| geneid | 3973 |
|---|---|
| ensemblid | ENSG00000138039.15 |
| hgncid | 6585 |
| symbol | LHCGR |
| name | luteinizing hormone/choriogonadotropin receptor |
| refseq_nuc | NM_000233.4 |
| refseq_prot | NP_000224.2 |
| ensembl_nuc | ENST00000294954.12 |
| ensembl_prot | ENSP00000294954.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 48686774 |
| end | 48755724 |
| strand | - |
| ver | v1.2 |
| region | chr2:48686774-48755724 |
| region5000 | chr2:48681774-48760724 |
| regionname0 | LHCGR_chr2_48686774_48755724 |
| regionname5000 | LHCGR_chr2_48681774_48760724 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 699 | 218 | 16 | 44 | 134 | 7 | 17 | 87 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002 | 1/1 | 699 | 115 | 58 | 17 | 16 | 3 | 19 | 13 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0003 | 0/0 | 701 | 18 | 9 | 6 | 0 | 2 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0004 | 0/0 | 701 | 15 | 3 | 7 | 0 | 0 | 5 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0005 | 0/0 | 701 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0006 | 0/0 | 699 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0007 | 0/0 | 699 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2100 | 213 | 16 | 43 | 132 | 7 | 15 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0002 | 1/1 | 2100 | 108 | 53 | 17 | 15 | 3 | 18 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0003 | 0/0 | 2106 | 17 | 8 | 6 | 0 | 2 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0004 | 0/0 | 2106 | 15 | 3 | 7 | 0 | 0 | 5 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0005 | 0/0 | 2100 | 4 | 2 | 0 | 1 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0006 | 0/0 | 2100 | 4 | 0 | 0 | 2 | 0 | 2 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0007 | 0/0 | 2100 | 3 | 1 | 2 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0008 | 0/0 | 2106 | 3 | 3 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0009 | 0/0 | 2100 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0010 | 0/0 | 2100 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0011 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0012 | 0/0 | 2100 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| c0013 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 977 | 269 | 45 | 53 | 131 | 10 | 29 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| t0002 | 0/1 | 977 | 52 | 2 | 18 | 16 | 2 | 13 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| t0003 | 0/0 | 977 | 23 | 20 | 3 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| t0004 | 0/0 | 977 | 19 | 18 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| t0005 | 0/0 | 977 | 5 | 5 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| t0006 | 0/0 | 976 | 3 | 0 | 0 | 3 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| t0007 | 0/0 | 977 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| t0008 | 0/0 | 977 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| t0009 | 0/0 | 977 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| 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 | 3 | 2 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0308 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2100 | 213 | 16 | 43 | 132 | 7 | 15 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0001c0006 | 0/0 | 2100 | 4 | 0 | 0 | 2 | 0 | 2 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0001c0012 | 0/0 | 2100 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0002 | 1/1 | 2100 | 108 | 53 | 17 | 15 | 3 | 18 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0005 | 0/0 | 2100 | 4 | 2 | 0 | 1 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0010 | 0/0 | 2100 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0011 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0003c0003 | 0/0 | 2106 | 17 | 8 | 6 | 0 | 2 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0003c0013 | 0/0 | 2106 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0004c0004 | 0/0 | 2106 | 15 | 3 | 7 | 0 | 0 | 5 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0005c0008 | 0/0 | 2106 | 3 | 3 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0006c0007 | 0/0 | 2100 | 3 | 1 | 2 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0007c0009 | 0/0 | 2100 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3076 | 208 | 15 | 42 | 129 | 7 | 15 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0001c0001t0006 | 0/0 | 3075 | 3 | 0 | 0 | 3 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0001c0001t0007 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0001c0001t0009 | 0/0 | 3076 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0001c0006t0001 | 0/0 | 3076 | 4 | 0 | 0 | 2 | 0 | 2 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0001c0012t0001 | 0/0 | 3076 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0002t0001 | 1/0 | 3076 | 32 | 22 | 3 | 0 | 1 | 5 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0002t0002 | 0/1 | 3076 | 46 | 2 | 13 | 15 | 2 | 13 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0002t0003 | 0/0 | 3076 | 13 | 12 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0002t0004 | 0/0 | 3076 | 11 | 11 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0002t0005 | 0/0 | 3076 | 5 | 5 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0002t0008 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0005t0001 | 0/0 | 3076 | 3 | 2 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0005t0002 | 0/0 | 3076 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0010t0001 | 0/0 | 3076 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0002c0011t0003 | 0/0 | 3076 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0003c0003t0001 | 0/0 | 3082 | 4 | 1 | 0 | 0 | 2 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0003c0003t0002 | 0/0 | 3082 | 5 | 0 | 5 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0003c0003t0003 | 0/0 | 3082 | 5 | 5 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0003c0003t0004 | 0/0 | 3082 | 3 | 2 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0003c0013t0003 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0004c0004t0001 | 0/0 | 3082 | 15 | 3 | 7 | 0 | 0 | 5 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0005c0008t0004 | 0/0 | 3082 | 3 | 3 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0006c0007t0003 | 0/0 | 3076 | 3 | 1 | 2 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| a0007c0009t0004 | 0/0 | 3076 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | copy fasta | chr2 | 48681774 | 48760724 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0001t0009g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0006t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0006t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0006t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0001c0012t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0308 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0002t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0005t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0005t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0010t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0010t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0002c0011t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0003t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0003c0013t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0004c0004t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0005c0008t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0005c0008t0004g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0006c0007t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0006c0007t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0006c0007t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0007c0009t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| a0007c0009t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0237 | EUR | GBR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | FIN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00639 | hp2 | a0004 | c0004 | t0001 | g0336 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0242 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00733 | hp1 | a0004 | c0004 | t0001 | g0345 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0268 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0322 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0137 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01069 | hp1 | a0003 | c0003 | t0002 | g0347 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01070 | hp2 | a0006 | c0007 | t0003 | g0316 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0346 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0310 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01106 | hp2 | a0002 | c0002 | t0002 | g0191 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0284 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0281 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01168 | hp2 | a0004 | c0004 | t0001 | g0332 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01169 | hp1 | a0004 | c0004 | t0001 | g0351 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01175 | hp2 | a0004 | c0004 | t0001 | g0339 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0112 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01243 | hp2 | a0003 | c0003 | t0004 | g0342 | AMR | PUR | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0167 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0354 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01257 | hp1 | a0003 | c0003 | t0002 | g0355 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01261 | hp1 | a0004 | c0004 | t0001 | g0335 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0150 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01496 | hp2 | a0004 | c0004 | t0001 | g0356 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0357 | EUR | IBS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0330 | EUR | IBS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0097 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0078 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0217 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01952 | hp2 | a0003 | c0003 | t0002 | g0340 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01975 | hp1 | a0001 | c0012 | t0001 | g0023 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0179 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0323 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02055 | hp2 | a0007 | c0009 | t0004 | g0099 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02145 | hp1 | a0002 | c0002 | t0005 | g0067 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CDX | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02258 | hp1 | a0002 | c0010 | t0001 | g0211 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0115 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0358 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0297 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0109 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0223 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02602 | hp2 | a0001 | c0006 | t0001 | g0225 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02615 | hp2 | a0003 | c0013 | t0003 | g0341 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02622 | hp1 | a0003 | c0003 | t0003 | g0331 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02622 | hp2 | a0002 | c0002 | t0004 | g0232 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02630 | hp1 | a0002 | c0002 | t0005 | g0250 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02647 | hp1 | a0002 | c0002 | t0004 | g0005 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02647 | hp2 | a0002 | c0002 | t0005 | g0081 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02683 | hp1 | a0004 | c0004 | t0001 | g0337 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0229 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0311 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02698 | hp2 | a0004 | c0004 | t0001 | g0359 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02723 | hp2 | a0002 | c0002 | t0003 | g0293 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02809 | hp1 | a0002 | c0002 | t0003 | g0065 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0064 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0204 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02895 | hp2 | a0004 | c0004 | t0001 | g0352 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0208 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02896 | hp2 | a0002 | c0002 | t0005 | g0326 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0128 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02922 | hp1 | a0003 | c0003 | t0003 | g0348 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02922 | hp2 | a0002 | c0002 | t0004 | g0068 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02965 | hp1 | a0003 | c0003 | t0004 | g0338 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02965 | hp2 | a0002 | c0002 | t0004 | g0074 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0210 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02976 | hp1 | a0002 | c0005 | t0001 | g0206 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02976 | hp2 | a0002 | c0002 | t0004 | g0080 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0200 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03017 | hp2 | a0004 | c0004 | t0001 | g0333 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0270 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03041 | hp2 | a0004 | c0004 | t0001 | g0328 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03098 | hp1 | a0002 | c0011 | t0003 | g0249 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03098 | hp2 | a0002 | c0005 | t0001 | g0066 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03130 | hp2 | a0004 | c0004 | t0001 | g0344 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03139 | hp1 | a0005 | c0008 | t0004 | g0012 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03139 | hp2 | a0002 | c0002 | t0008 | g0098 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0247 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03209 | hp1 | a0002 | c0002 | t0004 | g0294 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03225 | hp1 | a0005 | c0008 | t0004 | g0361 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03225 | hp2 | a0002 | c0002 | t0005 | g0213 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03453 | hp1 | a0003 | c0003 | t0003 | g0360 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0170 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03486 | hp2 | a0005 | c0008 | t0004 | g0012 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03516 | hp1 | a0002 | c0002 | t0004 | g0189 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0139 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03540 | hp2 | a0002 | c0010 | t0001 | g0212 | AFR | GWD | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0315 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0127 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03688 | hp1 | a0002 | c0005 | t0001 | g0148 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03704 | hp1 | a0004 | c0004 | t0001 | g0349 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0324 | SAS | PJL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03831 | hp2 | a0003 | c0003 | t0001 | g0353 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0084 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04115 | hp1 | a0001 | c0006 | t0001 | g0151 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0325 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04184 | hp1 | a0004 | c0004 | t0001 | g0350 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0276 | SAS | BEB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0149 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0161 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0307 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0145 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0009 | SAS | STU | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0343 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0283 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0171 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18940 | hp1 | a0001 | c0006 | t0001 | g0288 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18995 | hp1 | a0002 | c0005 | t0002 | g0144 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19011 | hp1 | a0001 | c0006 | t0001 | g0260 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19030 | hp1 | a0003 | c0003 | t0003 | g0329 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19030 | hp2 | a0007 | c0009 | t0004 | g0069 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0224 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19086 | hp1 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19086 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0295 | AFR | ASW | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ASW | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0302 | EUR | TSI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0313 | EUR | TSI | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | GIH | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | GIH | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01123 | hp1 | a0006 | c0007 | t0003 | g0047 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0245 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0317 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0261 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG02559 | hp2 | a0003 | c0003 | t0004 | g0334 | AFR | ACB | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03471 | hp1 | a0002 | c0002 | t0004 | g0076 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0110 | AFR | MSL | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG06807 | hp1 | a0002 | c0002 | t0004 | g0005 | AFR | USA | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| HG06807 | hp2 | a0002 | c0002 | t0003 | g0262 | AFR | USA | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0070 | AFR | USA | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0014 | AFR | USA | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA21309 | hp1 | a0006 | c0007 | t0003 | g0296 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0308 | REF | REF | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0243 | REF | REF | LHCGR_chr2_48681774_48760724 | LHCGR | chr2 | 48681774 | 48760724 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48694236
|
T | C | 2 | a0001a0004 | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
missense_variant | MODERATE | c.935A>G | p.Asn312Ser | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/11 | 988/3076 | 935/2100 | 312/699 | chr2 | 48694236 | ||
| chr2:48694299
|
T | C | 1 | a0006 | 3 | HG01070.hp2 HG01123.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.872A>G | p.Asn291Ser | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/11 | 925/3076 | 872/2100 | 291/699 | chr2 | 48694299 | ||
| chr2:48709006
|
C | T | 2 | a0005a0007 | 5 | HG02055.hp2 HG03139.hp1 HG03225.hp1 others(2): Show |
missense_variant | MODERATE | c.622G>A | p.Val208Ile | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/11 | 675/3076 | 622/2100 | 208/699 | chr2 | 48709006 | ||
| chr2:48755616
|
G | GGCTGCA | 3 | a0003a0004a0005 | 36 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(33): Show |
conservative_inframe_insertion | MODERATE | c.50_55dupTGCAGC | p.Leu17_Gln18dup | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/11 | 108/3076 | 55/2100 | 19/699 | chr2 | 48755616 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48687928
|
A | G | 1 | a0002c0011 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1869T>C | p.Tyr623Tyr | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 1922/3076 | 1869/2100 | 623/699 | chr2 | 48687928 | ||
| chr2:48688684
|
A | G | 1 | a0002c0010 | 2 | HG02258.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.1113T>C | p.Ile371Ile | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 1166/3076 | 1113/2100 | 371/699 | chr2 | 48688684 | ||
| chr2:48688732
|
A | G | 4 | a0001c0001a0001c0012a0002c0005others(1): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
synonymous_variant | LOW | c.1065T>C | p.Asp355Asp | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 1118/3076 | 1065/2100 | 355/699 | chr2 | 48688732 | ||
| chr2:48698710
|
T | C | 1 | a0001c0012 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.771A>G | p.Lys257Lys | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/11 | 824/3076 | 771/2100 | 257/699 | chr2 | 48698710 | ||
| chr2:48723654
|
C | T | 1 | a0003c0013 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.426G>A | p.Thr142Thr | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 5/11 | 479/3076 | 426/2100 | 142/699 | chr2 | 48723654 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48687013
|
T | A | 1 | a0001c0001t0009 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*684A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 684 | chr2 | 48687013 | |||||
| chr2:48687169
|
A | G | 5 | a0002c0002t0004a0002c0002t0008a0003c0003t0004others(2): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*528T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 528 | chr2 | 48687169 | |||||
| chr2:48687207
|
T | G | 1 | a0002c0002t0008 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*490A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 490 | chr2 | 48687207 | |||||
| chr2:48687337
|
C | T | 5 | a0002c0002t0004a0002c0002t0008a0003c0003t0004others(2): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*360G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 360 | chr2 | 48687337 | |||||
| chr2:48687415
|
GT | G | 1 | a0001c0001t0006 | 3 | NA19066.hp1 NA19086.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*281delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 281 | chr2 | 48687415 | |||||
| chr2:48687476
|
C | G | 4 | a0002c0002t0002a0002c0002t0005a0002c0005t0002others(1): Show | 57 | HG00099.hp2 HG00544.hp2 HG00733.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*221G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 221 | chr2 | 48687476 | |||||
| chr2:48687549
|
A | G | 5 | a0002c0002t0003a0002c0011t0003a0003c0003t0003others(2): Show | 23 | HG01070.hp2 HG01123.hp1 HG01243.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*148T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 148 | chr2 | 48687549 | |||||
| chr2:48687566
|
G | A | 1 | a0002c0002t0005 | 5 | HG02145.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*131C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 131 | chr2 | 48687566 | |||||
| chr2:48687675
|
A | C | 1 | a0001c0001t0007 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*22T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 11/11 | 22 | chr2 | 48687675 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48688962
|
C | T | 18 | a0002c0002t0004g0005a0002c0002t0004g0068a0002c0002t0004g0074others(15): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.948-113G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48688962 | ||||||
| chr2:48689059
|
A | G | 1 | a0002c0002t0001g0082 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.948-210T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689059 | ||||||
| chr2:48689082
|
T | C | 1 | a0001c0012t0001g0023 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.948-233A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689082 | ||||||
| chr2:48689090
|
TATATATA others(11): Show |
T | 2 | a0001c0001t0001g0042a0001c0001t0001g0280 | 2 | HG02074.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.948-259_948-242del others(18): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689090 | ||||||
| chr2:48689172
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.948-323G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689172 | ||||||
| chr2:48689184
|
C | T | 310 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(307): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.948-335G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689184 | ||||||
| chr2:48689185
|
A | G | 12 | a0002c0002t0001g0082a0002c0002t0001g0092a0002c0002t0001g0229others(9): Show | 12 | HG00642.hp2 HG01361.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-336T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689185 | ||||||
| chr2:48689315
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.948-466T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689315 | ||||||
| chr2:48689427
|
G | C | 2 | a0002c0002t0003g0245a0002c0002t0003g0262 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.948-578C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689427 | ||||||
| chr2:48689466
|
A | T | 1 | a0002c0002t0001g0325 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.948-617T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689466 | ||||||
| chr2:48689493
|
C | T | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.948-644G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689493 | ||||||
