| geneid | 254251 |
|---|---|
| ensemblid | ENSG00000178177.17 |
| hgncid | 30776 |
| symbol | LCORL |
| name | ligand dependent nuclear receptor corepressor like |
| refseq_nuc | NM_001394446.1 |
| refseq_prot | NP_001381375.1 |
| ensembl_nuc | ENST00000635767.2 |
| ensembl_prot | ENSP00000490600.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 17841187 |
| end | 18021755 |
| strand | - |
| ver | v1.2 |
| region | chr4:17841187-18021755 |
| region5000 | chr4:17836187-18026755 |
| regionname0 | LCORL_chr4_17841187_18021755 |
| regionname5000 | LCORL_chr4_17836187_18026755 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1871 | 142 | 36 | 25 | 60 | 1 | 18 | 48 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002 | 0/0 | 1870 | 78 | 17 | 17 | 37 | 1 | 6 | 30 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0003 | 0/0 | 1871 | 18 | 0 | 0 | 12 | 0 | 6 | 12 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004 | 0/0 | 1871 | 14 | 14 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0005 | 0/0 | 1871 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0006 | 0/0 | 1871 | 5 | 3 | 1 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0007 | 0/0 | 1871 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0008 | 0/0 | 1871 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0009 | 0/0 | 1871 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0010 | 0/0 | 1871 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0011 | 0/0 | 1871 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0012 | 0/0 | 1871 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0013 | 0/0 | 1870 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0014 | 0/0 | 1871 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0015 | 0/0 | 1871 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0016 | 0/0 | 1871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0017 | 0/0 | 1871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0018 | 0/0 | 1871 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0019 | 0/0 | 1871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0020 | 0/0 | 1870 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0021 | 0/0 | 1871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0022 | 0/0 | 1871 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0023 | 0/0 | 1871 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 5616 | 104 | 30 | 14 | 44 | 1 | 13 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0002 | 0/0 | 5613 | 77 | 16 | 17 | 37 | 1 | 6 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0003 | 0/0 | 5616 | 37 | 6 | 10 | 16 | 0 | 5 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0004 | 0/0 | 5616 | 18 | 0 | 0 | 12 | 0 | 6 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0005 | 0/0 | 5616 | 12 | 12 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0006 | 0/0 | 5616 | 6 | 6 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0007 | 0/0 | 5616 | 5 | 3 | 1 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0008 | 0/0 | 5616 | 3 | 1 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0009 | 0/0 | 5616 | 3 | 0 | 0 | 3 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0010 | 0/0 | 5616 | 3 | 0 | 2 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0011 | 0/0 | 5616 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0012 | 0/0 | 5616 | 2 | 0 | 0 | 0 | 2 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0013 | 0/0 | 5613 | 2 | 0 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0014 | 0/0 | 5616 | 2 | 0 | 0 | 0 | 0 | 2 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0015 | 0/0 | 5616 | 2 | 0 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0016 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0017 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0018 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0019 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0020 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0021 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0022 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0023 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0024 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0025 | 0/0 | 5616 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0026 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0027 | 0/0 | 5616 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0028 | 0/0 | 5616 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| c0029 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 4705 | 72 | 8 | 17 | 33 | 1 | 12 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0002 | 0/0 | 4706 | 62 | 1 | 16 | 37 | 0 | 8 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0003 | 0/0 | 4705 | 38 | 5 | 11 | 15 | 2 | 5 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0004 | 0/0 | 4705 | 20 | 4 | 0 | 10 | 0 | 6 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0005 | 0/0 | 4709 | 11 | 10 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0006 | 0/0 | 4706 | 9 | 7 | 1 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0007 | 1/0 | 4706 | 9 | 8 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0008 | 0/0 | 4706 | 8 | 8 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0009 | 0/0 | 4706 | 6 | 0 | 0 | 6 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0010 | 0/0 | 4705 | 6 | 4 | 0 | 2 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0011 | 0/0 | 4710 | 5 | 5 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0012 | 0/0 | 4706 | 5 | 0 | 0 | 5 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0013 | 0/0 | 4705 | 4 | 2 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0014 | 0/0 | 4709 | 3 | 3 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0015 | 0/0 | 4705 | 2 | 0 | 0 | 0 | 0 | 2 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0016 | 0/0 | 4705 | 2 | 0 | 0 | 2 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0017 | 0/0 | 4705 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0018 | 0/0 | 4705 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0019 | 0/0 | 4705 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0020 | 0/0 | 4706 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0021 | 0/0 | 4706 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0022 | 0/0 | 4705 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0023 | 0/0 | 4710 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0024 | 0/0 | 4706 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0025 | 0/0 | 4705 