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(52): Show | 56 | HG00558.hp2 HG01123.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.187+7057A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088042 | ||||||
| chr3:168088103
|
T | C | 45 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(42): Show | 46 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(43): Show |
intron_variant | MODIFIER | c.187+6996A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088103 | ||||||
| chr3:168088156
|
C | T | 1 | a0001c0001t0016g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+6943G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088156 | ||||||
| chr3:168088188
|
C | T | 22 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0003g0128others(19): Show | 22 | HG01123.hp2 HG01516.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.187+6911G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088188 | ||||||
| chr3:168088321
|
T | C | 1 | a0001c0001t0002g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.187+6778A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088321 | ||||||
| chr3:168088433
|
C | T | 225 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.187+6666G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088433 | ||||||
| chr3:168088614
|
C | A | 2 | a0001c0001t0007g0084a0001c0010t0002g0083 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.187+6485G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088614 | ||||||
| chr3:168088809
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.187+6290G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088809 | ||||||
| chr3:168088825
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.187+6274A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088825 | ||||||
| chr3:168088942
|
C | A | 8 | a0001c0001t0002g0208a0001c0001t0021g0218a0001c0001t0021g0220others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+6157G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168088942 | ||||||
| chr3:168089060
|
T | C | 55 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(52): Show | 56 | HG00558.hp2 HG01123.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.187+6039A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089060 | ||||||
| chr3:168089110
|
A | C | 1 | a0001c0001t0003g0019 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.187+5989T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089110 | ||||||
| chr3:168089168
|
T | C | 5 | a0001c0001t0001g0087a0001c0001t0006g0086a0001c0001t0006g0112others(2): Show | 5 | HG01175.hp1 HG01261.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+5931A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089168 | ||||||
| chr3:168089229
|
T | C | 1 | a0001c0001t0044g0226 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.187+5870A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089229 | ||||||
| chr3:168089387
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.187+5712G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089387 | ||||||
| chr3:168089528
|
G | C | 4 | a0001c0001t0004g0090a0001c0001t0004g0092a0001c0001t0015g0089others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+5571C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089528 | ||||||
| chr3:168089583
|
G | A | 1 | a0001c0001t0033g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.187+5516C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089583 | ||||||
| chr3:168089601
|
G | A | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+5498C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089601 | ||||||
| chr3:168089642
|
G | A | 1 | a0001c0001t0002g0138 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.187+5457C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089642 | ||||||
| chr3:168089766
|
T | C | 1 | a0001c0001t0008g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187+5333A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089766 | ||||||
| chr3:168089769
|
C | CT | 36 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0208others(33): Show | 36 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(33): Show |
intron_variant | MODIFIER | c.187+5329dupA | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089769 | ||||||
| chr3:168089769
|
C | CTT | 10 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0014g0117others(7): Show | 10 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.187+5328_187+5329d others(4): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089769 | ||||||
| chr3:168089787
|
G | C | 2 | a0001c0001t0039g0215a0004c0004t0038g0214 | 2 | HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.187+5312C>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089787 | ||||||
| chr3:168089800
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.187+5299C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168089800 | ||||||
| chr3:168090245
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.187+4854G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168090245 | ||||||
| chr3:168090304
|
T | A | 3 | a0001c0001t0004g0204a0001c0001t0004g0206a0001c0001t0034g0205 | 3 | HG00140.hp1 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.187+4795A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168090304 | ||||||
| chr3:168090330
|
G | GA | 45 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(42): Show | 46 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(43): Show |
intron_variant | MODIFIER | c.187+4768dupT | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168090330 | ||||||
| chr3:168090589
|
A | G | 2 | a0001c0001t0021g0218a0001c0001t0040g0219 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.187+4510T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168090589 | ||||||
| chr3:168090657
|
T | TC | 32 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0002g0208others(29): Show | 32 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.187+4441dupG | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168090657 | ||||||
| chr3:168090675
|
A | T | 1 | a0001c0001t0014g0096 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.187+4424T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168090675 | ||||||
| chr3:168090784
|
A | G | 9 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0006g0146others(6): Show | 9 | HG01257.hp2 HG01346.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.187+4315T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168090784 | ||||||
| chr3:168090809
|
A | G | 1 | a0003c0003t0013g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.187+4290T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168090809 | ||||||
| chr3:168090838
|
G | A | 24 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0003g0128others(21): Show | 24 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.187+4261C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168090838 | ||||||
| chr3:168091026
|