| chr2:48689676
|
C | T | 1 | a0002c0002t0002g0164 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.948-827G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689676 | ||||||
| chr2:48689683
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.948-834T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689683 | ||||||
| chr2:48689725
|
T | C | 51 | a0002c0002t0002g0009a0002c0002t0002g0020a0002c0002t0002g0038others(48): Show | 52 | HG00099.hp2 HG00544.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.948-876A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689725 | ||||||
| chr2:48689738
|
C | T | 3 | a0001c0001t0001g0163a0002c0002t0002g0150a0003c0003t0002g0354 | 3 | HG00609.hp1 HG01256.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.948-889G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689738 | ||||||
| chr2:48689933
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.948-1084G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689933 | ||||||
| chr2:48689950
|
G | A | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.948-1101C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48689950 | ||||||
| chr2:48690004
|
C | T | 4 | a0001c0001t0001g0117a0001c0001t0001g0255a0001c0001t0001g0279others(1): Show | 4 | HG00741.hp2 NA18998.hp2 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.948-1155G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690004 | ||||||
| chr2:48690005
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0026 | 2 | NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.948-1156C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690005 | ||||||
| chr2:48690037
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.948-1188C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690037 | ||||||
| chr2:48690101
|
G | A | 5 | a0002c0002t0005g0067a0002c0002t0005g0081a0002c0002t0005g0213others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.948-1252C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690101 | ||||||
| chr2:48690158
|
C | G | 1 | a0002c0002t0001g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.948-1309G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690158 | ||||||
| chr2:48690158
|
C | T | 18 | a0002c0002t0004g0005a0002c0002t0004g0068a0002c0002t0004g0074others(15): Show | 20 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.948-1309G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690158 | ||||||
| chr2:48690669
|
G | A | 2 | a0007c0009t0004g0069a0007c0009t0004g0099 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.948-1820C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690669 | ||||||
| chr2:48690689
|
A | G | 1 | a0002c0002t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.948-1840T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690689 | ||||||
| chr2:48690703
|
A | G | 12 | a0002c0002t0001g0082a0002c0002t0001g0092a0002c0002t0001g0229others(9): Show | 12 | HG00642.hp2 HG01361.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.948-1854T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690703 | ||||||
| chr2:48690814
|
C | A | 1 | a0002c0002t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.948-1965G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690814 | ||||||
| chr2:48690884
|
G | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.948-2035C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48690884 | ||||||
| chr2:48691003
|
C | T | 1 | a0002c0002t0002g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.948-2154G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691003 | ||||||
| chr2:48691119
|
T | C | 2 | a0006c0007t0003g0047a0006c0007t0003g0316 | 2 | HG01070.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.948-2270A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691119 | ||||||
| chr2:48691402
|
G | A | 7 | a0002c0002t0002g0087a0002c0002t0002g0147a0002c0002t0002g0155others(4): Show | 7 | HG02129.hp2 NA18948.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.948-2553C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691402 | ||||||
| chr2:48691476
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.948-2627T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691476 | ||||||
| chr2:48691517
|
A | G | 2 | a0001c0001t0001g0301a0001c0001t0001g0321 | 2 | NA18974.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.948-2668T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691517 | ||||||
| chr2:48691574
|
G | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0304 | 2 | HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.947+2650C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691574 | ||||||
| chr2:48691656
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.947+2568C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691656 | ||||||
| chr2:48691769
|
T | C | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.947+2455A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691769 | ||||||
| chr2:48691818
|
C | T | 2 | a0001c0001t0001g0216a0001c0001t0007g0115 | 2 | HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.947+2406G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691818 | ||||||
| chr2:48691845
|
C | CA | 15 | a0001c0001t0001g0049a0001c0001t0001g0086a0001c0001t0001g0101others(12): Show | 15 | HG01081.hp2 HG01099.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.947+2378dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691845 | ||||||
| chr2:48691845
|
CA | C | 30 | a0001c0001t0001g0039a0001c0001t0001g0162a0001c0001t0001g0238others(27): Show | 30 | HG00738.hp2 HG01070.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.947+2378delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691845 | ||||||
| chr2:48691845
|
CAA | C | 16 | a0002c0002t0004g0005a0002c0002t0004g0068a0002c0002t0004g0074others(13): Show | 18 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.947+2377_947+2378d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691845 | ||||||
| chr2:48691845
|
CAAA | C | 31 | a0002c0002t0001g0016a0002c0002t0001g0030a0002c0002t0001g0037others(28): Show | 31 | HG00642.hp2 HG01109.hp1 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.947+2376_947+2378d others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691845 | ||||||
| chr2:48691877
|
C | T | 1 | a0002c0002t0002g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.947+2347G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48691877 | ||||||
| chr2:48692149
|
C | T | 2 | a0002c0002t0002g0200a0002c0002t0002g0311 | 2 | HG02698.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.947+2075G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692149 | ||||||
| chr2:48692270
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.947+1954T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692270 | ||||||
| chr2:48692360
|
T | C | 14 | a0001c0001t0001g0033a0001c0001t0001g0062a0001c0001t0001g0088others(11): Show | 14 | HG00558.hp2 HG00609.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.947+1864A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692360 | ||||||
| chr2:48692458
|
T | C | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.947+1766A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692458 | ||||||
| chr2:48692516
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.947+1708G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692516 | ||||||
| chr2:48692641
|
C | A | 2 | a0001c0001t0001g0125a0001c0001t0006g0126 | 2 | NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.947+1583G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692641 | ||||||
| chr2:48692925
|
A | G | 5 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG02027.hp2 HG02165.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.947+1299T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48692925 | ||||||
| chr2:48693124
|
C | T | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.947+1100G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48693124 | ||||||
| chr2:48693802
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.947+422T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 10/10 | chr2 | 48693802 | ||||||
| chr2:48694572
|
A | G | 2 | a0002c0005t0001g0066a0002c0005t0001g0206 | 2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.867-268T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48694572 | ||||||
| chr2:48694982
|
C | G | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.867-678G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48694982 | ||||||
| chr2:48695038
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.867-734A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695038 | ||||||
| chr2:48695049
|
A | G | 2 | a0002c0002t0001g0139a0002c0002t0001g0204 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.867-745T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695049 | ||||||
| chr2:48695275
|
C | T | 11 | a0001c0001t0001g0008a0001c0001t0001g0134a0001c0001t0001g0135others(8): Show | 12 | NA18944.hp1 NA18952.hp1 NA18962.hp2 others(9): Show |
intron_variant | MODIFIER | c.867-971G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695275 | ||||||
| chr2:48695414
|
T | C | 1 | a0002c0002t0003g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.867-1110A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695414 | ||||||
| chr2:48695422
|
C | T | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(311): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.867-1118G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695422 | ||||||
| chr2:48695445
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.867-1141T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695445 | ||||||
| chr2:48695446
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.867-1142G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695446 | ||||||
| chr2:48695564
|
A | G | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.867-1260T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695564 | ||||||
| chr2:48695884
|
C | G | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.867-1580G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695884 | ||||||
| chr2:48695926
|
T | C | 358 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(355): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.867-1622A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48695926 | ||||||
| chr2:48696015
|
A | C | 17 | a0002c0002t0003g0014a0002c0002t0003g0064a0002c0002t0003g0065others(14): Show | 17 | HG01243.hp1 HG02486.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.867-1711T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696015 | ||||||
| chr2:48696141
|
C | T | 4 | a0001c0001t0001g0173a0001c0001t0001g0187a0001c0001t0001g0220others(1): Show | 4 | HG00438.hp2 NA18947.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.867-1837G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696141 | ||||||
| chr2:48696170
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.867-1866T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696170 | ||||||
| chr2:48696264
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0054others(3): Show | 7 | HG01099.hp2 NA18945.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.867-1960T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696264 | ||||||
| chr2:48696330
|
A | C | 1 | a0002c0002t0002g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.867-2026T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696330 | ||||||
| chr2:48696388
|
A | G | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.867-2084T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696388 | ||||||
| chr2:48696396
|
G | T | 19 | a0002c0002t0001g0234a0002c0002t0004g0005a0002c0002t0004g0068others(16): Show | 21 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.867-2092C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696396 | ||||||
| chr2:48696403
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.867-2099G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696403 | ||||||
| chr2:48696408
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.867-2104G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696408 | ||||||
| chr2:48696483
|
G | T | 5 | a0002c0002t0005g0067a0002c0002t0005g0081a0002c0002t0005g0213others(2): Show | 5 | HG02145.hp1 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.866+2132C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696483 | ||||||
| chr2:48696595
|
A | C | 12 | a0002c0002t0001g0082a0002c0002t0001g0092a0002c0002t0001g0229others(9): Show | 12 | HG00642.hp2 HG01361.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.866+2020T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696595 | ||||||
| chr2:48696687
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.866+1928C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696687 | ||||||
| chr2:48696711
|
T | G | 4 | a0002c0002t0003g0110a0002c0002t0003g0112a0003c0003t0003g0329others(1): Show | 4 | HG01243.hp1 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.866+1904A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696711 | ||||||
| chr2:48696788
|
T | A | 1 | a0002c0002t0001g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.866+1827A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696788 | ||||||
| chr2:48696832
|
C | CA | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(223): Show | 236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.866+1782dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696832 | ||||||
| chr2:48696892
|
C | T | 23 | a0002c0002t0001g0234a0002c0002t0003g0014a0002c0002t0003g0064others(20): Show | 23 | HG01070.hp2 HG01123.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.866+1723G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696892 | ||||||
| chr2:48696909
|
C | A | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.866+1706G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696909 | ||||||
| chr2:48696952
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(319): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.866+1663G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48696952 | ||||||
| chr2:48697063
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.866+1552G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697063 | ||||||
| chr2:48697099
|
C | T | 1 | a0002c0002t0001g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.866+1516G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697099 | ||||||
| chr2:48697174
|
T | G | 358 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(355): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.866+1441A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697174 | ||||||
| chr2:48697337
|
C | T | 321 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(318): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.866+1278G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697337 | ||||||
| chr2:48697682
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0025others(73): Show | 78 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.866+933T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697682 | ||||||
| chr2:48697684
|
T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0096others(3): Show | 7 | HG02015.hp2 HG02056.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.866+931A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697684 | ||||||
| chr2:48697690
|
A | T | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.866+925T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697690 | ||||||
| chr2:48697737
|
C | T | 4 | a0001c0001t0001g0085a0001c0001t0001g0091a0001c0001t0001g0093others(1): Show | 4 | HG01106.hp1 HG01255.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.866+878G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48697737 | ||||||
| chr2:48698012
|
A | G | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.866+603T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698012 | ||||||
| chr2:48698013
|
C | T | 1 | a0004c0004t0001g0328 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.866+602G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698013 | ||||||
| chr2:48698033
|
C | T | 2 | a0002c0002t0001g0139a0002c0002t0001g0204 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.866+582G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698033 | ||||||
| chr2:48698051
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.866+564C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698051 | ||||||
| chr2:48698552
|
C | G | 15 | a0001c0001t0001g0184a0001c0001t0001g0240a0001c0001t0001g0312others(12): Show | 15 | HG00280.hp1 HG00735.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.866+63G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698552 | ||||||
| chr2:48698590
|
G | A | 2 | a0003c0003t0001g0353a0003c0003t0001g0358 | 2 | HG02280.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.866+25C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698590 | ||||||
| chr2:48698597
|
C | G | 1 | a0005c0008t0004g0361 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.866+18G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698597 | ||||||
| chr2:48698607
|
C | T | 242 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0011others(239): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
splice_region_variant&intron_variant | LOW | c.866+8G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 9/10 | chr2 | 48698607 | ||||||
| chr2:48698847
|
AT | A | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(350): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.681-48delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48698847 | ||||||
| chr2:48698993
|
T | C | 8 | a0001c0001t0001g0158a0001c0001t0001g0231a0001c0001t0001g0318others(5): Show | 8 | HG00140.hp2 HG01257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.681-193A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48698993 | ||||||
| chr2:48698999
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.681-199C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48698999 | ||||||
| chr2:48699043
|
G | C | 358 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(355): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.681-243C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699043 | ||||||
| chr2:48699170
|
A | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0259others(2): Show | 6 | HG02015.hp2 HG02056.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.681-370T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699170 | ||||||
| chr2:48699282
|
C | G | 2 | a0001c0001t0001g0263a0002c0002t0001g0234 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.681-482G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699282 | ||||||
| chr2:48699302
|
C | G | 1 | a0001c0001t0001g0321 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.681-502G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699302 | ||||||
| chr2:48699458
|
C | G | 1 | a0005c0008t0004g0361 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.681-658G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699458 | ||||||
| chr2:48699649
|
A | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0233others(21): Show | 28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.681-849T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699649 | ||||||
| chr2:48699664
|
TAATGCAT others(26): Show |
T | 1 | a0001c0006t0001g0151 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.681-897_681-865del others(33): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699664 | ||||||
| chr2:48699873
|
C | T | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.681-1073G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48699873 | ||||||
| chr2:48700024
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.681-1224A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700024 | ||||||
| chr2:48700059
|
C | T | 3 | a0002c0002t0004g0068a0003c0003t0004g0334a0003c0003t0004g0338 | 3 | HG02559.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.681-1259G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700059 | ||||||
| chr2:48700090
|
G | T | 1 | a0002c0002t0002g0167 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.681-1290C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700090 | ||||||
| chr2:48700107
|
A | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0057others(67): Show | 74 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.681-1307T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700107 | ||||||
| chr2:48700136
|
A | G | 1 | a0002c0002t0001g0297 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.681-1336T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700136 | ||||||
| chr2:48700364
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.681-1564C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700364 | ||||||
| chr2:48700556
|
C | T | 8 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0061others(5): Show | 8 | HG00642.hp1 HG02273.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.681-1756G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700556 | ||||||
| chr2:48700568
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.681-1768A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700568 | ||||||
| chr2:48700737
|
AGACCCCT others(35): Show |
A | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.681-1979_681-1938d others(44): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700737 | ||||||
| chr2:48700898
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.681-2098C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48700898 | ||||||
| chr2:48701160
|
T | A | 4 | a0005c0008t0004g0012a0005c0008t0004g0361a0007c0009t0004g0069others(1): Show | 5 | HG02055.hp2 HG03139.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-2360A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701160 | ||||||
| chr2:48701394
|
C | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0001g0057others(66): Show | 73 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.681-2594G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701394 | ||||||
| chr2:48701460
|
T | C | 1 | a0004c0004t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.681-2660A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701460 | ||||||
| chr2:48701503
|
A | G | 54 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0028others(51): Show | 55 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.681-2703T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701503 | ||||||
| chr2:48701544
|
A | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0233others(21): Show | 28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.681-2744T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48701544 | ||||||
| chr2:48702010
|
T | G | 2 | a0003c0003t0002g0346a0003c0003t0002g0347 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.681-3210A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702010 | ||||||
| chr2:48702053
|
C | T | 1 | a0002c0002t0002g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.681-3253G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702053 | ||||||
| chr2:48702063
|
AG | A | 15 | a0001c0001t0001g0111a0001c0001t0001g0129a0002c0002t0001g0139others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.681-3264delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702063 | ||||||
| chr2:48702068
|
G | A | 40 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(37): Show | 40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.681-3268C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702068 | ||||||
| chr2:48702263
|
C | CT | 24 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0233others(21): Show | 28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.681-3464dupA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702263 | ||||||
| chr2:48702263
|
CT | C | 48 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0103others(45): Show | 48 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.681-3464delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702263 | ||||||
| chr2:48702277
|
T | A | 1 | a0002c0002t0002g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.681-3477A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702277 | ||||||
| chr2:48702282
|
A | G | 4 | a0001c0001t0001g0207a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG01358.hp1 HG02970.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.681-3482T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702282 | ||||||
| chr2:48702327
|
A | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.681-3527T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702327 | ||||||
| chr2:48702357
|
G | A | 40 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(37): Show | 40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.681-3557C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702357 | ||||||
| chr2:48702406
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.681-3606G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702406 | ||||||
| chr2:48702407
|
T | C | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.681-3607A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702407 | ||||||