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0026 | 0/0 | 4705 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0027 | 0/0 | 4705 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0028 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0029 | 0/0 | 4705 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0030 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0031 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0032 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0033 | 0/0 | 4706 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0034 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0035 | 0/0 | 4706 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0036 | 0/0 | 4706 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0037 | 0/0 | 4706 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0038 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0039 | 0/0 | 4706 | 1 | 0 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0040 | 0/0 | 4706 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| t0041 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5616 | 104 | 30 | 14 | 44 | 1 | 13 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0003 | 0/0 | 5616 | 37 | 6 | 10 | 16 | 0 | 5 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0025 | 0/0 | 5616 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002 | 0/0 | 5613 | 77 | 16 | 17 | 37 | 1 | 6 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0026 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0003c0004 | 0/0 | 5616 | 18 | 0 | 0 | 12 | 0 | 6 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0005 | 0/0 | 5616 | 12 | 12 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0020 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0024 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0005c0006 | 0/0 | 5616 | 6 | 6 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0006c0007 | 0/0 | 5616 | 5 | 3 | 1 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0007c0008 | 0/0 | 5616 | 3 | 1 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0008c0010 | 0/0 | 5616 | 3 | 0 | 2 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0009c0009 | 0/0 | 5616 | 3 | 0 | 0 | 3 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0010c0014 | 0/0 | 5616 | 2 | 0 | 0 | 0 | 0 | 2 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0011c0027 | 0/0 | 5616 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0011c0028 | 0/0 | 5616 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0012c0012 | 0/0 | 5616 | 2 | 0 | 0 | 0 | 2 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0013c0013 | 0/0 | 5613 | 2 | 0 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0014c0011 | 0/0 | 5616 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0015c0015 | 0/0 | 5616 | 2 | 0 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0016c0029 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0017c0017 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0018c0021 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0019c0019 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0020c0023 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0021c0018 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0022c0022 | 0/0 | 5616 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0023c0016 | 0/0 | 5616 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 10320 | 62 | 7 | 13 | 30 | 1 | 10 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0002 | 0/0 | 10321 | 5 | 0 | 0 | 4 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0005 | 0/0 | 10324 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0006 | 0/0 | 10321 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0007 | 1/0 | 10321 | 9 | 8 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0009 | 0/0 | 10321 | 6 | 0 | 0 | 6 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0010 | 0/0 | 10320 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0012 | 0/0 | 10321 | 2 | 0 | 0 | 2 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0016 | 0/0 | 10320 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0017 | 0/0 | 10320 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0018 | 0/0 | 10320 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0019 | 0/0 | 10320 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0021 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0023 | 0/0 | 10325 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0024 | 0/0 | 10321 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0027 | 0/0 | 10320 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0029 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0036 | 0/0 | 10321 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0040 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0001t0041 | 0/0 | 10320 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0003t0001 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0003t0003 | 0/0 | 10320 | 34 | 5 | 9 | 15 | 0 | 5 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0003t0022 | 0/0 | 10320 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0003t0025 | 0/0 | 10320 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0001c0025t0026 | 0/0 | 10320 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0001 | 0/0 | 10317 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0002 | 0/0 | 10318 | 53 | 1 | 14 | 32 | 0 | 6 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0005 | 0/0 | 10321 | 8 | 7 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0012 | 0/0 | 10318 | 3 | 0 | 0 | 3 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0014 | 0/0 | 10321 | 3 | 3 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0020 | 0/0 | 10318 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0021 | 0/0 | 10318 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0033 | 0/0 | 10318 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0034 | 0/0 | 10318 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0035 | 0/0 | 10318 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0037 | 0/0 | 10318 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0038 | 0/0 | 10318 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0002t0039 | 0/0 | 10318 | 1 | 0 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0002c0026t0005 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0003c0004t0002 | 0/0 | 10321 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0003c0004t0004 | 0/0 | 10320 | 15 | 0 | 0 | 9 | 0 | 6 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0003c0004t0010 | 0/0 | 10320 | 2 | 0 | 0 | 2 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0005t0004 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0005t0008 | 0/0 | 10321 | 8 | 8 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0005t0010 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0005t0030 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0005t0031 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0020t0032 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0004c0024t0013 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0005c0006t0005 | 0/0 | 10324 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0005c0006t0011 | 0/0 | 10325 | 5 | 5 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0006c0007t0006 | 0/0 | 10321 | 5 | 3 | 1 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0007c0008t0013 | 0/0 | 10320 | 3 | 1 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0008c0010t0001 | 0/0 | 10320 | 3 | 0 | 2 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0009c0009t0001 | 0/0 | 10320 | 3 | 0 | 0 | 3 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0010c0014t0015 | 0/0 | 10320 | 2 | 0 | 0 | 0 | 0 | 2 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0011c0027t0001 | 0/0 | 10320 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0011c0028t0001 | 0/0 | 10320 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0012c0012t0003 | 0/0 | 10320 | 2 | 0 | 0 | 0 | 2 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0013c0013t0002 | 0/0 | 10318 | 2 | 0 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0014c0011t0004 | 0/0 | 10320 | 2 | 2 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0015c0015t0003 | 0/0 | 10320 | 2 | 0 | 2 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0016c0029t0006 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0017c0017t0006 | 0/0 | 10321 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0018c0021t0004 | 0/0 | 10320 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0019c0019t0010 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0020c0023t0002 | 0/0 | 10318 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0021c0018t0028 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0022c0022t0016 | 0/0 | 10320 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| a0023c0016t0004 | 0/0 | 10320 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | copy fasta | chr4 | 17836187 | 18026755 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0188 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0005g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0007g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0009g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0009g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0009g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0010g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0010g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0012g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0016g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0017g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0017g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0018g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0018g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0019g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0019g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0021g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0023g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0024g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0027g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0029g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0036g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0040g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0001t0041g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0022g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0003t0025g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0001c0025t0026g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0012g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0012g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0014g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0020g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0020g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0021g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0033g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0034g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0035g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0037g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0038g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0002t0039g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0002c0026t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0010g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0003c0004t0010g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0008g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0008g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0010g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0030g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0005t0031g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0020t0032g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0004c0024t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0005c0006t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0005c0006t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0005c0006t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0005c0006t0011g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0005c0006t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0005c0006t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0006c0007t0006g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0006c0007t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0006c0007t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0006c0007t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0006c0007t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0007c0008t0013g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0007c0008t0013g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0007c0008t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0008c0010t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0008c0010t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0008c0010t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0009c0009t