A | AG | 39 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(36): Show | 40 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(37): Show |
intron_variant | MODIFIER | c.187+4072dupC | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091026 | ||||||
| chr3:168091028
|
G | GA | 8 | a0001c0001t0002g0208a0001c0001t0021g0218a0001c0001t0021g0220others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+4070_187+4071i others(3): Show |
GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091028 | ||||||
| chr3:168091116
|
T | C | 5 | a0001c0001t0002g0208a0002c0002t0001g0211a0002c0002t0002g0209others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+3983A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091116 | ||||||
| chr3:168091132
|
A | G | 55 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(52): Show | 56 | HG00558.hp2 HG01123.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.187+3967T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091132 | ||||||
| chr3:168091197
|
T | C | 1 | a0001c0001t0044g0226 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.187+3902A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091197 | ||||||
| chr3:168091757
|
T | C | 22 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0003g0128others(19): Show | 22 | HG01123.hp2 HG01516.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.187+3342A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091757 | ||||||
| chr3:168091789
|
C | T | 55 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(52): Show | 56 | HG00558.hp2 HG01123.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.187+3310G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091789 | ||||||
| chr3:168091807
|
C | T | 1 | a0001c0001t0010g0016 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.187+3292G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091807 | ||||||
| chr3:168091841
|
A | C | 24 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0003g0128others(21): Show | 24 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(21): Show |
intron_variant | MODIFIER | c.187+3258T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091841 | ||||||
| chr3:168091986
|
G | T | 1 | a0001c0001t0005g0115 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.187+3113C>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168091986 | ||||||
| chr3:168092024
|
T | C | 1 | a0001c0001t0002g0095 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.187+3075A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168092024 | ||||||
| chr3:168092064
|
T | C | 1 | a0004c0004t0002g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187+3035A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168092064 | ||||||
| chr3:168092092
|
T | C | 13 | a0001c0001t0002g0136a0001c0001t0002g0138a0001c0001t0003g0128others(10): Show | 13 | HG01123.hp2 HG01516.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.187+3007A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168092092 | ||||||
| chr3:168092324
|
T | C | 18 | a0001c0001t0002g0100a0001c0001t0007g0111a0001c0001t0008g0098others(15): Show | 18 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.187+2775A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168092324 | ||||||
| chr3:168092533
|
A | G | 45 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(42): Show | 46 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(43): Show |
intron_variant | MODIFIER | c.187+2566T>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168092533 | ||||||
| chr3:168092778
|
A | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(119): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+2321T>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168092778 | ||||||
| chr3:168092833
|
TG | T | 11 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0005g0115others(8): Show | 11 | HG01884.hp2 HG02486.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.187+2265delC | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168092833 | ||||||
| chr3:168092869
|
T | G | 1 | a0004c0004t0002g0139 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.187+2230A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168092869 | ||||||
| chr3:168093135
|
T | A | 1 | a0001c0001t0032g0207 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.187+1964A>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168093135 | ||||||
| chr3:168093136
|
C | A | 1 | a0001c0001t0006g0112 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.187+1963G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168093136 | ||||||
| chr3:168093248
|
T | G | 8 | a0001c0001t0002g0208a0001c0001t0021g0218a0001c0001t0021g0220others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+1851A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168093248 | ||||||
| chr3:168093406
|
G | A | 2 | a0001c0001t0003g0113a0001c0001t0003g0114 | 2 | HG01167.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.187+1693C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168093406 | ||||||
| chr3:168093442
|
C | T | 2 | a0001c0001t0018g0001a0002c0002t0024g0012 | 3 | HG02896.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.187+1657G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168093442 | ||||||
| chr3:168093540
|
T | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.187+1559A>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168093540 | ||||||
| chr3:168093611
|
C | A | 8 | a0001c0001t0002g0208a0001c0001t0021g0218a0001c0001t0021g0220others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+1488G>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168093611 | ||||||
| chr3:168093779
|
G | A | 2 | a0001c0001t0018g0001a0002c0002t0024g0012 | 3 | HG02896.hp2 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.187+1320C>T | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168093779 | ||||||
| chr3:168093979
|
C | T | 2 | a0001c0001t0001g0014a0001c0008t0001g0015 | 2 | HG02040.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.187+1120G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168093979 | ||||||
| chr3:168094771
|
C | T | 40 | a0001c0001t0002g0116a0001c0001t0002g0120a0001c0001t0002g0136others(37): Show | 41 | HG00558.hp2 HG01123.hp2 HG01516.hp1 others(38): Show |
intron_variant | MODIFIER | c.187+328G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168094771 | ||||||
| chr3:168094854
|
A | C | 3 | a0001c0001t0012g0005a0001c0001t0012g0006a0001c0001t0012g0007 | 3 | HG02258.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.187+245T>G | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168094854 | ||||||
| chr3:168094948
|
T | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(119): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+151A>C | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168094948 | ||||||
| chr3:168095022
|
C | T | 2 | a0001c0001t0016g0003a0001c0001t0016g0004 | 2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.187+77G>A | GOLIM4 | ENSG00000173905.9 | transcript | ENST00000470487.6 | protein_coding | 1/15 | chr3 | 168095022 |