| chr2:48702408
|
C | A | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.681-3608G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702408 | ||||||
| chr2:48702424
|
C | T | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.681-3624G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702424 | ||||||
| chr2:48702425
|
G | C | 96 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0052others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.681-3625C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702425 | ||||||
| chr2:48702453
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(36): Show | 41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.681-3653G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702453 | ||||||
| chr2:48702639
|
C | T | 3 | a0001c0001t0001g0118a0001c0006t0001g0225a0002c0002t0002g0200 | 3 | HG02300.hp1 HG02602.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.681-3839G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702639 | ||||||
| chr2:48702798
|
C | T | 1 | a0004c0004t0001g0345 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.681-3998G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702798 | ||||||
| chr2:48702807
|
A | T | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.681-4007T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702807 | ||||||
| chr2:48702821
|
G | A | 1 | a0002c0010t0001g0212 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.681-4021C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702821 | ||||||
| chr2:48702929
|
A | G | 2 | a0002c0002t0001g0139a0002c0002t0001g0204 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.681-4129T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48702929 | ||||||
| chr2:48703015
|
A | G | 1 | a0002c0002t0002g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.681-4215T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703015 | ||||||
| chr2:48703074
|
T | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0233others(22): Show | 29 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.681-4274A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703074 | ||||||
| chr2:48703113
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.681-4313C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703113 | ||||||
| chr2:48703224
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0233others(21): Show | 28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.681-4424C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703224 | ||||||
| chr2:48703429
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.681-4629G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703429 | ||||||
| chr2:48703551
|
C | G | 3 | a0001c0001t0001g0263a0002c0002t0001g0234a0002c0002t0003g0245 | 3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.681-4751G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703551 | ||||||
| chr2:48703681
|
C | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.681-4881G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703681 | ||||||
| chr2:48703752
|
C | T | 5 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0247others(2): Show | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-4952G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703752 | ||||||
| chr2:48703753
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.681-4953C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703753 | ||||||
| chr2:48703864
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.681-5064T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703864 | ||||||
| chr2:48703889
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0259others(2): Show | 6 | HG02015.hp2 HG02056.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.680+5059G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703889 | ||||||
| chr2:48703907
|
A | G | 4 | a0001c0001t0001g0057a0001c0001t0001g0327a0002c0002t0002g0161others(1): Show | 4 | HG01361.hp2 HG02735.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+5041T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703907 | ||||||
| chr2:48703915
|
C | A | 1 | a0004c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.680+5033G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48703915 | ||||||
| chr2:48704169
|
C | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0233others(21): Show | 28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.680+4779G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704169 | ||||||
| chr2:48704211
|
A | G | 1 | a0004c0004t0001g0356 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.680+4737T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704211 | ||||||
| chr2:48704261
|
C | T | 2 | a0001c0001t0001g0207a0002c0002t0003g0262 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.680+4687G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704261 | ||||||
| chr2:48704301
|
T | C | 24 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0233others(21): Show | 28 | HG01361.hp1 HG01433.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.680+4647A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704301 | ||||||
| chr2:48704317
|
C | T | 9 | a0001c0001t0001g0075a0002c0002t0001g0016a0002c0002t0001g0030others(6): Show | 9 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.680+4631G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704317 | ||||||
| chr2:48704318
|
G | A | 1 | a0002c0002t0001g0297 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.680+4630C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704318 | ||||||
| chr2:48704470
|
G | C | 1 | a0001c0001t0001g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.680+4478C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704470 | ||||||
| chr2:48704518
|
C | A | 29 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0104others(26): Show | 29 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.680+4430G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704518 | ||||||
| chr2:48704571
|
G | GTTATTGG others(126): Show |
1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.680+4244_680+4376d others(135): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704571 | ||||||
| chr2:48704599
|
C | A | 1 | a0001c0001t0001g0230 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.680+4349G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704599 | ||||||
| chr2:48704662
|
C | G | 1 | a0002c0002t0002g0317 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.680+4286G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48704662 | ||||||
| chr2:48705037
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.680+3911T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705037 | ||||||
| chr2:48705083
|
C | T | 3 | a0002c0002t0005g0067a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3865G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705083 | ||||||
| chr2:48705084
|
A | G | 3 | a0002c0002t0005g0067a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3864T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705084 | ||||||
| chr2:48705087
|
A | G | 3 | a0002c0002t0005g0067a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3861T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705087 | ||||||
| chr2:48705130
|
C | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0199others(4): Show | 8 | HG00558.hp2 HG02015.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.680+3818G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705130 | ||||||
| chr2:48705245
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0032a0001c0001t0001g0041others(1): Show | 4 | HG00558.hp1 HG02027.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+3703C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705245 | ||||||
| chr2:48705408
|
T | G | 3 | a0002c0002t0005g0067a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3540A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705408 | ||||||
| chr2:48705506
|
T | G | 1 | a0002c0002t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.680+3442A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705506 | ||||||
| chr2:48705539
|
T | G | 3 | a0002c0002t0005g0067a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+3409A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705539 | ||||||
| chr2:48705590
|
T | A | 1 | a0001c0001t0001g0277 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.680+3358A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705590 | ||||||
| chr2:48705793
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0221 | 2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.680+3155T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705793 | ||||||
| chr2:48705806
|
C | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(37): Show | 42 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.680+3142G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705806 | ||||||
| chr2:48705809
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.680+3139G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705809 | ||||||
| chr2:48705952
|
A | G | 3 | a0002c0002t0005g0067a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+2996T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705952 | ||||||
| chr2:48705957
|
G | A | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.680+2991C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48705957 | ||||||
| chr2:48706289
|
G | A | 3 | a0001c0001t0001g0263a0002c0002t0001g0234a0002c0002t0003g0245 | 3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+2659C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706289 | ||||||
| chr2:48706354
|
A | G | 1 | a0002c0002t0003g0245 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.680+2594T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706354 | ||||||
| chr2:48706384
|
C | T | 334 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(331): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.680+2564G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706384 | ||||||
| chr2:48706412
|
C | T | 26 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0104others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.680+2536G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706412 | ||||||
| chr2:48706534
|
C | T | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.680+2414G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706534 | ||||||
| chr2:48706665
|
T | C | 5 | a0001c0001t0001g0287a0003c0003t0002g0346a0003c0003t0002g0347others(2): Show | 5 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+2283A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706665 | ||||||
| chr2:48706705
|
C | T | 32 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0104others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.680+2243G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706705 | ||||||
| chr2:48706737
|
G | A | 226 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(223): Show | 233 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.680+2211C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706737 | ||||||
| chr2:48706751
|
G | A | 26 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0104others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.680+2197C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706751 | ||||||
| chr2:48706762
|
C | T | 21 | a0001c0001t0001g0111a0001c0001t0001g0129a0001c0001t0001g0292others(18): Show | 21 | HG00738.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.680+2186G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706762 | ||||||
| chr2:48706788
|
C | T | 40 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(37): Show | 40 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.680+2160G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706788 | ||||||
| chr2:48706814
|
C | G | 2 | a0002c0002t0002g0310a0003c0003t0002g0354 | 2 | HG01081.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.680+2134G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706814 | ||||||
| chr2:48706873
|
C | G | 20 | a0001c0001t0001g0111a0001c0001t0001g0129a0002c0002t0001g0139others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.680+2075G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706873 | ||||||
| chr2:48706895
|
G | A | 32 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0104others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.680+2053C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706895 | ||||||
| chr2:48706906
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.680+2042A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706906 | ||||||
| chr2:48706967
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0121a0001c0001t0001g0301 | 3 | HG00438.hp1 NA18974.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.680+1981G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48706967 | ||||||
| chr2:48707069
|
G | A | 3 | a0002c0002t0005g0067a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02145.hp1 HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.680+1879C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707069 | ||||||
| chr2:48707192
|
G | A | 39 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(36): Show | 39 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.680+1756C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707192 | ||||||
| chr2:48707196
|
T | C | 357 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(354): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.680+1752A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707196 | ||||||
| chr2:48707196
|
T | G | 1 | a0001c0001t0001g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.680+1752A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707196 | ||||||
| chr2:48707245
|
C | G | 3 | a0001c0001t0001g0263a0002c0002t0001g0234a0002c0002t0003g0245 | 3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+1703G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707245 | ||||||
| chr2:48707280
|
G | A | 3 | a0001c0001t0001g0263a0002c0002t0001g0234a0002c0002t0003g0245 | 3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.680+1668C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707280 | ||||||
| chr2:48707317
|
T | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0125a0001c0001t0006g0126 | 3 | HG02074.hp2 NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.680+1631A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707317 | ||||||
| chr2:48707342
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.680+1606C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707342 | ||||||
| chr2:48707400
|
C | G | 1 | a0001c0001t0001g0319 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.680+1548G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707400 | ||||||
| chr2:48707420
|
CTG | C | 33 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0104others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.680+1526_680+1527d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707420 | ||||||
| chr2:48707484
|
T | C | 73 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0052others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.680+1464A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707484 | ||||||
| chr2:48707490
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.680+1458G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707490 | ||||||
| chr2:48707683
|
T | C | 5 | a0001c0001t0001g0240a0001c0001t0001g0314a0002c0002t0002g0109others(2): Show | 5 | HG00280.hp1 HG01981.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.680+1265A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707683 | ||||||
| chr2:48707733
|
A | G | 2 | a0001c0001t0001g0207a0002c0002t0003g0262 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.680+1215T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707733 | ||||||
| chr2:48707995
|
G | A | 2 | a0002c0005t0001g0066a0002c0011t0003g0249 | 2 | HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.680+953C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48707995 | ||||||
| chr2:48708002
|
C | G | 22 | a0001c0001t0001g0111a0001c0001t0001g0129a0001c0001t0001g0292others(19): Show | 22 | HG00738.hp1 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.680+946G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708002 | ||||||
| chr2:48708050
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.680+898G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708050 | ||||||
| chr2:48708071
|
C | T | 73 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0052others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.680+877G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708071 | ||||||
| chr2:48708092
|
C | A | 73 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0052others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.680+856G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708092 | ||||||
| chr2:48708109
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.680+839C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708109 | ||||||
| chr2:48708152
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 5 | HG01123.hp2 HG01192.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.680+796C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708152 | ||||||
| chr2:48708181
|
T | G | 1 | a0002c0002t0002g0157 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.680+767A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708181 | ||||||
| chr2:48708187
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.680+761G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708187 | ||||||
| chr2:48708253
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 296 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(293): Show |
intron_variant | MODIFIER | c.680+695G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708253 | ||||||
| chr2:48708475
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.680+473C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708475 | ||||||
| chr2:48708484
|
A | C | 1 | a0001c0001t0001g0304 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.680+464T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708484 | ||||||
| chr2:48708548
|
CCA | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(49): Show | 54 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.680+398_680+399del others(2): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708548 | ||||||
| chr2:48708548
|
CCACA | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(299): Show | 313 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.680+396_680+399del others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708548 | ||||||
| chr2:48708548
|
CCACACA | C | 4 | a0002c0002t0001g0297a0002c0002t0005g0067a0002c0002t0005g0250others(1): Show | 4 | HG02145.hp1 HG02451.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.680+394_680+399del others(6): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708548 | ||||||
| chr2:48708668
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.680+280G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708668 | ||||||
| chr2:48708710
|
C | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0111others(43): Show | 50 | HG00738.hp1 HG01243.hp1 HG01361.hp1 others(47): Show |
intron_variant | MODIFIER | c.680+238G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708710 | ||||||
| chr2:48708791
|
T | C | 50 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0042others(47): Show | 51 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.680+157A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708791 | ||||||
| chr2:48708828
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0006g0126 | 2 | NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.680+120G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708828 | ||||||
| chr2:48708867
|
G | A | 32 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0104others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.680+81C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708867 | ||||||
| chr2:48708876
|
G | A | 1 | a0002c0002t0003g0170 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.680+72C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 8/10 | chr2 | 48708876 | ||||||
| chr2:48709290
|
C | T | 3 | a0002c0002t0003g0171a0002c0002t0003g0293a0002c0011t0003g0249 | 3 | HG02723.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.606-268G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709290 | ||||||
| chr2:48709291
|
C | G | 1 | a0002c0002t0005g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.606-269G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709291 | ||||||
| chr2:48709312
|
A | G | 9 | a0001c0001t0001g0011a0001c0001t0001g0096a0001c0001t0001g0199others(6): Show | 10 | HG00558.hp2 HG02015.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.606-290T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709312 | ||||||
| chr2:48709320
|
A | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.606-298T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709320 | ||||||
| chr2:48709450
|
T | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(153): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.606-428A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709450 | ||||||
| chr2:48709453
|
T | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(153): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.606-431A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709453 | ||||||
| chr2:48709621
|
C | T | 5 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0247others(2): Show | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.606-599G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709621 | ||||||
| chr2:48709720
|
AG | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0267others(8): Show | 11 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.606-699delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709720 | ||||||
| chr2:48709778
|
ATCTGG | A | 3 | a0001c0001t0001g0254a0001c0001t0001g0264a0002c0002t0002g0324 | 3 | HG03654.hp2 HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.606-761_606-757del others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709778 | ||||||
| chr2:48709794
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.606-772G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709794 | ||||||
| chr2:48709944
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.606-922C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709944 | ||||||
| chr2:48709945
|
C | A | 1 | a0001c0001t0001g0032 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.606-923G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709945 | ||||||
| chr2:48709974
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.606-952C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48709974 | ||||||
| chr2:48710015
|
C | T | 47 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0042others(44): Show | 48 | HG00423.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.606-993G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710015 | ||||||
| chr2:48710084
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0006g0126 | 2 | NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.606-1062A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710084 | ||||||
| chr2:48710210
|
G | A | 76 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.606-1188C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710210 | ||||||
| chr2:48710329
|
A | G | 1 | a0002c0002t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.606-1307T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710329 | ||||||
| chr2:48710437
|
G | A | 24 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0117others(21): Show | 24 | HG00140.hp1 HG00639.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.606-1415C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710437 | ||||||
| chr2:48710475
|
C | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(131): Show | 140 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.606-1453G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710475 | ||||||
| chr2:48710632
|
A | C | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.606-1610T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710632 | ||||||
| chr2:48710638
|
C | G | 3 | a0001c0001t0001g0263a0002c0002t0001g0234a0002c0002t0003g0245 | 3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.606-1616G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710638 | ||||||
| chr2:48710684
|
T | G | 67 | a0001c0001t0001g0027a0001c0001t0001g0039a0001c0001t0001g0052others(64): Show | 67 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.606-1662A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710684 | ||||||
| chr2:48710773
|
T | C | 1 | a0004c0004t0001g0344 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.606-1751A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710773 | ||||||
| chr2:48710800
|
G | T | 15 | a0001c0001t0001g0111a0001c0001t0001g0129a0002c0002t0001g0139others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.606-1778C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710800 | ||||||
| chr2:48710844