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0009c0009t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0009c0009t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0010c0014t0015g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0010c0014t0015g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0011c0027t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0011c0028t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0012c0012t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0013c0013t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0013c0013t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0014c0011t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0014c0011t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0015c0015t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0015c0015t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0016c0029t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0017c0017t0006g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0018c0021t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0019c0019t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0020c0023t0002g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0021c0018t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0022c0022t0016g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| a0023c0016t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00423 | hp1 | a0001 | c0003 | t0003 | g0257 | EAS | CHS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00423 | hp2 | a0001 | c0001 | t0009 | g0139 | EAS | CHS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00438 | hp1 | a0001 | c0001 | t0009 | g0173 | EAS | CHS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00438 | hp2 | a0002 | c0002 | t0012 | g0051 | EAS | CHS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00639 | hp1 | a0001 | c0003 | t0003 | g0251 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00673 | hp1 | a0018 | c0021 | t0004 | g0095 | EAS | CHS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | CHS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00735 | hp1 | a0015 | c0015 | t0003 | g0235 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00735 | hp2 | a0013 | c0013 | t0002 | g0074 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00738 | hp1 | a0013 | c0013 | t0002 | g0073 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0234 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01069 | hp1 | a0008 | c0010 | t0001 | g0189 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01071 | hp1 | a0008 | c0010 | t0001 | g0190 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01074 | hp1 | a0001 | c0003 | t0025 | g0264 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01081 | hp1 | a0002 | c0002 | t0035 | g0040 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01081 | hp2 | a0002 | c0002 | t0005 | g0116 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01099 | hp2 | a0001 | c0003 | t0003 | g0271 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0060 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01109 | hp2 | a0007 | c0008 | t0013 | g0218 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01169 | hp1 | a0001 | c0003 | t0003 | g0233 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01175 | hp2 | a0001 | c0003 | t0003 | g0270 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01192 | hp1 | a0001 | c0025 | t0026 | g0205 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01192 | hp2 | a0001 | c0003 | t0003 | g0253 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01243 | hp1 | a0007 | c0008 | t0013 | g0217 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0258 | AMR | PUR | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0087 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01258 | hp2 | a0015 | c0015 | t0003 | g0242 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0265 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01358 | hp1 | a0001 | c0001 | t0027 | g0142 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01358 | hp2 | a0006 | c0007 | t0006 | g0272 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01515 | hp2 | a0012 | c0012 | t0003 | g0002 | EUR | IBS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01517 | hp1 | a0012 | c0012 | t0003 | g0002 | EUR | IBS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01517 | hp2 | a0002 | c0002 | t0039 | g0057 | EUR | IBS | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01884 | hp1 | a0007 | c0008 | t0013 | g0219 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01891 | hp1 | a0021 | c0018 | t0028 | g0003 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01891 | hp2 | a0002 | c0002 | t0014 | g0212 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0044 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0048 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01952 | hp1 | a0001 | c0003 | t0003 | g0238 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0067 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02004 | hp1 | a0011 | c0028 | t0001 | g0137 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0043 | AMR | PEL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02027 | hp1 | a0001 | c0003 | t0003 | g0261 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02040 | hp1 | a0001 | c0003 | t0022 | g0243 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0239 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02055 | hp2 | a0004 | c0005 | t0008 | g0281 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0267 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02056 | hp2 | a0009 | c0009 | t0001 | g0178 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02071 | hp1 | a0022 | c0022 | t0016 | g0138 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0244 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02129 | hp1 | a0001 | c0003 | t0003 | g0269 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02132 | hp1 | a0001 | c0003 | t0003 | g0254 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02132 | hp2 | a0001 | c0001 | t0009 | g0164 | EAS | KHV | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02145 | hp1 | a0004 | c0005 | t0030 | g0290 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02145 | hp2 | a0005 | c0006 | t0011 | g0208 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02257 | hp1 | a0002 | c0002 | t0005 | g0117 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02257 | hp2 | a0001 | c0003 | t0003 | g0268 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02451 | hp1 | a0006 | c0007 | t0006 | g0278 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02572 | hp1 | a0005 | c0006 | t0011 | g0223 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02572 | hp2 | a0001 | c0003 | t0003 | g0236 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02602 | hp1 | a0001 | c0003 | t0003 | g0240 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02602 | hp2 | a0003 | c0004 | t0004 | g0097 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02615 | hp1 | a0016 | c0029 | t0006 | g0285 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02615 | hp2 | a0002 | c0002 | t0005 | g0112 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0263 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0228 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02630 | hp2 | a0014 | c0011 | t0004 | g0092 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02683 | hp2 | a0006 | c0007 | t0006 | g0250 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0077 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02717 | hp1 | a0001 | c0001 | t0019 | g0204 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02717 | hp2 | a0002 | c0002 | t0014 | g0211 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02735 | hp1 | a0011 | c0027 | t0001 | g0161 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02809 | hp1 | a0004 | c0005 | t0031 | g0284 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02809 | hp2 | a0002 | c0002 | t0034 | g0015 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02818 | hp1 | a0002 | c0002 | t0005 | g0209 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02818 | hp2 | a0005 | c0006 | t0005 | g0231 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02886 | hp1 | a0004 | c0005 | t0004 | g0220 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02886 | hp2 | a0001 | c0001 | t0018 | g0175 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0121 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0226 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02922 | hp1 | a0004 | c0005 | t0008 | g0280 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02965 | hp1 | a0004 | c0005 | t0008 | g0288 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0133 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02970 | hp1 | a0004 | c0024 | t0013 | g0088 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02970 | hp2 | a0001 | c0001 | t0017 | g0199 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02976 | hp1 | a0002 | c0002 | t0005 | g0210 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02976 | hp2 | a0002 | c0002 | t0020 | g0275 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03017 | hp1 | a0003 | c0004 | t0004 | g0107 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03017 | hp2 | a0020 | c0023 | t0002 | g0005 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03041 | hp1 | a0019 | c0019 | t0010 | g0221 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0120 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03098 | hp2 | a0002 | c0002 | t0021 | g0008 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03139 | hp1 | a0014 | c0011 | t0004 | g0093 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03139 | hp2 | a0017 | c0017 | t0006 | g0273 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03209 | hp1 | a0005 | c0006 | t0011 | g0230 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03209 | hp2 | a0006 | c0007 | t0006 | g0274 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0237 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03225 | hp2 | a0002 | c0002 | t0038 | g0013 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03453 | hp1 | a0004 | c0005 | t0008 | g0289 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03453 | hp2 | a0001 | c0001 | t0021 | g0225 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03486 | hp2 | a0004 | c0020 | t0032 | g0279 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03490 | hp1 | a0003 | c0004 | t0004 | g0105 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03490 | hp2 | a0010 | c0014 | t0015 | g0248 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03491 | hp2 | a0001 | c0003 | t0003 | g0249 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03492 | hp1 | a0003 | c0004 | t0004 | g0104 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0246 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03516 | hp2 | a0006 | c0007 | t0006 | g0277 | AFR | ESN | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03540 | hp2 | a0005 | c0006 | t0011 | g0222 | AFR | GWD | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03579 | hp2 | a0004 | c0005 | t0010 | g0227 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03654 | hp1 | a0003 | c0004 | t0004 | g0106 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03669 | hp2 | a0010 | c0014 | t0015 | g0259 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03704 | hp1 | a0001 | c0001 | t0036 | g0075 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03704 | hp2 | a0001 | c0001 | t0041 | g0152 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03710 | hp1 | a0001 | c0003 | t0003 | g0241 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03710 | hp2 | a0008 | c0010 | t0001 | g0197 | SAS | PJL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0072 | SAS | BEB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03927 | hp1 | a0003 | c0004 | t0004 | g0096 | SAS | BEB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0066 | SAS | BEB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG04115 | hp2 | a0001 | c0003 | t0003 | g0266 | SAS | STU | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0026 | SAS | STU | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18522 | hp1 | a0001 | c0003 | t0003 | g0262 | AFR | YRI | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18522 | hp2 | a0023 | c0016 | t0004 | g0091 | AFR | YRI | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18906 | hp1 | a0002 | c0002 | t0020 | g0276 | AFR | YRI | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18906 | hp2 | a0002 | c0002 | t0005 | g0118 | AFR | YRI | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18941 | hp1 | a0003 | c0004 | t0004 | g0101 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18942 | hp2 | a0002 | c0002 | t0012 | g0058 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18944 | hp2 | a0001 | c0001 | t0024 | g0156 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18946 | hp2 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18948 | hp2 | a0009 | c0009 | t0001 | g0186 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18949 | hp1 | a0003 | c0004 | t0004 | g0110 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18951 | hp1 | a0001 | c0001 | t0016 | g0140 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18959 | hp1 | a0002 | c0002 | t0037 | g0052 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18959 | hp2 | a0003 | c0004 | t0004 | g0099 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18961 | hp2 | a0003 | c0004 | t0002 | g0109 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18968 | hp1 | a0001 | c0003 | t0003 | g0256 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18970 | hp2 | a0003 | c0004 | t0004 | g0103 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18981 | hp2 | a0001 | c0001 | t0012 | g0082 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18985 | hp2 | a0002 | c0002 | t0012 | g0035 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18986 | hp1 | a0003 | c0004 | t0010 | g0102 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18986 | hp2 | a0002 | c0002 | t0033 | g0070 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18990 | hp1 | a0003 | c0004 | t0004 | g0094 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18991 | hp2 | a0003 | c0004 | t0004 | g0119 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18998 | hp1 | a0003 | c0004 | t0010 | g0100 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19002 | hp2 | a0001 | c0003 | t0003 | g0252 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19005 | hp2 | a0001 | c0003 | t0003 | g0245 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19006 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19010 | hp2 | a0001 | c0003 | t0003 | g0215 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19012 | hp1 | a0003 | c0004 | t0004 | g0108 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19030 | hp2 | a0001 | c0001 | t0029 | g0232 | AFR | LWK | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19043 | hp1 | a0004 | c0005 | t0008 | g0282 | AFR | LWK | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19043 | hp2 | a0002 | c0026 | t0005 | g0115 | AFR | LWK | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19054 | hp2 | a0003 | c0004 | t0004 | g0098 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19056 | hp1 | a0001 | c0003 | t0003 | g0216 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19056 | hp2 | a0001 | c0001 | t0009 | g0143 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19068 | hp2 | a0001 | c0003 | t0003 | g0247 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19078 | hp1 | a0003 | c0004 | t0004 | g0127 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19082 | hp1 | a0001 | c0003 | t0003 | g0255 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19082 | hp2 | a0009 | c0009 | t0001 | g0187 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19083 | hp1 | a0001 | c0001 | t0012 | g0062 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19083 | hp2 | a0001 | c0001 | t0009 | g0129 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19085 | hp1 | a0001 | c0001 | t0009 | g0166 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19086 | hp2 | a0001 | c0003 | t0003 | g0260 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19240 | hp1 | a0005 | c0006 | t0011 | g0229 | AFR | YRI | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA19240 | hp2 | a0002 | c0002 | t0005 | g0113 | AFR | YRI | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA20129 | hp1 | a0004 | c0005 | t0008 | g0286 | AFR | ASW | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA20129 | hp2 | a0002 | c0002 | t0014 | g0213 | AFR | ASW | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | GIH | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0076 | AMR | CLM | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0114 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03471 | hp1 | a0001 | c0001 | t0017 | g0198 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG03471 | hp2 | a0004 | c0005 | t0008 | g0283 | AFR | MSL | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG06807 | hp1 | a0002 | c0002 | t0005 | g0111 | AFR | USA | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA20300 | hp1 | a0001 | c0001 | t0018 | g0174 | AFR | USA | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA20300 | hp2 | a0004 | c0005 | t0008 | g0287 | AFR | USA | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA21309 | hp1 | a0001 | c0001 | t0040 | g0224 | AFR | LWK | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| NA21309 | hp2 | a0001 | c0001 | t0023 | g0007 | AFR | LWK | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0188 | REF | REF | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0020 | REF | REF | LCORL_chr4_17836187_18026755 | LCORL | chr4 | 17836187 | 18026755 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17873526
|
G | A | 2 | a0006a0017 | 6 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(3): Show |
missense_variant | MODERATE | c.5464C>T | p.Pro1822Ser | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 5468/10321 | 5464/5616 | 1822/1871 | chr4 | 17873526 | ||
| chr4:17873607
|
T | C | 6 | a0004a0006a0016others(3): Show | 23 | HG01358.hp2 HG01891.hp1 HG02055.hp2 others(20): Show |
missense_variant | MODERATE | c.5383A>G | p.Thr1795Ala | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 5387/10321 | 5383/5616 | 1795/1871 | chr4 | 17873607 | ||
| chr4:17873897
|
G | A | 1 | a0020 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.5093C>T | p.Thr1698Ile | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 5097/10321 | 5093/5616 | 1698/1871 | chr4 | 17873897 | ||
| chr4:17874112
|
TCTC | T | 3 | a0002a0013a0020 | 81 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(78): Show |
disruptive_inframe_deletion | MODERATE | c.4875_4877delGAG | p.Arg1626del | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 4881/10321 | 4875/5616 | 1625/1871 | chr4 | 17874112 | ||
| chr4:17874194
|
A | C | 1 | a0019 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.4796T>G | p.Phe1599Cys | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 4800/10321 | 4796/5616 | 1599/1871 | chr4 | 17874194 | ||
| chr4:17874545
|
G | C | 1 | a0005 | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.4445C>G | p.Thr1482Ser | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 4449/10321 | 4445/5616 | 1482/1871 | chr4 | 17874545 | ||