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.606-1822C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710844 | ||||||
| chr2:48710901
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.606-1879G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710901 | ||||||
| chr2:48710989
|
C | A | 1 | a0001c0001t0001g0306 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.606-1967G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48710989 | ||||||
| chr2:48711116
|
G | A | 5 | a0001c0001t0001g0287a0003c0003t0002g0346a0003c0003t0002g0347others(2): Show | 5 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.606-2094C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711116 | ||||||
| chr2:48711202
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(177): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.606-2180T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711202 | ||||||
| chr2:48711217
|
C | T | 202 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0011others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.606-2195G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711217 | ||||||
| chr2:48711218
|
G | T | 2 | a0002c0002t0002g0310a0003c0003t0002g0354 | 2 | HG01081.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.606-2196C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711218 | ||||||
| chr2:48711221
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0001g0269 | 2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.606-2199G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711221 | ||||||
| chr2:48711523
|
C | T | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(234): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.605+2463G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711523 | ||||||
| chr2:48711552
|
C | T | 210 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(207): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.605+2434G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711552 | ||||||
| chr2:48711554
|
T | G | 82 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(79): Show | 86 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.605+2432A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711554 | ||||||
| chr2:48711582
|
T | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 165 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.605+2404A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711582 | ||||||
| chr2:48711654
|
T | C | 167 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(164): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.605+2332A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711654 | ||||||
| chr2:48711699
|
C | T | 41 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(38): Show | 43 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.605+2287G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711699 | ||||||
| chr2:48711768
|
A | C | 1 | a0001c0001t0001g0182 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.605+2218T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711768 | ||||||
| chr2:48711957
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(185): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.605+2029T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711957 | ||||||
| chr2:48711994
|
G | A | 1 | a0002c0002t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.605+1992C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48711994 | ||||||
| chr2:48712038
|
A | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.605+1948T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712038 | ||||||
| chr2:48712282
|
G | T | 1 | a0002c0002t0003g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.605+1704C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712282 | ||||||
| chr2:48712407
|
A | G | 6 | a0002c0002t0001g0082a0002c0002t0001g0229a0003c0003t0001g0330others(3): Show | 6 | HG01361.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.605+1579T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712407 | ||||||
| chr2:48712413
|
G | A | 72 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(69): Show | 74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.605+1573C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712413 | ||||||
| chr2:48712418
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.605+1568G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712418 | ||||||
| chr2:48712506
|
G | A | 3 | a0001c0001t0001g0207a0002c0002t0001g0246a0002c0002t0003g0262 | 3 | HG02970.hp2 HG04204.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.605+1480C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712506 | ||||||
| chr2:48712560
|
C | T | 1 | a0004c0004t0001g0333 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.605+1426G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712560 | ||||||
| chr2:48712571
|
C | G | 1 | a0002c0002t0005g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.605+1415G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712571 | ||||||
| chr2:48712589
|
T | G | 2 | a0002c0002t0002g0273a0002c0005t0002g0144 | 2 | NA18995.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.605+1397A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712589 | ||||||
| chr2:48712590
|
A | T | 72 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(69): Show | 74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.605+1396T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712590 | ||||||
| chr2:48712603
|
A | G | 55 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0156others(52): Show | 55 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.605+1383T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712603 | ||||||
| chr2:48712723
|
C | G | 72 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(69): Show | 74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.605+1263G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712723 | ||||||
| chr2:48712781
|
T | C | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.605+1205A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712781 | ||||||
| chr2:48712814
|
T | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0015others(51): Show | 56 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.605+1172A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712814 | ||||||
| chr2:48712858
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.605+1128T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712858 | ||||||
| chr2:48712934
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0071others(46): Show | 52 | HG00099.hp2 HG00738.hp1 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.605+1052T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48712934 | ||||||
| chr2:48713007
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.605+979G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713007 | ||||||
| chr2:48713016
|
G | A | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.605+970C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713016 | ||||||
| chr2:48713074
|
A | T | 2 | a0002c0002t0002g0322a0002c0002t0002g0323 | 2 | HG00735.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.605+912T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713074 | ||||||
| chr2:48713083
|
G | A | 2 | a0002c0002t0002g0268a0002c0002t0002g0281 | 2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.605+903C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713083 | ||||||
| chr2:48713161
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 152 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.605+825G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713161 | ||||||
| chr2:48713227
|
AAG | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(283): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.605+757_605+758del others(2): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713227 | ||||||
| chr2:48713229
|
G | C | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.605+757C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713229 | ||||||
| chr2:48713231
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.605+755G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713231 | ||||||
| chr2:48713449
|
G | A | 5 | a0002c0002t0001g0209a0002c0002t0001g0244a0002c0002t0001g0247others(2): Show | 5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.605+537C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713449 | ||||||
| chr2:48713476
|
A | T | 1 | a0001c0001t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.605+510T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713476 | ||||||
| chr2:48713478
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.605+508G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713478 | ||||||
| chr2:48713490
|
A | C | 20 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0172others(17): Show | 20 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.605+496T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713490 | ||||||
| chr2:48713494
|
T | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.605+492A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713494 | ||||||
| chr2:48713510
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.605+476T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713510 | ||||||
| chr2:48713511
|
G | A | 12 | a0001c0001t0001g0075a0002c0002t0001g0016a0002c0002t0001g0030others(9): Show | 12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.605+475C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713511 | ||||||
| chr2:48713541
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(243): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.605+445G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713541 | ||||||
| chr2:48713933
|
CA | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(69): Show | 74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.605+52delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713933 | ||||||
| chr2:48713940
|
A | G | 2 | a0001c0001t0001g0203a0001c0001t0009g0217 | 2 | HG01952.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.605+46T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713940 | ||||||
| chr2:48713948
|
T | C | 1 | a0002c0002t0001g0315 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.605+38A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 7/10 | chr2 | 48713948 | ||||||
| chr2:48714163
|
A | G | 2 | a0002c0002t0002g0310a0003c0003t0002g0354 | 2 | HG01081.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.537-109T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714163 | ||||||
| chr2:48714270
|
A | T | 3 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0318 | 3 | HG00423.hp1 HG02523.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.537-216T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714270 | ||||||
| chr2:48714275
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.537-221G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714275 | ||||||
| chr2:48714289
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.537-235G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714289 | ||||||
| chr2:48714397
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.537-343G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714397 | ||||||
| chr2:48714416
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.537-362C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714416 | ||||||
| chr2:48714422
|
G | A | 3 | a0001c0001t0001g0299a0001c0001t0001g0300a0001c0001t0001g0318 | 3 | HG00423.hp1 HG02523.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.537-368C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714422 | ||||||
| chr2:48714425
|
T | C | 98 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(95): Show | 103 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.537-371A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714425 | ||||||
| chr2:48714483
|
CTT | C | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-431_537-430del others(2): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714483 | ||||||
| chr2:48714483
|
CTTT | C | 16 | a0001c0001t0001g0007a0001c0001t0001g0053a0001c0001t0001g0055others(13): Show | 17 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.537-432_537-430del others(3): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714483 | ||||||
| chr2:48714675
|
A | G | 1 | a0002c0002t0003g0293 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.537-621T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714675 | ||||||
| chr2:48714740
|
T | TAC | 72 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(69): Show | 74 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.537-688_537-687dup others(2): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714740 | ||||||
| chr2:48714771
|
G | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.537-717C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714771 | ||||||
| chr2:48714897
|
G | A | 1 | a0004c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.537-843C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714897 | ||||||
| chr2:48714935
|
T | G | 1 | a0002c0002t0003g0245 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.537-881A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48714935 | ||||||
| chr2:48715143
|
T | A | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(284): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.537-1089A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715143 | ||||||
| chr2:48715386
|
G | A | 1 | a0002c0002t0004g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.537-1332C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715386 | ||||||
| chr2:48715544
|
G | T | 2 | a0002c0002t0003g0128a0002c0002t0003g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.537-1490C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715544 | ||||||
| chr2:48715609
|
T | A | 6 | a0002c0002t0001g0082a0002c0002t0001g0229a0003c0003t0001g0330others(3): Show | 6 | HG01361.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.537-1555A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715609 | ||||||
| chr2:48715623
|
T | A | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.537-1569A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715623 | ||||||
| chr2:48715868
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0045a0006c0007t0003g0047 | 3 | HG00099.hp1 HG01123.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.537-1814G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48715868 | ||||||
| chr2:48716002
|
G | T | 3 | a0002c0002t0001g0082a0003c0003t0001g0330a0003c0003t0001g0357 | 3 | HG01361.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.537-1948C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716002 | ||||||
| chr2:48716056
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.537-2002C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716056 | ||||||
| chr2:48716252
|
G | C | 2 | a0001c0001t0001g0231a0002c0002t0001g0315 | 2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.537-2198C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716252 | ||||||
| chr2:48716657
|
T | C | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.537-2603A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716657 | ||||||
| chr2:48716661
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.537-2607G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716661 | ||||||
| chr2:48716664
|
A | G | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(96): Show | 104 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.537-2610T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716664 | ||||||
| chr2:48716701
|
A | C | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.537-2647T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716701 | ||||||
| chr2:48716948
|
T | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0321 | 2 | HG00280.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.537-2894A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716948 | ||||||
| chr2:48716948
|
T | C | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.537-2894A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716948 | ||||||
| chr2:48716951
|
A | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.537-2897T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48716951 | ||||||
| chr2:48717035
|
T | C | 1 | a0002c0002t0004g0078 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.537-2981A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717035 | ||||||
| chr2:48717048
|
C | T | 3 | a0002c0002t0001g0234a0002c0002t0004g0232a0002c0002t0004g0294 | 3 | HG02622.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.537-2994G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717048 | ||||||
| chr2:48717122
|
C | G | 99 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(96): Show | 104 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.537-3068G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717122 | ||||||
| chr2:48717135
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3081C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717135 | ||||||
| chr2:48717197
|
A | G | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.537-3143T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717197 | ||||||
| chr2:48717206
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.537-3152A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717206 | ||||||
| chr2:48717302
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3248C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717302 | ||||||
| chr2:48717303
|
G | A | 1 | a0004c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.537-3249C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717303 | ||||||
| chr2:48717394
|
A | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3340T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717394 | ||||||
| chr2:48717407
|
C | G | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3353G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717407 | ||||||
| chr2:48717431
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(122): Show | 127 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.537-3377C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717431 | ||||||
| chr2:48717474
|
A | G | 1 | a0002c0002t0001g0030 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.537-3420T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717474 | ||||||
| chr2:48717475
|
A | C | 2 | a0001c0001t0001g0265a0001c0001t0001g0266 | 2 | HG01358.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.537-3421T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717475 | ||||||
| chr2:48717486
|
T | C | 1 | a0002c0002t0002g0043 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.537-3432A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717486 | ||||||
| chr2:48717542
|
C | CTTA | 54 | a0001c0001t0001g0039a0001c0001t0001g0075a0001c0001t0001g0156others(51): Show | 54 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.537-3491_537-3489d others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | ||||||
| chr2:48717542
|
C | CTTATTAT others(5): Show |
47 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(44): Show | 49 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.537-3500_537-3489d others(14): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | ||||||
| chr2:48717542
|
C | CTTATTAT others(8): Show |
13 | a0001c0001t0001g0101a0001c0001t0001g0188a0001c0001t0001g0207others(10): Show | 13 | HG02080.hp1 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.537-3503_537-3489d others(17): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | ||||||
| chr2:48717542
|
C | CTTATTAT others(11): Show |
8 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0172others(5): Show | 8 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.537-3506_537-3489d others(20): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | ||||||
| chr2:48717542
|
C | CTTATTAT others(14): Show |
2 | a0002c0002t0003g0170a0002c0002t0003g0293 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.537-3489_537-3488i others(23): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | ||||||
| chr2:48717542
|
C | CTTATTAT others(20): Show |
1 | a0001c0001t0001g0267 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.537-3489_537-3488i others(29): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717542 | ||||||
| chr2:48717605
|
C | G | 274 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(271): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.537-3551G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717605 | ||||||
| chr2:48717833
|
C | CT | 6 | a0001c0001t0001g0122a0002c0002t0001g0234a0002c0002t0002g0087others(3): Show | 6 | HG02132.hp1 HG02622.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.537-3780dupA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717833 | ||||||
| chr2:48717833
|
CT | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(214): Show | 225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.537-3780delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717833 | ||||||
| chr2:48717833
|
CTT | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0063others(46): Show | 52 | HG00099.hp2 HG01099.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.537-3781_537-3780d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717833 | ||||||
| chr2:48717857
|
C | T | 2 | a0002c0002t0004g0232a0002c0002t0004g0294 | 2 | HG02622.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.537-3803G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717857 | ||||||
| chr2:48717875
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-3821C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48717875 | ||||||
| chr2:48718008
|
C | T | 20 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0172others(17): Show | 20 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.537-3954G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718008 | ||||||
| chr2:48718073
|
A | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0130 | 2 | HG01261.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.537-4019T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718073 | ||||||
| chr2:48718194
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.537-4140C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718194 | ||||||
| chr2:48718346
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0071others(37): Show | 43 | HG00099.hp2 HG01099.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.537-4292G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718346 | ||||||
| chr2:48718611
|
AT | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(67): Show | 72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.537-4558delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718611 | ||||||
| chr2:48718633
|
A | T | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(97): Show | 105 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.537-4579T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718633 | ||||||
| chr2:48718703
|
C | T | 1 | a0002c0002t0008g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.537-4649G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718703 | ||||||
| chr2:48718735
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(67): Show | 72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.537-4681G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718735 | ||||||
| chr2:48718765
|
C | T | 70 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(67): Show | 72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.536+4691G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718765 | ||||||
| chr2:48718815
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(67): Show | 72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.536+4641C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48718815 | ||||||
| chr2:48719028
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(102): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.536+4428T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719028 | ||||||
| chr2:48719055
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.536+4401C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719055 | ||||||
| chr2:48719061
|
G | A | 2 | a0002c0002t0003g0128a0002c0002t0003g0208 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.536+4395C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719061 | ||||||
| chr2:48719091
|
G | A | 1 | a0002c0002t0001g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.536+4365C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719091 | ||||||
| chr2:48719093
|
C | T | 2 | a0002c0002t0002g0273a0002c0005t0002g0144 | 2 | NA18995.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.536+4363G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719093 | ||||||
| chr2:48719094
|
G | A | 33 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0028others(30): Show | 34 | HG00423.hp1 HG00558.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.536+4362C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719094 | ||||||
| chr2:48719118
|
C | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.536+4338G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719118 | ||||||