| chr4:17875320
|
A | G | 1 | a0008 | 3 | HG01069.hp1 HG01071.hp1 HG03710.hp2 |
missense_variant | MODERATE | c.3670T>C | p.Ser1224Pro | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 3674/10321 | 3670/5616 | 1224/1871 | chr4 | 17875320 | ||
| chr4:17875587
|
T | C | 1 | a0023 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.3403A>G | p.Ile1135Val | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 3407/10321 | 3403/5616 | 1135/1871 | chr4 | 17875587 | ||
| chr4:17875662
|
T | G | 1 | a0018 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.3328A>C | p.Thr1110Pro | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 3332/10321 | 3328/5616 | 1110/1871 | chr4 | 17875662 | ||
| chr4:17875677
|
C | G | 1 | a0021 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.3313G>C | p.Asp1105His | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 3317/10321 | 3313/5616 | 1105/1871 | chr4 | 17875677 | ||
| chr4:17875779
|
C | T | 1 | a0022 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.3211G>A | p.Asp1071Asn | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 3215/10321 | 3211/5616 | 1071/1871 | chr4 | 17875779 | ||
| chr4:17876018
|
G | T | 1 | a0012 | 2 | HG01515.hp2 HG01517.hp1 |
missense_variant | MODERATE | c.2972C>A | p.Pro991His | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 2976/10321 | 2972/5616 | 991/1871 | chr4 | 17876018 | ||
| chr4:17876273
|
T | C | 1 | a0013 | 2 | HG00735.hp2 HG00738.hp1 |
missense_variant | MODERATE | c.2717A>G | p.Asn906Ser | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 2721/10321 | 2717/5616 | 906/1871 | chr4 | 17876273 | ||
| chr4:17876371
|
G | T | 1 | a0009 | 3 | HG02056.hp2 NA18948.hp2 NA19082.hp2 |
missense_variant | MODERATE | c.2619C>A | p.Asp873Glu | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 2623/10321 | 2619/5616 | 873/1871 | chr4 | 17876371 | ||
| chr4:17876967
|
A | G | 2 | a0003a0018 | 19 | HG00673.hp1 HG02602.hp2 HG03017.hp1 others(16): Show |
missense_variant | MODERATE | c.2023T>C | p.Ser675Pro | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 2027/10321 | 2023/5616 | 675/1871 | chr4 | 17876967 | ||
| chr4:17877170
|
C | T | 1 | a0023 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.1820G>A | p.Arg607His | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 1824/10321 | 1820/5616 | 607/1871 | chr4 | 17877170 | ||
| chr4:17877347
|
G | T | 1 | a0017 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1643C>A | p.Thr548Lys | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 1647/10321 | 1643/5616 | 548/1871 | chr4 | 17877347 | ||
| chr4:17877444
|
T | G | 1 | a0011 | 2 | HG02004.hp1 HG02735.hp1 |
missense_variant | MODERATE | c.1546A>C | p.Thr516Pro | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 1550/10321 | 1546/5616 | 516/1871 | chr4 | 17877444 | ||
| chr4:17877650
|
T | G | 1 | a0010 | 2 | HG03490.hp2 HG03669.hp2 |
missense_variant | MODERATE | c.1340A>C | p.Glu447Ala | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 1344/10321 | 1340/5616 | 447/1871 | chr4 | 17877650 | ||
| chr4:17877912
|
G | T | 2 | a0014a0023 | 3 | HG02630.hp2 HG03139.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.1078C>A | p.Pro360Thr | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 1082/10321 | 1078/5616 | 360/1871 | chr4 | 17877912 | ||
| chr4:17878149
|
T | C | 1 | a0016 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.841A>G | p.Lys281Glu | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 845/10321 | 841/5616 | 281/1871 | chr4 | 17878149 | ||
| chr4:17909179
|
A | T | 1 | a0007 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
missense_variant | MODERATE | c.597T>A | p.Asn199Lys | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/8 | 601/10321 | 597/5616 | 199/1871 | chr4 | 17909179 | ||
| chr4:17909217
|
T | C | 1 | a0015 | 2 | HG00735.hp1 HG01258.hp2 |
missense_variant | MODERATE | c.559A>G | p.Ile187Val | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/8 | 563/10321 | 559/5616 | 187/1871 | chr4 | 17909217 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17874928
|
G | A | 1 | a0001c0025 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.4062C>T | p.Asn1354Asn | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 4066/10321 | 4062/5616 | 1354/1871 | chr4 | 17874928 | ||
| chr4:17875135
|
A | G | 1 | a0011c0027 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.3855T>C | p.Asn1285Asn | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 3859/10321 | 3855/5616 | 1285/1871 | chr4 | 17875135 | ||
| chr4:17875423
|
G | A | 1 | a0002c0026 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.3567C>T | p.Asp1189Asp | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 3571/10321 | 3567/5616 | 1189/1871 | chr4 | 17875423 | ||
| chr4:17875735
|
A | T | 2 | a0006c0007a0017c0017 | 6 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(3): Show |
synonymous_variant | LOW | c.3255T>A | p.Gly1085Gly | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 3259/10321 | 3255/5616 | 1085/1871 | chr4 | 17875735 | ||
| chr4:17875864
|
A | G | 6 | a0001c0003a0003c0004a0010c0014others(3): Show | 62 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(59): Show |
synonymous_variant | LOW | c.3126T>C | p.Thr1042Thr | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 3130/10321 | 3126/5616 | 1042/1871 | chr4 | 17875864 | ||
| chr4:17876734
|
T | C | 1 | a0004c0020 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.2256A>G | p.Pro752Pro | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 2260/10321 | 2256/5616 | 752/1871 | chr4 | 17876734 | ||
| chr4:17876968
|
A | C | 2 | a0003c0004a0018c0021 | 19 | HG00673.hp1 HG02602.hp2 HG03017.hp1 others(16): Show |
synonymous_variant | LOW | c.2022T>G | p.Pro674Pro | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 2026/10321 | 2022/5616 | 674/1871 | chr4 | 17876968 | ||
| chr4:17877538
|
G | T | 7 | a0004c0005a0004c0020a0006c0007others(4): Show | 22 | HG01358.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
synonymous_variant | LOW | c.1452C>A | p.Ile484Ile | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/8 | 1456/10321 | 1452/5616 | 484/1871 | chr4 | 17877538 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17841197
|
G | T | 1 | a0004c0020t0032 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4691C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 4691 | chr4 | 17841197 | |||||
| chr4:17841225
|