| chr2:48719195
|
G | A | 1 | a0004c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.536+4261C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719195 | ||||||
| chr2:48719500
|
C | G | 1 | a0003c0003t0003g0348 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.536+3956G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719500 | ||||||
| chr2:48719564
|
C | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | NA18960.hp2 NA19000.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.536+3892G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719564 | ||||||
| chr2:48719579
|
G | C | 1 | a0003c0003t0003g0348 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.536+3877C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719579 | ||||||
| chr2:48719585
|
T | C | 100 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(97): Show | 105 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.536+3871A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719585 | ||||||
| chr2:48719651
|
T | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0063a0002c0002t0001g0072others(9): Show | 15 | HG01433.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.536+3805A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719651 | ||||||
| chr2:48719741
|
G | C | 4 | a0001c0001t0001g0129a0002c0002t0001g0261a0002c0002t0001g0284others(1): Show | 4 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.536+3715C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719741 | ||||||
| chr2:48719749
|
T | G | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.536+3707A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719749 | ||||||
| chr2:48719767
|
G | C | 1 | a0001c0006t0001g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.536+3689C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48719767 | ||||||
| chr2:48720063
|
C | T | 3 | a0002c0002t0001g0234a0002c0002t0004g0232a0002c0002t0004g0294 | 3 | HG02622.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.536+3393G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720063 | ||||||
| chr2:48720103
|
C | A | 1 | a0002c0002t0002g0191 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.536+3353G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720103 | ||||||
| chr2:48720197
|
C | G | 1 | a0002c0002t0001g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.536+3259G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720197 | ||||||
| chr2:48720207
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.536+3249T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720207 | ||||||
| chr2:48720441
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(67): Show | 72 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.536+3015C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720441 | ||||||
| chr2:48720491
|
A | T | 1 | a0002c0002t0002g0307 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.536+2965T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720491 | ||||||
| chr2:48720500
|
T | C | 1 | a0002c0002t0001g0248 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.536+2956A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720500 | ||||||
| chr2:48720533
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.536+2923A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720533 | ||||||
| chr2:48720611
|
A | T | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.536+2845T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720611 | ||||||
| chr2:48720863
|
G | C | 1 | a0002c0002t0003g0064 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.536+2593C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720863 | ||||||
| chr2:48720911
|
G | A | 9 | a0001c0001t0001g0117a0001c0001t0001g0154a0001c0001t0001g0172others(6): Show | 9 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.536+2545C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48720911 | ||||||
| chr2:48721055
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.536+2401A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721055 | ||||||
| chr2:48721196
|
T | G | 1 | a0001c0012t0001g0023 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.536+2260A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721196 | ||||||
| chr2:48721298
|
C | G | 8 | a0001c0001t0001g0104a0001c0001t0001g0105a0002c0002t0002g0237others(5): Show | 8 | HG00099.hp2 HG01099.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.536+2158G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721298 | ||||||
| chr2:48721568
|
A | C | 87 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(84): Show | 91 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.536+1888T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721568 | ||||||
| chr2:48721609
|
C | T | 6 | a0002c0002t0003g0064a0002c0002t0003g0128a0002c0002t0003g0208others(3): Show | 6 | HG02258.hp1 HG02622.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.536+1847G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721609 | ||||||
| chr2:48721663
|
T | C | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.536+1793A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721663 | ||||||
| chr2:48721717
|
A | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.536+1739T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721717 | ||||||
| chr2:48721742
|
T | C | 1 | a0002c0002t0002g0237 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.536+1714A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721742 | ||||||
| chr2:48721839
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0134a0001c0001t0001g0135others(7): Show | 11 | NA18944.hp1 NA18952.hp1 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.536+1617C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721839 | ||||||
| chr2:48721929
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0186a0001c0001t0001g0282others(1): Show | 4 | HG00673.hp1 HG02071.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.536+1527C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721929 | ||||||
| chr2:48721997
|
A | C | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.536+1459T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48721997 | ||||||
| chr2:48722534
|
T | G | 101 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(98): Show | 106 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.536+922A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722534 | ||||||
| chr2:48722539
|
G | A | 1 | a0002c0002t0003g0245 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.536+917C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722539 | ||||||
| chr2:48722788
|
T | C | 5 | a0001c0001t0001g0233a0002c0002t0003g0065a0003c0003t0003g0329others(2): Show | 5 | HG01243.hp2 HG02572.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.536+668A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722788 | ||||||
| chr2:48722893
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.536+563G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722893 | ||||||
| chr2:48722902
|
T | C | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.536+554A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722902 | ||||||
| chr2:48722905
|
C | T | 40 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0071others(37): Show | 43 | HG00099.hp2 HG01099.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.536+551G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722905 | ||||||
| chr2:48722936
|
T | G | 41 | a0001c0001t0001g0039a0001c0001t0001g0156a0001c0001t0001g0190others(38): Show | 41 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.536+520A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48722936 | ||||||
| chr2:48723099
|
A | C | 1 | a0002c0002t0002g0222 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.536+357T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48723099 | ||||||
| chr2:48723169
|
AG | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0134a0001c0001t0001g0135others(7): Show | 11 | NA18944.hp1 NA18952.hp1 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.536+286delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48723169 | ||||||
| chr2:48723263
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.536+193C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48723263 | ||||||
| chr2:48723316
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.536+140G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 6/10 | chr2 | 48723316 | ||||||
| chr2:48724056
|
C | G | 4 | a0001c0001t0001g0142a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | NA18960.hp2 NA19000.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.384-360G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724056 | ||||||
| chr2:48724352
|
G | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0017others(68): Show | 73 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.384-656C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724352 | ||||||
| chr2:48724816
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0052a0004c0004t0001g0333others(1): Show | 4 | HG00639.hp2 HG01109.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+860A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724816 | ||||||
| chr2:48724832
|
G | C | 96 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(93): Show | 101 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.383+844C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724832 | ||||||
| chr2:48724870
|
G | A | 1 | a0002c0002t0002g0311 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.383+806C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724870 | ||||||
| chr2:48724934
|
G | T | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.383+742C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48724934 | ||||||
| chr2:48725064
|
A | G | 1 | a0002c0002t0002g0322 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.383+612T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725064 | ||||||
| chr2:48725310
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.383+366T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725310 | ||||||
| chr2:48725350
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | HG02886.hp1 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.383+326T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725350 | ||||||
| chr2:48725355
|
C | A | 1 | a0002c0002t0002g0038 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.383+321G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725355 | ||||||
| chr2:48725435
|
C | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.383+241G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725435 | ||||||
| chr2:48725485
|
G | A | 359 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(356): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.383+191C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725485 | ||||||
| chr2:48725499
|
C | A | 1 | a0001c0001t0001g0141 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.383+177G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725499 | ||||||
| chr2:48725510
|
G | A | 47 | a0001c0001t0001g0039a0001c0001t0001g0117a0001c0001t0001g0154others(44): Show | 47 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.383+166C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725510 | ||||||
| chr2:48725562
|
C | G | 359 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(356): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.383+114G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 4/10 | chr2 | 48725562 | ||||||
| chr2:48725805
|
A | G | 3 | a0002c0002t0001g0234a0002c0002t0004g0232a0002c0002t0004g0294 | 3 | HG02622.hp2 HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.309-55T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48725805 | ||||||
| chr2:48725886
|
G | A | 1 | a0002c0005t0002g0144 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.309-136C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48725886 | ||||||
| chr2:48726070
|
C | T | 353 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(350): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.309-320G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726070 | ||||||
| chr2:48726117
|
C | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0089others(77): Show | 84 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.309-367G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726117 | ||||||
| chr2:48726210
|
C | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(184): Show | 193 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.309-460G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726210 | ||||||
| chr2:48726390
|
G | C | 1 | a0001c0001t0001g0290 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.309-640C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726390 | ||||||
| chr2:48726421
|
G | A | 2 | a0002c0002t0005g0250a0002c0002t0005g0326 | 2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.309-671C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726421 | ||||||
| chr2:48726495
|
G | A | 1 | a0002c0002t0001g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.309-745C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726495 | ||||||
| chr2:48726601
|
G | C | 47 | a0001c0001t0001g0006a0001c0001t0001g0085a0001c0001t0001g0102others(44): Show | 49 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.309-851C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726601 | ||||||
| chr2:48726626
|
C | T | 2 | a0002c0002t0001g0297a0006c0007t0003g0296 | 2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.309-876G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726626 | ||||||
| chr2:48726730
|
G | A | 1 | a0001c0001t0001g0256 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.309-980C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726730 | ||||||
| chr2:48726808
|
G | A | 29 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0102others(26): Show | 30 | HG00280.hp1 HG00558.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.309-1058C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726808 | ||||||
| chr2:48726840
|
T | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0017others(109): Show | 114 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.309-1090A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48726840 | ||||||
| chr2:48727031
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.309-1281A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727031 | ||||||
| chr2:48727142
|
T | A | 1 | a0001c0001t0001g0180 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.309-1392A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727142 | ||||||
| chr2:48727230
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.309-1480C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727230 | ||||||
| chr2:48727288
|
A | C | 2 | a0001c0001t0001g0264a0002c0002t0001g0246 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.309-1538T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727288 | ||||||
| chr2:48727289
|
A | T | 2 | a0001c0001t0001g0264a0002c0002t0001g0246 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.309-1539T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727289 | ||||||
| chr2:48727461
|
A | G | 1 | a0003c0003t0002g0340 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.308+1692T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727461 | ||||||
| chr2:48727644
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.308+1509A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727644 | ||||||
| chr2:48727703
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.308+1450T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727703 | ||||||
| chr2:48727766
|
T | C | 106 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0026others(103): Show | 107 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.308+1387A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727766 | ||||||
| chr2:48727890
|
T | C | 1 | a0002c0002t0003g0262 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.308+1263A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727890 | ||||||
| chr2:48727901
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.308+1252T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727901 | ||||||
| chr2:48727942
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.308+1211T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48727942 | ||||||
| chr2:48728046
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.308+1107G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728046 | ||||||
| chr2:48728083
|
A | G | 2 | a0002c0002t0001g0070a0002c0002t0001g0079 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.308+1070T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728083 | ||||||
| chr2:48728087
|
GT | G | 105 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0094others(102): Show | 106 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.308+1065delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728087 | ||||||
| chr2:48728087
|
GTT | G | 104 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(101): Show | 111 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.308+1064_308+1065d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728087 | ||||||
| chr2:48728087
|
GTTT | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.308+1063_308+1065d others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728087 | ||||||
| chr2:48728175
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.308+978A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728175 | ||||||
| chr2:48728198
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.308+955G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728198 | ||||||
| chr2:48728231
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.308+922G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728231 | ||||||
| chr2:48728266
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.308+887G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728266 | ||||||
| chr2:48728348
|
T | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.308+805A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728348 | ||||||
| chr2:48728362
|
A | G | 1 | a0007c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.308+791T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728362 | ||||||
| chr2:48728422
|
C | G | 1 | a0001c0001t0001g0277 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.308+731G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728422 | ||||||
| chr2:48728510
|
C | G | 1 | a0001c0001t0006g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.308+643G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728510 | ||||||
| chr2:48728531
|
T | C | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.308+622A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728531 | ||||||
| chr2:48728544
|
A | G | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.308+609T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728544 | ||||||
| chr2:48728590
|
T | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(2): Show | 5 | HG00438.hp1 HG02027.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.308+563A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 3/10 | chr2 | 48728590 | ||||||
| chr2:48729278
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.234-51G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729278 | ||||||
| chr2:48729292
|
T | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.234-65A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729292 | ||||||
| chr2:48729332
|
G | C | 1 | a0006c0007t0003g0316 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.234-105C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729332 | ||||||
| chr2:48729336
|
C | T | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.234-109G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729336 | ||||||
| chr2:48729373
|
A | C | 1 | a0001c0001t0001g0158 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.234-146T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729373 | ||||||
| chr2:48729373
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.234-146T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729373 | ||||||
| chr2:48729659
|
A | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02040.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.234-432T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729659 | ||||||
| chr2:48729773
|
T | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02015.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.234-546A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729773 | ||||||
| chr2:48729844
|
T | C | 1 | a0002c0002t0002g0083 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.234-617A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729844 | ||||||
| chr2:48729972
|
AC | A | 2 | a0005c0008t0004g0012a0005c0008t0004g0361 | 3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.234-746delG | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48729972 | ||||||
| chr2:48730016
|
A | G | 1 | a0007c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234-789T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48730016 | ||||||
| chr2:48730206
|
G | A | 1 | a0007c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.234-979C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48730206 | ||||||
| chr2:48730442
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 67 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.233+785T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48730442 | ||||||
| chr2:48730720
|
C | T | 1 | a0004c0004t0001g0336 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.233+507G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48730720 | ||||||
| chr2:48731132
|
C | T | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.233+95G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48731132 | ||||||
| chr2:48731152
|
T | A | 9 | a0002c0002t0001g0016a0002c0002t0001g0030a0002c0002t0001g0037others(6): Show | 10 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+75A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 2/10 | chr2 | 48731152 | ||||||
| chr2:48731456
|
A | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(31): Show | 35 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.162-158T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731456 | ||||||
| chr2:48731487
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 112 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.162-189T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731487 | ||||||
| chr2:48731508
|
C | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 112 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.162-210G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731508 | ||||||
| chr2:48731548
|
G | T | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 112 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.162-250C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731548 | ||||||
| chr2:48731608
|
C | T | 2 | a0003c0003t0002g0340a0003c0003t0002g0355 | 2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.162-310G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731608 | ||||||
| chr2:48731889
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02040.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.162-591G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48731889 | ||||||
| chr2:48732135
|
G | T | 1 | a0001c0001t0001g0241 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.162-837C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732135 | ||||||
| chr2:48732166
|
G | T | 1 | a0001c0001t0001g0303 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.162-868C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732166 | ||||||
| chr2:48732280
|
G | A | 1 | a0006c0007t0003g0296 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.162-982C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732280 | ||||||
| chr2:48732312
|
G | A | 32 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(29): Show | 33 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-1014C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732312 | ||||||
| chr2:48732398
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(105): Show | 115 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.162-1100A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732398 | ||||||
| chr2:48732405
|
C | T | 2 | a0005c0008t0004g0012a0005c0008t0004g0361 | 3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.162-1107G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732405 | ||||||
| chr2:48732464
|
A | G | 244 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(241): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.162-1166T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732464 | ||||||
| chr2:48732582
|
C | G | 1 | a0001c0001t0001g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.162-1284G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732582 | ||||||
| chr2:48732628
|
C | T | 3 | a0002c0002t0004g0068a0003c0003t0004g0334a0003c0003t0004g0338 | 3 | HG02559.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.162-1330G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732628 | ||||||
| chr2:48732734
|
C | T | 1 | a0002c0002t0001g0209 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.162-1436G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732734 | ||||||
| chr2:48732766
|
G | A | 1 | a0001c0001t0001g0319 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.162-1468C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732766 | ||||||
| chr2:48732824
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.162-1526T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732824 | ||||||
| chr2:48732864
|
A | G | 1 | a0002c0005t0001g0206 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.162-1566T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732864 | ||||||
| chr2:48732893
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(49): Show | 55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.162-1595C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732893 | ||||||
| chr2:48732973
|
A | G | 8 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0299others(5): Show | 8 | HG00423.hp1 HG02523.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-1675T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48732973 | ||||||
| chr2:48733173
|
T | G | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-1875A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733173 | ||||||
| chr2:48733178
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(147): Show | 157 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.162-1880T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733178 | ||||||
| chr2:48733194
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162-1896G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733194 | ||||||
| chr2:48733372
|
G | A | 1 | a0001c0001t0006g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.162-2074C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733372 | ||||||
| chr2:48733380
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.162-2082A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733380 | ||||||
| chr2:48733501
|
C | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(49): Show | 55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.162-2203G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733501 | ||||||
| chr2:48733671
|
G | A | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(49): Show | 55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.162-2373C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733671 | ||||||
| chr2:48733765
|
T | G | 1 | a0001c0001t0001g0272 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.162-2467A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733765 | ||||||
| chr2:48733804
|
G | A | 6 | a0001c0001t0001g0233a0002c0002t0001g0234a0002c0002t0001g0297others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-2506C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733804 | ||||||
| chr2:48733804
|
G | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-2506C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733804 | ||||||
| chr2:48733936
|
A | G | 1 | a0003c0003t0002g0340 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.162-2638T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48733936 | ||||||
| chr2:48734017
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.162-2719A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734017 | ||||||
| chr2:48734108
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.162-2810C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734108 | ||||||
| chr2:48734147
|
C | A | 2 | a0005c0008t0004g0012a0005c0008t0004g0361 | 3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.162-2849G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734147 | ||||||
| chr2:48734199
|
A | T | 33 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(30): Show | 34 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.162-2901T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734199 | ||||||
| chr2:48734256
|
C | T | 3 | a0002c0002t0004g0068a0003c0003t0004g0334a0003c0003t0004g0338 | 3 | HG02559.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.162-2958G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734256 | ||||||
| chr2:48734257
|
G | T | 52 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(49): Show | 55 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.162-2959C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734257 | ||||||
| chr2:48734312
|
A | G | 1 | a0002c0002t0001g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162-3014T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734312 | ||||||
| chr2:48734418
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.162-3120C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734418 | ||||||
| chr2:48734502
|
A | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(102): Show | 112 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.162-3204T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734502 | ||||||
| chr2:48734523
|
A | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(50): Show | 56 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.162-3225T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734523 | ||||||
| chr2:48734563
|
TTCC | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.162-3268_162-3266d others(5): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734563 | ||||||
| chr2:48734811
|
G | T | 3 | a0002c0002t0001g0016a0002c0002t0001g0030a0002c0002t0001g0037 | 3 | HG02055.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.162-3513C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734811 | ||||||
| chr2:48734858
|
A | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(51): Show | 57 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.162-3560T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734858 | ||||||
| chr2:48734884
|
T | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0040a0001c0001t0001g0061 | 3 | HG02273.hp1 NA19003.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.162-3586A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734884 | ||||||
| chr2:48734888
|
G | A | 2 | a0002c0002t0003g0170a0002c0002t0005g0081 | 2 | HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.162-3590C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734888 | ||||||
| chr2:48734978
|
A | G | 1 | a0002c0002t0003g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162-3680T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48734978 | ||||||
| chr2:48735152
|
G | T | 38 | a0001c0001t0001g0233a0001c0001t0001g0287a0002c0002t0001g0234others(35): Show | 38 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.162-3854C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735152 | ||||||
| chr2:48735216
|
T | A | 4 | a0002c0002t0001g0016a0002c0002t0001g0030a0002c0002t0001g0037others(1): Show | 4 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-3918A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735216 | ||||||
| chr2:48735271
|
T | C | 1 | a0005c0008t0004g0361 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.162-3973A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735271 | ||||||
| chr2:48735296
|
A | T | 1 | a0004c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.162-3998T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735296 | ||||||
| chr2:48735304
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.162-4006C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735304 | ||||||
| chr2:48735411
|
A | G | 3 | a0002c0002t0004g0068a0003c0003t0004g0334a0003c0003t0004g0338 | 3 | HG02559.hp2 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.162-4113T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735411 | ||||||
| chr2:48735485
|
T | C | 12 | a0003c0003t0002g0354a0003c0003t0003g0329a0003c0003t0003g0331others(9): Show | 12 | HG00639.hp2 HG01175.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.162-4187A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735485 | ||||||
| chr2:48735633
|
C | T | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.162-4335G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735633 | ||||||
| chr2:48735674
|
G | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(50): Show | 56 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.162-4376C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735674 | ||||||
| chr2:48735743
|
G | A | 5 | a0001c0001t0001g0136a0002c0002t0002g0009a0002c0002t0002g0084others(2): Show | 6 | HG00642.hp1 HG00738.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-4445C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735743 | ||||||
| chr2:48735763
|
G | A | 2 | a0001c0001t0001g0264a0002c0002t0001g0246 | 2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.162-4465C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735763 | ||||||
| chr2:48735786
|
G | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0134a0001c0001t0001g0135others(5): Show | 9 | NA18944.hp1 NA18952.hp1 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-4488C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735786 | ||||||
| chr2:48735815
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.162-4517A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735815 | ||||||
| chr2:48735921
|
C | T | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0173others(6): Show | 9 | HG00438.hp2 HG02523.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-4623G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48735921 | ||||||
| chr2:48736146
|
A | G | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-4848T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736146 | ||||||
| chr2:48736405
|
C | T | 1 | a0002c0002t0001g0037 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.162-5107G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736405 | ||||||
| chr2:48736490
|
C | T | 2 | a0002c0002t0001g0297a0006c0007t0003g0296 | 2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.162-5192G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736490 | ||||||
| chr2:48736730
|
A | G | 1 | a0004c0004t0001g0359 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.162-5432T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736730 | ||||||
| chr2:48736854
|
T | G | 1 | a0001c0001t0001g0257 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.162-5556A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736854 | ||||||
| chr2:48736891
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.162-5593A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48736891 | ||||||
| chr2:48737045
|
G | A | 47 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0075others(44): Show | 49 | HG00280.hp2 HG00733.hp2 HG01168.hp1 others(46): Show |
intron_variant | MODIFIER | c.162-5747C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737045 | ||||||
| chr2:48737068
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-5770C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737068 | ||||||
| chr2:48737242
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-5944T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737242 | ||||||
| chr2:48737281
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 279 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.162-5983A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737281 | ||||||
| chr2:48737318
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.162-6020C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737318 | ||||||
| chr2:48737427
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162-6129T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737427 | ||||||
| chr2:48737438
|
T | C | 1 | a0001c0001t0001g0303 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.162-6140A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737438 | ||||||
| chr2:48737571
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(190): Show | 204 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.162-6273A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737571 | ||||||
| chr2:48737588
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0002c0002t0002g0109 | 3 | HG02572.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.162-6290G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737588 | ||||||
| chr2:48737589
|
G | A | 3 | a0002c0002t0001g0244a0002c0002t0003g0014a0002c0002t0003g0245 | 3 | HG02486.hp1 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162-6291C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737589 | ||||||
| chr2:48737613
|
G | A | 2 | a0001c0001t0001g0292a0002c0002t0003g0293 | 2 | HG00738.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.162-6315C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737613 | ||||||
| chr2:48737753
|
C | A | 1 | a0001c0001t0006g0224 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.162-6455G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737753 | ||||||
| chr2:48737846
|
A | T | 1 | a0004c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.162-6548T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737846 | ||||||
| chr2:48737860
|
C | G | 1 | a0001c0001t0001g0230 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.162-6562G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737860 | ||||||
| chr2:48737883
|
A | C | 33 | a0001c0001t0001g0287a0002c0002t0004g0068a0002c0002t0008g0098others(30): Show | 33 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.162-6585T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48737883 | ||||||
| chr2:48738093
|
A | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0172a0001c0001t0001g0218others(1): Show | 4 | HG00140.hp1 HG01515.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-6795T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738093 | ||||||
| chr2:48738189
|
C | A | 1 | a0002c0002t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.162-6891G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738189 | ||||||
| chr2:48738464
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 128 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.162-7166A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738464 | ||||||
| chr2:48738569
|
C | T | 1 | a0003c0003t0003g0348 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.162-7271G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738569 | ||||||
| chr2:48738643
|
G | A | 1 | a0002c0002t0002g0169 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.162-7345C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738643 | ||||||
| chr2:48738707
|
T | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 128 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.162-7409A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738707 | ||||||
| chr2:48738739
|
A | G | 30 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0122others(27): Show | 31 | HG00408.hp1 HG00544.hp2 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.162-7441T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738739 | ||||||
| chr2:48738842
|
T | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(191): Show | 205 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.162-7544A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738842 | ||||||
| chr2:48738846
|
T | C | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.162-7548A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738846 | ||||||
| chr2:48738900
|
A | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 127 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.162-7602T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738900 | ||||||
| chr2:48738916
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(176): Show | 190 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.162-7618G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738916 | ||||||
| chr2:48738999
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.162-7701A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48738999 | ||||||
| chr2:48739007
|
T | C | 74 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(71): Show | 76 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.162-7709A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739007 | ||||||
| chr2:48739021
|
C | G | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(56): Show | 62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.162-7723G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739021 | ||||||
| chr2:48739200
|
T | C | 2 | a0001c0001t0001g0057a0001c0001t0001g0327 | 2 | HG01361.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.162-7902A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739200 | ||||||
| chr2:48739215
|
G | C | 2 | a0001c0001t0001g0125a0001c0001t0006g0126 | 2 | NA19060.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.162-7917C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739215 | ||||||
| chr2:48739255
|
G | A | 6 | a0003c0003t0001g0330a0003c0003t0001g0353a0003c0003t0001g0357others(3): Show | 6 | HG01257.hp1 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-7957C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739255 | ||||||
| chr2:48739288
|
T | C | 1 | a0002c0002t0003g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162-7990A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739288 | ||||||
| chr2:48739316
|
A | G | 1 | a0002c0002t0002g0308 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.162-8018T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739316 | ||||||
| chr2:48739375
|
C | T | 2 | a0001c0001t0001g0075a0007c0009t0004g0069 | 2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.162-8077G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739375 | ||||||
| chr2:48739379
|
A | G | 10 | a0001c0001t0001g0287a0003c0003t0002g0346a0003c0003t0002g0347others(7): Show | 10 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-8081T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739379 | ||||||
| chr2:48739501
|
TG | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(7): Show | 12 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.162-8204delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739501 | ||||||
| chr2:48739518
|
T | C | 3 | a0001c0001t0001g0129a0002c0002t0001g0244a0002c0002t0003g0245 | 3 | HG02451.hp2 HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.162-8220A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739518 | ||||||
| chr2:48739604
|
T | C | 4 | a0002c0002t0005g0250a0002c0002t0005g0326a0005c0008t0004g0012others(1): Show | 5 | HG02630.hp1 HG02896.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-8306A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739604 | ||||||
| chr2:48739637
|
G | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.162-8339C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739637 | ||||||
| chr2:48739668
|
G | C | 9 | a0001c0001t0001g0287a0003c0003t0002g0346a0003c0003t0002g0347others(6): Show | 9 | HG00733.hp1 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.162-8370C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739668 | ||||||
| chr2:48739746
|
G | C | 2 | a0002c0002t0003g0110a0002c0002t0003g0112 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.162-8448C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739746 | ||||||
| chr2:48739814
|
A | T | 10 | a0001c0001t0001g0207a0001c0001t0001g0265a0001c0001t0001g0266others(7): Show | 10 | HG01109.hp1 HG01358.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-8516T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739814 | ||||||
| chr2:48739863
|
C | G | 1 | a0002c0002t0002g0038 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.162-8565G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739863 | ||||||
| chr2:48739882
|
G | A | 1 | a0002c0002t0001g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.162-8584C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739882 | ||||||
| chr2:48739992
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.162-8694G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739992 | ||||||
| chr2:48739993
|
G | A | 5 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0301others(2): Show | 5 | NA18945.hp2 NA18950.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-8695C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48739993 | ||||||
| chr2:48740004
|
C | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-8706G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740004 | ||||||
| chr2:48740035
|
C | T | 1 | a0002c0002t0002g0200 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.162-8737G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740035 | ||||||
| chr2:48740128
|
T | C | 1 | a0001c0001t0001g0258 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.162-8830A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740128 | ||||||
| chr2:48740181
|
G | A | 2 | a0002c0002t0001g0244a0002c0002t0003g0245 | 2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.162-8883C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740181 | ||||||
| chr2:48740246
|
G | T | 2 | a0004c0004t0001g0332a0004c0004t0001g0351 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.162-8948C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740246 | ||||||
| chr2:48740334
|
C | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(56): Show | 62 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.162-9036G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740334 | ||||||
| chr2:48740416
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 127 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.162-9118A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740416 | ||||||
| chr2:48740441
|
T | G | 2 | a0003c0003t0003g0343a0004c0004t0001g0344 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.162-9143A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740441 | ||||||
| chr2:48740462
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0006t0001g0225others(1): Show | 4 | HG00741.hp2 HG01361.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-9164C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740462 | ||||||
| chr2:48740543
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 203 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.162-9245A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740543 | ||||||
| chr2:48740544
|
G | A | 4 | a0001c0001t0001g0111a0002c0002t0003g0110a0002c0002t0003g0112others(1): Show | 4 | HG01243.hp1 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-9246C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740544 | ||||||
| chr2:48740557
|
G | A | 4 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0301others(1): Show | 4 | NA18950.hp2 NA18974.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-9259C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740557 | ||||||
| chr2:48740566
|
C | G | 15 | a0001c0001t0001g0071a0001c0001t0001g0075a0002c0002t0001g0070others(12): Show | 16 | HG01891.hp2 HG02145.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.162-9268G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740566 | ||||||
| chr2:48740596
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 127 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.162-9298A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740596 | ||||||
| chr2:48740600
|
C | A | 2 | a0001c0001t0001g0207a0002c0002t0003g0262 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162-9302G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740600 | ||||||
| chr2:48740606
|
C | T | 2 | a0001c0001t0001g0207a0002c0002t0003g0262 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.162-9308G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740606 | ||||||
| chr2:48740619
|
G | A | 1 | a0002c0002t0002g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.162-9321C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740619 | ||||||
| chr2:48740770
|
A | T | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9472T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740770 | ||||||
| chr2:48740782
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9484A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740782 | ||||||
| chr2:48740783
|
G | A | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9485C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740783 | ||||||
| chr2:48740789
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9491G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740789 | ||||||
| chr2:48740811
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.162-9513A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740811 | ||||||
| chr2:48740845
|
G | T | 2 | a0003c0003t0002g0340a0003c0003t0002g0355 | 2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.162-9547C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740845 | ||||||
| chr2:48740899
|
C | G | 1 | a0004c0004t0001g0337 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.162-9601G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48740899 | ||||||
| chr2:48741067
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.162-9769C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741067 | ||||||
| chr2:48741085
|
G | A | 1 | a0002c0002t0003g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162-9787C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741085 | ||||||
| chr2:48741121
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.162-9823A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741121 | ||||||
| chr2:48741235
|
G | A | 5 | a0002c0002t0001g0209a0002c0002t0004g0189a0002c0002t0004g0210others(2): Show | 5 | HG01884.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-9937C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741235 | ||||||
| chr2:48741362
|
G | A | 1 | a0001c0006t0001g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.162-10064C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741362 | ||||||
| chr2:48741427
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-10129T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741427 | ||||||
| chr2:48741453
|
T | TA | 73 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(70): Show | 75 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.162-10156dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741453 | ||||||
| chr2:48741464
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-10166C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741464 | ||||||
| chr2:48741538
|
C | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(245): Show | 259 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.162-10240G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741538 | ||||||
| chr2:48741592
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-10294T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741592 | ||||||
| chr2:48741662
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162-10364C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741662 | ||||||
| chr2:48741691
|
G | A | 26 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0299others(23): Show | 26 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.162-10393C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741691 | ||||||
| chr2:48741787
|
G | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-10489C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741787 | ||||||
| chr2:48741949
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.162-10651C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741949 | ||||||
| chr2:48741953
|
C | T | 2 | a0005c0008t0004g0012a0005c0008t0004g0361 | 3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.162-10655G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48741953 | ||||||
| chr2:48742026
|
G | A | 57 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0001g0090others(54): Show | 57 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.162-10728C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742026 | ||||||
| chr2:48742050
|
T | G | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.162-10752A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742050 | ||||||
| chr2:48742093
|
A | G | 37 | a0001c0001t0001g0287a0002c0002t0003g0097a0002c0002t0004g0068others(34): Show | 37 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.162-10795T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742093 | ||||||
| chr2:48742118
|
G | A | 1 | a0002c0002t0001g0270 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.162-10820C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742118 | ||||||
| chr2:48742184
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.162-10886A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742184 | ||||||
| chr2:48742330
|
C | T | 1 | a0007c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162-11032G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742330 | ||||||
| chr2:48742452
|
C | T | 2 | a0001c0001t0001g0319a0002c0002t0001g0325 | 2 | HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.162-11154G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742452 | ||||||
| chr2:48742497
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.162-11199T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742497 | ||||||
| chr2:48742550
|
G | A | 1 | a0007c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162-11252C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742550 | ||||||
| chr2:48742605
|
C | T | 1 | a0002c0002t0005g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162-11307G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742605 | ||||||
| chr2:48742606
|
A | G | 1 | a0002c0002t0005g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.162-11308T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742606 | ||||||
| chr2:48742622
|
T | G | 4 | a0001c0001t0001g0287a0003c0003t0002g0346a0003c0003t0002g0347others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.162-11324A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742622 | ||||||
| chr2:48742645
|
G | A | 1 | a0002c0002t0002g0281 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.162-11347C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742645 | ||||||
| chr2:48742681
|
G | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0040 | 2 | HG02273.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.162-11383C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742681 | ||||||
| chr2:48742711
|
T | A | 1 | a0002c0002t0001g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162-11413A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742711 | ||||||
| chr2:48742769
|
C | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(52): Show | 58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.162-11471G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742769 | ||||||
| chr2:48742923
|
C | T | 55 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(52): Show | 58 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.162-11625G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742923 | ||||||
| chr2:48742971
|
G | T | 3 | a0002c0002t0003g0014a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02630.hp1 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.162-11673C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48742971 | ||||||
| chr2:48743006
|
G | A | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.162-11708C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743006 | ||||||
| chr2:48743020
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.162-11722C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743020 | ||||||
| chr2:48743070
|
T | A | 1 | a0007c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.162-11772A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743070 | ||||||
| chr2:48743100
|
G | T | 1 | a0001c0001t0001g0298 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.162-11802C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743100 | ||||||
| chr2:48743145
|
A | G | 2 | a0002c0002t0001g0244a0002c0002t0003g0245 | 2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.162-11847T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743145 | ||||||
| chr2:48743180
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.162-11882G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743180 | ||||||
| chr2:48743203
|
A | G | 1 | a0004c0004t0001g0359 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.162-11905T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743203 | ||||||
| chr2:48743247
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.162-11949G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743247 | ||||||
| chr2:48743296
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.162-11998G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743296 | ||||||
| chr2:48743319
|
G | C | 1 | a0002c0002t0005g0213 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.162-12021C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743319 | ||||||
| chr2:48743326
|
C | A | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-12028G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743326 | ||||||
| chr2:48743346
|
G | A | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162-12048C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743346 | ||||||
| chr2:48743430
|
T | A | 1 | a0002c0002t0002g0038 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.161+12081A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743430 | ||||||
| chr2:48743431
|
A | G | 1 | a0002c0002t0002g0038 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.161+12080T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743431 | ||||||
| chr2:48743451
|
G | A | 59 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(56): Show | 62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.161+12060C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743451 | ||||||
| chr2:48743645
|
C | A | 3 | a0001c0001t0001g0156a0002c0002t0002g0155a0002c0002t0002g0157 | 3 | NA18948.hp1 NA18951.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.161+11866G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743645 | ||||||
| chr2:48743650
|
A | T | 1 | a0002c0002t0008g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.161+11861T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743650 | ||||||
| chr2:48743748
|
G | A | 4 | a0001c0001t0001g0314a0002c0002t0001g0315a0002c0002t0002g0313others(1): Show | 4 | HG00280.hp1 HG02486.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+11763C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743748 | ||||||
| chr2:48743891
|
A | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02015.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.161+11620T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743891 | ||||||
| chr2:48743957
|
G | C | 1 | a0001c0001t0001g0259 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.161+11554C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48743957 | ||||||
| chr2:48744003
|
A | G | 1 | a0002c0002t0001g0092 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.161+11508T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744003 | ||||||
| chr2:48744015
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(216): Show | 231 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.161+11496G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744015 | ||||||
| chr2:48744107
|
G | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.161+11404C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744107 | ||||||
| chr2:48744114
|
A | G | 3 | a0002c0002t0001g0295a0002c0002t0001g0297a0006c0007t0003g0296 | 3 | HG02451.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.161+11397T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744114 | ||||||
| chr2:48744183
|
G | T | 20 | a0001c0001t0001g0207a0001c0001t0001g0263a0001c0001t0001g0264others(17): Show | 20 | HG01109.hp1 HG01358.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.161+11328C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744183 | ||||||
| chr2:48744229
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.161+11282A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744229 | ||||||
| chr2:48744266
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.161+11245A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744266 | ||||||
| chr2:48744304
|
A | G | 1 | a0002c0002t0008g0098 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.161+11207T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744304 | ||||||
| chr2:48744343
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.161+11168T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744343 | ||||||
| chr2:48744376
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.161+11135A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744376 | ||||||
| chr2:48744417
|
A | G | 6 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.161+11094T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744417 | ||||||
| chr2:48744431
|
C | G | 2 | a0002c0002t0004g0080a0002c0002t0005g0067 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.161+11080G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744431 | ||||||
| chr2:48744505
|
C | T | 3 | a0002c0002t0001g0016a0002c0002t0001g0030a0002c0002t0001g0037 | 3 | HG02055.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.161+11006G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744505 | ||||||
| chr2:48744540
|
G | A | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+10971C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744540 | ||||||
| chr2:48744576
|
C | G | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(357): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.161+10935G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744576 | ||||||
| chr2:48744577
|
A | G | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(357): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.161+10934T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744577 | ||||||
| chr2:48744586
|
A | C | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(357): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.161+10925T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744586 | ||||||
| chr2:48744643
|
T | C | 1 | a0002c0002t0001g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161+10868A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744643 | ||||||
| chr2:48744755
|
C | T | 2 | a0002c0002t0001g0244a0002c0002t0003g0245 | 2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.161+10756G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744755 | ||||||
| chr2:48744835
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(60): Show | 66 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.161+10676T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744835 | ||||||
| chr2:48744853
|
A | G | 3 | a0001c0001t0001g0111a0002c0002t0003g0110a0002c0002t0003g0112 | 3 | HG01243.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.161+10658T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744853 | ||||||
| chr2:48744899
|
G | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.161+10612C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744899 | ||||||
| chr2:48744932
|
T | C | 3 | a0002c0002t0001g0295a0002c0002t0001g0297a0006c0007t0003g0296 | 3 | HG02451.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.161+10579A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744932 | ||||||
| chr2:48744935
|
C | G | 1 | a0001c0001t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.161+10576G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744935 | ||||||
| chr2:48744968
|
C | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 6 | NA18952.hp1 NA19010.hp1 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+10543G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48744968 | ||||||
| chr2:48745032
|
G | A | 2 | a0004c0004t0001g0332a0004c0004t0001g0351 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.161+10479C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745032 | ||||||
| chr2:48745070
|
A | G | 2 | a0001c0001t0001g0036a0001c0006t0001g0260 | 2 | HG00099.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.161+10441T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745070 | ||||||
| chr2:48745166
|
G | T | 6 | a0001c0001t0001g0094a0001c0001t0001g0251a0001c0001t0001g0252others(3): Show | 6 | NA18968.hp2 NA18983.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+10345C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745166 | ||||||
| chr2:48745401
|
G | A | 1 | a0007c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161+10110C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745401 | ||||||
| chr2:48745413
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(150): Show | 161 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(158): Show |
intron_variant | MODIFIER | c.161+10098T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745413 | ||||||
| chr2:48745458
|
A | C | 1 | a0001c0001t0001g0193 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.161+10053T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745458 | ||||||
| chr2:48745525
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 231 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.161+9986T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745525 | ||||||
| chr2:48745535
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(114): Show | 125 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(122): Show |
intron_variant | MODIFIER | c.161+9976G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745535 | ||||||
| chr2:48745880
|
GA | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(7): Show | 12 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.161+9630delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745880 | ||||||
| chr2:48745881
|
A | G | 31 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0299others(28): Show | 31 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.161+9630T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745881 | ||||||
| chr2:48745882
|
A | G | 8 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(5): Show | 10 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.161+9629T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745882 | ||||||
| chr2:48745914
|
T | C | 1 | a0004c0004t0001g0356 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.161+9597A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745914 | ||||||
| chr2:48745949
|
C | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.161+9562G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745949 | ||||||
| chr2:48745988
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 126 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.161+9523C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745988 | ||||||
| chr2:48745991
|
C | G | 3 | a0002c0002t0003g0014a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02630.hp1 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161+9520G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48745991 | ||||||
| chr2:48746023
|
T | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.161+9488A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746023 | ||||||
| chr2:48746056
|
A | G | 28 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0299others(25): Show | 28 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.161+9455T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746056 | ||||||
| chr2:48746213
|
G | A | 3 | a0002c0002t0001g0247a0002c0002t0001g0248a0002c0002t0001g0283 | 3 | HG02723.hp1 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.161+9298C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746213 | ||||||
| chr2:48746221
|
G | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.161+9290C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746221 | ||||||
| chr2:48746252
|
G | C | 2 | a0002c0002t0001g0229a0002c0002t0002g0150 | 2 | HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.161+9259C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746252 | ||||||
| chr2:48746278
|
A | G | 1 | a0007c0009t0004g0099 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161+9233T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746278 | ||||||
| chr2:48746296
|
A | C | 4 | a0001c0001t0001g0233a0002c0002t0001g0234a0002c0002t0004g0232others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+9215T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746296 | ||||||
| chr2:48746889
|
T | G | 2 | a0002c0002t0001g0139a0002c0002t0001g0204 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.161+8622A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746889 | ||||||
| chr2:48746990
|
CCT | C | 27 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0299others(24): Show | 27 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.161+8519_161+8520d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48746990 | ||||||
| chr2:48747091
|
C | CT | 21 | a0001c0001t0001g0006a0001c0001t0001g0062a0001c0001t0001g0089others(18): Show | 23 | HG01099.hp1 HG01106.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.161+8419dupA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747091 | ||||||
| chr2:48747091
|
C | CTT | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(85): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.161+8418_161+8419d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747091 | ||||||
| chr2:48747131
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 271 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.161+8380T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747131 | ||||||
| chr2:48747264
|
T | C | 2 | a0003c0003t0003g0343a0004c0004t0001g0344 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.161+8247A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747264 | ||||||
| chr2:48747358
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(240): Show | 254 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.161+8153G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747358 | ||||||
| chr2:48747495
|
G | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.161+8016C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747495 | ||||||
| chr2:48747510
|
T | A | 28 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0299others(25): Show | 28 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.161+8001A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747510 | ||||||
| chr2:48747600
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.161+7911G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747600 | ||||||
| chr2:48747611
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0029others(1): Show | 4 | HG02027.hp2 HG02132.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+7900A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747611 | ||||||
| chr2:48747728
|
T | G | 1 | a0001c0006t0001g0260 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.161+7783A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747728 | ||||||
| chr2:48747758
|
C | G | 9 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG00423.hp1 HG02523.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.161+7753G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747758 | ||||||
| chr2:48747830
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.161+7681G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747830 | ||||||
| chr2:48747843
|
C | T | 2 | a0002c0002t0001g0244a0002c0002t0003g0245 | 2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.161+7668G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48747843 | ||||||
| chr2:48748159
|
C | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.161+7352G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748159 | ||||||
| chr2:48748353
|
G | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 127 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.161+7158C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748353 | ||||||
| chr2:48748407
|
C | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.161+7104G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748407 | ||||||
| chr2:48748492
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.161+7019C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748492 | ||||||
| chr2:48748667
|
T | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0002c0002t0002g0109 | 3 | HG02572.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.161+6844A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748667 | ||||||
| chr2:48748689
|
T | C | 2 | a0002c0002t0003g0110a0002c0002t0003g0112 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6822A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748689 | ||||||
| chr2:48748693
|
T | G | 2 | a0002c0002t0003g0110a0002c0002t0003g0112 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6818A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748693 | ||||||
| chr2:48748694
|
A | T | 2 | a0002c0002t0003g0110a0002c0002t0003g0112 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6817T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748694 | ||||||
| chr2:48748695
|
C | G | 2 | a0002c0002t0003g0110a0002c0002t0003g0112 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6816G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748695 | ||||||
| chr2:48748700
|
A | G | 2 | a0002c0002t0003g0110a0002c0002t0003g0112 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6811T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748700 | ||||||
| chr2:48748701
|
T | A | 2 | a0002c0002t0003g0110a0002c0002t0003g0112 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6810A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748701 | ||||||
| chr2:48748703
|
C | G | 2 | a0002c0002t0003g0110a0002c0002t0003g0112 | 2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.161+6808G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748703 | ||||||
| chr2:48748856
|
C | T | 2 | a0002c0002t0001g0244a0002c0002t0003g0245 | 2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.161+6655G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748856 | ||||||
| chr2:48748970
|
C | T | 3 | a0001c0001t0001g0156a0002c0002t0002g0155a0002c0002t0002g0157 | 3 | NA18948.hp1 NA18951.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.161+6541G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48748970 | ||||||
| chr2:48749071
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(258): Show | 274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.161+6440C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749071 | ||||||
| chr2:48749088
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.161+6423T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749088 | ||||||
| chr2:48749088
|
A | T | 1 | a0001c0001t0001g0305 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.161+6423T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749088 | ||||||
| chr2:48749093
|
A | C | 2 | a0003c0003t0003g0343a0004c0004t0001g0344 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.161+6418T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749093 | ||||||
| chr2:48749167
|
C | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0027a0001c0001t0001g0035 | 4 | HG00621.hp2 HG01109.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+6344G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749167 | ||||||
| chr2:48749200
|
A | G | 2 | a0005c0008t0004g0012a0005c0008t0004g0361 | 3 | HG03139.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.161+6311T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749200 | ||||||
| chr2:48749209
|
C | T | 2 | a0002c0002t0005g0250a0002c0002t0005g0326 | 2 | HG02630.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.161+6302G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749209 | ||||||
| chr2:48749259
|
G | A | 1 | a0004c0004t0001g0336 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.161+6252C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749259 | ||||||
| chr2:48749276
|
G | A | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+6235C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749276 | ||||||
| chr2:48749314
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.161+6197A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749314 | ||||||
| chr2:48749438
|
C | G | 16 | a0003c0003t0001g0330a0003c0003t0001g0353a0003c0003t0001g0357others(13): Show | 16 | HG00639.hp2 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.161+6073G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749438 | ||||||
| chr2:48749493
|
A | G | 3 | a0002c0002t0003g0014a0002c0002t0005g0250a0002c0002t0005g0326 | 3 | HG02630.hp1 HG02896.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161+6018T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749493 | ||||||
| chr2:48749496
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.161+6015C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749496 | ||||||
| chr2:48749641
|
G | A | 1 | a0003c0003t0003g0348 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.161+5870C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749641 | ||||||
| chr2:48749658
|
T | C | 1 | a0001c0001t0001g0303 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.161+5853A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749658 | ||||||
| chr2:48749720
|
T | TA | 31 | a0001c0001t0001g0304a0002c0002t0004g0068a0002c0002t0008g0098others(28): Show | 31 | HG00733.hp1 HG01071.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.161+5790dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749720 | ||||||
| chr2:48749720
|
TA | T | 72 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(69): Show | 75 | HG00280.hp2 HG00558.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.161+5790delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749720 | ||||||
| chr2:48749736
|
A | G | 8 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0142others(5): Show | 8 | HG02027.hp2 HG02165.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+5775T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749736 | ||||||
| chr2:48749742
|
G | GA | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187 | 3 | NA19056.hp2 NA19088.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.161+5768dupT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749742 | ||||||
| chr2:48749747
|
A | C | 46 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(43): Show | 48 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.161+5764T>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749747 | ||||||
| chr2:48749831
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.161+5680G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749831 | ||||||
| chr2:48749876
|
T | G | 1 | a0003c0003t0001g0358 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.161+5635A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749876 | ||||||
| chr2:48749968
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.161+5543C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749968 | ||||||
| chr2:48749981
|
T | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0101a0001c0001t0001g0102others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.161+5530A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48749981 | ||||||
| chr2:48750045
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG00408.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.161+5466T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750045 | ||||||
| chr2:48750268
|
T | C | 1 | a0001c0001t0001g0298 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.161+5243A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750268 | ||||||
| chr2:48750488
|
A | G | 1 | a0003c0003t0003g0360 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.161+5023T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750488 | ||||||
| chr2:48750639
|
C | T | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(252): Show | 268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.161+4872G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750639 | ||||||
| chr2:48750682
|
A | T | 33 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0089others(30): Show | 36 | HG00558.hp2 HG00609.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.161+4829T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750682 | ||||||
| chr2:48750810
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.161+4701G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750810 | ||||||
| chr2:48750823
|
G | A | 1 | a0004c0004t0001g0359 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.161+4688C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750823 | ||||||
| chr2:48750970
|
C | T | 6 | a0003c0003t0001g0330a0003c0003t0001g0357a0003c0003t0002g0340others(3): Show | 6 | HG01168.hp2 HG01169.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+4541G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48750970 | ||||||
| chr2:48751020
|
A | G | 94 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(91): Show | 100 | HG00280.hp2 HG00558.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.161+4491T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751020 | ||||||
| chr2:48751125
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(152): Show | 166 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.161+4386G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751125 | ||||||
| chr2:48751143
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.161+4368C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751143 | ||||||
| chr2:48751178
|
A | G | 1 | a0002c0002t0002g0268 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.161+4333T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751178 | ||||||
| chr2:48751253
|
AT | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 175 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.161+4257delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751253 | ||||||
| chr2:48751258
|
T | G | 1 | a0002c0002t0005g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.161+4253A>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751258 | ||||||
| chr2:48751311
|
C | A | 1 | a0001c0001t0001g0230 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.161+4200G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751311 | ||||||
| chr2:48751335
|
C | G | 12 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265others(9): Show | 12 | HG01109.hp1 HG01358.hp1 HG02300.hp2 others(9): Show |
intron_variant | MODIFIER | c.161+4176G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751335 | ||||||
| chr2:48751626
|
T | C | 29 | a0001c0001t0001g0289a0001c0001t0001g0298a0001c0001t0001g0299others(26): Show | 29 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.161+3885A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751626 | ||||||
| chr2:48751973
|
C | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0026 | 2 | NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.161+3538G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48751973 | ||||||
| chr2:48752141
|
G | T | 1 | a0006c0007t0003g0316 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.161+3370C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752141 | ||||||
| chr2:48752356
|
T | A | 4 | a0002c0002t0001g0261a0002c0002t0001g0284a0002c0002t0005g0250others(1): Show | 4 | HG01109.hp1 HG02559.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+3155A>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752356 | ||||||
| chr2:48752466
|
T | C | 4 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(1): Show | 4 | NA18940.hp1 NA18982.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+3045A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752466 | ||||||
| chr2:48752493
|
C | G | 5 | a0002c0002t0001g0295a0002c0002t0001g0297a0002c0002t0003g0097others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+3018G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752493 | ||||||
| chr2:48752527
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.161+2984A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752527 | ||||||
| chr2:48752529
|
CT | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(248): Show | 264 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(261): Show |
intron_variant | MODIFIER | c.161+2981delA | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752529 | ||||||
| chr2:48752798
|
G | C | 1 | a0001c0001t0001g0027 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.161+2713C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752798 | ||||||
| chr2:48752864
|
T | C | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+2647A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752864 | ||||||
| chr2:48752981
|
C | CG | 44 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0091others(41): Show | 46 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.161+2529dupC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752981 | ||||||
| chr2:48752981
|
C | CGGGG | 20 | a0001c0001t0001g0007a0001c0001t0001g0129a0001c0001t0001g0130others(17): Show | 21 | HG00642.hp1 HG00738.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.161+2526_161+2529d others(6): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752981 | ||||||
| chr2:48752981
|
C | CGGGGGGG others(5): Show |
1 | a0002c0002t0003g0128 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.161+2518_161+2529d others(14): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752981 | ||||||
| chr2:48752981
|
CG | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0062others(29): Show | 34 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.161+2529delC | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752981 | ||||||
| chr2:48752985
|
G | C | 1 | a0004c0004t0001g0349 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.161+2526C>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752985 | ||||||
| chr2:48752986
|
G | GA | 15 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG00408.hp2 HG00544.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+2524_161+2525i others(3): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752986 | ||||||
| chr2:48752986
|
G | GGGGCGGG others(12): Show |
2 | a0003c0003t0001g0330a0003c0003t0001g0357 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.161+2524_161+2525i others(21): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752986 | ||||||
| chr2:48752986
|
G | GGGGTGGG others(13): Show |
1 | a0004c0004t0001g0350 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.161+2524_161+2525i others(22): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752986 | ||||||
| chr2:48752986
|
G | T | 2 | a0004c0004t0001g0332a0004c0004t0001g0351 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.161+2525C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752986 | ||||||
| chr2:48752987
|
G | A | 48 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(45): Show | 52 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.161+2524C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752987 | ||||||
| chr2:48752988
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0062 | 3 | HG00621.hp2 HG02040.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.161+2523C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752988 | ||||||
| chr2:48752988
|
G | T | 1 | a0002c0002t0002g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161+2523C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752988 | ||||||
| chr2:48752991
|
G | GGGGGGGG others(15): Show |
2 | a0001c0001t0001g0299a0004c0004t0001g0333 | 2 | HG02523.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(24): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGGGGG others(14): Show |
3 | a0003c0003t0003g0360a0003c0003t0004g0334a0004c0004t0001g0335 | 3 | HG01261.hp1 HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(23): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGGGGT others(14): Show |
6 | a0001c0001t0001g0289a0001c0001t0001g0318a0001c0001t0001g0319others(3): Show | 6 | HG01169.hp1 HG02056.hp2 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(23): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGGGGT others(13): Show |
9 | a0001c0001t0001g0106a0001c0001t0001g0300a0003c0003t0004g0338others(6): Show | 10 | HG00423.hp1 HG00639.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(22): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGGGTG others(14): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0105 | 4 | HG01099.hp1 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(23): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGGGTG others(13): Show |
8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0321others(5): Show | 8 | HG00735.hp1 HG01256.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(22): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGGGTG others(12): Show |
11 | a0001c0001t0001g0301a0001c0001t0001g0303a0001c0001t0001g0304others(8): Show | 11 | HG01243.hp2 HG01952.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(21): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGGGTG others(9): Show |
3 | a0002c0002t0001g0295a0002c0002t0004g0294a0006c0007t0003g0296 | 3 | HG03209.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(18): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGGTGG others(12): Show |
3 | a0001c0001t0001g0298a0003c0003t0002g0355a0004c0004t0001g0356 | 3 | HG01257.hp1 HG01496.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(21): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGGTGG others(11): Show |
14 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0309others(11): Show | 14 | HG00280.hp1 HG01081.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(20): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGTGGG others(11): Show |
1 | a0002c0002t0002g0324 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.161+2519_161+2520i others(20): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGTGGG others(10): Show |
5 | a0002c0002t0002g0317a0003c0003t0002g0346a0004c0004t0001g0328others(2): Show | 5 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(19): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGGTGGG others(7): Show |
1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+2519_161+2520i others(16): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGTGGGG others(9): Show |
2 | a0003c0003t0002g0347a0003c0003t0003g0348 | 2 | HG01069.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.161+2519_161+2520i others(18): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GGGTGGGG others(6): Show |
1 | a0002c0002t0001g0297 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161+2519_161+2520i others(15): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | GT | 5 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0125others(2): Show | 5 | HG02132.hp1 HG03834.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+2519_161+2520i others(3): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752991
|
G | T | 3 | a0003c0003t0001g0330a0003c0003t0001g0357a0004c0004t0001g0350 | 3 | HG01515.hp2 HG01517.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.161+2520C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752991 | ||||||
| chr2:48752994
|
G | T | 3 | a0002c0002t0001g0244a0002c0002t0003g0245a0002c0002t0004g0068 | 3 | HG02486.hp1 HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.161+2517C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48752994 | ||||||
| chr2:48753017
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.161+2494G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753017 | ||||||
| chr2:48753236
|
A | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(347): Show | 363 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.161+2275T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753236 | ||||||
| chr2:48753368
|
G | T | 68 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(65): Show | 70 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.161+2143C>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753368 | ||||||
| chr2:48753625
|
A | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(5): Show | 9 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.161+1886T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753625 | ||||||
| chr2:48753627
|
A | T | 2 | a0002c0002t0001g0244a0002c0002t0003g0245 | 2 | HG02486.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.161+1884T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753627 | ||||||
| chr2:48753682
|
G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0102a0001c0001t0001g0103others(3): Show | 7 | HG01099.hp1 HG01123.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.161+1829C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753682 | ||||||
| chr2:48753799
|
A | G | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | HG02040.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.161+1712T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753799 | ||||||
| chr2:48753805
|
A | AGT | 16 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0063others(13): Show | 18 | HG00280.hp2 HG00741.hp2 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+1704_161+1705d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753805 | ||||||
| chr2:48753805
|
A | AGTGTGT | 72 | a0001c0001t0001g0006a0001c0001t0001g0101a0001c0001t0001g0102others(69): Show | 74 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.161+1700_161+1705d others(8): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753805 | ||||||
| chr2:48753805
|
AGT | A | 69 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0071others(66): Show | 72 | HG00733.hp2 HG01081.hp2 HG01109.hp1 others(69): Show |
intron_variant | MODIFIER | c.161+1704_161+1705d others(4): Show |
LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753805 | ||||||
| chr2:48753913
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | NA18941.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.161+1598G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48753913 | ||||||
| chr2:48754109
|
A | G | 5 | a0002c0002t0001g0295a0002c0002t0001g0297a0002c0002t0003g0097others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+1402T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754109 | ||||||
| chr2:48754173
|
A | T | 3 | a0001c0001t0001g0111a0002c0002t0003g0110a0002c0002t0003g0112 | 3 | HG01243.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.161+1338T>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754173 | ||||||
| chr2:48754225
|
A | G | 1 | a0003c0003t0003g0331 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.161+1286T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754225 | ||||||
| chr2:48754251
|
A | G | 1 | a0002c0002t0003g0097 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.161+1260T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754251 | ||||||
| chr2:48754339
|
G | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0063a0002c0002t0003g0064others(1): Show | 6 | HG01433.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+1172C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754339 | ||||||
| chr2:48754415
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0108a0002c0002t0002g0109 | 3 | HG02572.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.161+1096G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754415 | ||||||
| chr2:48754507
|
A | G | 76 | a0001c0001t0001g0006a0001c0001t0001g0101a0001c0001t0001g0102others(73): Show | 78 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.161+1004T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754507 | ||||||
| chr2:48754595
|
A | AC | 22 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0085others(19): Show | 22 | HG01106.hp1 HG01261.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.161+915dupG | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754595 | ||||||
| chr2:48754598
|
C | A | 28 | a0001c0001t0001g0289a0001c0001t0001g0299a0001c0001t0001g0300others(25): Show | 28 | HG00280.hp1 HG00423.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.161+913G>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754598 | ||||||
| chr2:48754638
|
A | G | 1 | a0004c0004t0001g0328 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.161+873T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754638 | ||||||
| chr2:48754653
|
C | T | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+858G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754653 | ||||||
| chr2:48754758
|
A | G | 16 | a0001c0001t0001g0071a0001c0001t0001g0075a0002c0002t0001g0070others(13): Show | 17 | HG01891.hp2 HG02145.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.161+753T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754758 | ||||||
| chr2:48754822
|
A | G | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+689T>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754822 | ||||||
| chr2:48754835
|
C | T | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+676G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754835 | ||||||
| chr2:48754902
|
G | A | 2 | a0001c0001t0001g0290a0001c0001t0001g0291 | 2 | HG02129.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.161+609C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754902 | ||||||
| chr2:48754925
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(59): Show | 67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.161+586C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754925 | ||||||
| chr2:48754958
|
CA | C | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(59): Show | 67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.161+552delT | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754958 | ||||||
| chr2:48754974
|
C | T | 1 | a0002c0002t0003g0014 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161+537G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754974 | ||||||
| chr2:48754993
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(59): Show | 67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.161+518C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48754993 | ||||||
| chr2:48755011
|
G | A | 3 | a0002c0002t0005g0326a0005c0008t0004g0012a0005c0008t0004g0361 | 4 | HG02896.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+500C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755011 | ||||||
| chr2:48755035
|
C | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(59): Show | 67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.161+476G>A | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755035 | ||||||
| chr2:48755123
|
G | A | 2 | a0001c0001t0001g0292a0002c0002t0003g0293 | 2 | HG00738.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.161+388C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755123 | ||||||
| chr2:48755219
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(54): Show | 62 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.161+292C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755219 | ||||||
| chr2:48755346
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(88): Show | 96 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.161+165A>G | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755346 | ||||||
| chr2:48755483
|
C | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(55): Show | 63 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.161+28G>C | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755483 | ||||||
| chr2:48755494
|
G | A | 1 | a0001c0001t0001g0327 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.161+17C>T | LHCGR | ENSG00000138039.15 | transcript | ENST00000294954.12 | protein_coding | 1/10 | chr2 | 48755494 |