A | T | 1 | a0002c0002t0035 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4663T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 4663 | chr4 | 17841225 | |||||
| chr4:17841277
|
C | T | 2 | a0004c0024t0013a0007c0008t0013 | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4611G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 4611 | chr4 | 17841277 | |||||
| chr4:17841487
|
T | C | 1 | a0004c0005t0031 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4401A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 4401 | chr4 | 17841487 | |||||
| chr4:17841600
|
T | C | 1 | a0001c0001t0017 | 2 | HG02970.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4288A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 4288 | chr4 | 17841600 | |||||
| chr4:17841819
|
T | C | 1 | a0001c0001t0029 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4069A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 4069 | chr4 | 17841819 | |||||
| chr4:17841841
|
A | C | 1 | a0001c0001t0024 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4047T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 4047 | chr4 | 17841841 | |||||
| chr4:17841890
|
A | G | 1 | a0001c0003t0025 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3998T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3998 | chr4 | 17841890 | |||||
| chr4:17841993
|
T | C | 1 | a0001c0001t0036 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3895A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3895 | chr4 | 17841993 | |||||
| chr4:17842325
|
C | T | 1 | a0021c0018t0028 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3563G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3563 | chr4 | 17842325 | |||||
| chr4:17842406
|
G | A | 55 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(52): Show | 201 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*3482C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3482 | chr4 | 17842406 | |||||
| chr4:17842488
|
G | A | 1 | a0001c0025t0026 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3400C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3400 | chr4 | 17842488 | |||||
| chr4:17842611
|
T | A | 1 | a0001c0001t0018 | 2 | HG02886.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3277A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3277 | chr4 | 17842611 | |||||
| chr4:17842627
|
T | C | 7 | a0001c0003t0003a0001c0003t0022a0004c0024t0013others(4): Show | 45 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*3261A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3261 | chr4 | 17842627 | |||||
| chr4:17842661
|
G | A | 1 | a0010c0014t0015 | 2 | HG03490.hp2 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3227C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3227 | chr4 | 17842661 | |||||
| chr4:17842752
|
G | C | 1 | a0004c0020t0032 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3136C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3136 | chr4 | 17842752 | |||||
| chr4:17842757
|
G | A | 3 | a0001c0001t0021a0001c0001t0040a0002c0002t0021 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3131C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3131 | chr4 | 17842757 | |||||
| chr4:17842790
|
C | CTGTT | 7 | a0001c0001t0005a0001c0001t0023a0002c0002t0005others(4): Show | 20 | HG01081.hp2 HG01891.hp2 HG02109.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3094_*3097dupAACA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 3097 | chr4 | 17842790 | |||||
| chr4:17843057
|
C | T | 1 | a0002c0002t0014 | 3 | HG01891.hp2 HG02717.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2831G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2831 | chr4 | 17843057 | |||||
| chr4:17843097
|
A | G | 1 | a0002c0002t0034 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2791T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2791 | chr4 | 17843097 | |||||
| chr4:17843144
|
T | A | 2 | a0004c0024t0013a0007c0008t0013 | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2744A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2744 | chr4 | 17843144 | |||||
| chr4:17843555
|
G | A | 1 | a0001c0001t0027 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2333C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2333 | chr4 | 17843555 | |||||
| chr4:17843615
|
G | C | 55 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(52): Show | 201 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*2273C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2273 | chr4 | 17843615 | |||||
| chr4:17843618
|
C | T | 4 | a0001c0003t0003a0010c0014t0015a0012c0012t0003others(1): Show | 40 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2270G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2270 | chr4 | 17843618 | |||||
| chr4:17843840
|
A | G | 1 | a0004c0005t0030 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2048T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2048 | chr4 | 17843840 | |||||
| chr4:17843847
|
C | T | 5 | a0003c0004t0004a0004c0005t0004a0014c0011t0004others(2): Show | 20 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2041G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2041 | chr4 | 17843847 | |||||
| chr4:17843866
|
T | TA | 2 | a0001c0001t0009a0001c0001t0024 | 7 | HG00423.hp2 HG00438.hp1 HG02132.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2021dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2021 | chr4 | 17843866 | |||||
| chr4:17843869
|
C | G | 4 | a0001c0001t0009a0001c0001t0016a0001c0001t0024others(1): Show | 9 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2019G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 2019 | chr4 | 17843869 | |||||
| chr4:17843979
|
A | C | 1 | a0002c0002t0033 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1909T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1909 | chr4 | 17843979 | |||||
| chr4:17844110
|
A | G | 1 | a0002c0002t0020 | 2 | HG02976.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1778T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1778 | chr4 | 17844110 | |||||
| chr4:17844145
|
G | A | 1 | a0001c0001t0019 | 2 | HG02717.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1743C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1743 | chr4 | 17844145 | |||||
| chr4:17844198
|
C | T | 3 | a0004c0005t0008a0004c0005t0030a0004c0005t0031 | 10 | HG02055.hp2 HG02145.hp1 HG02809.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1690G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1690 | chr4 | 17844198 | |||||
| chr4:17844295
|
T | C | 1 | a0002c0002t0037 | 1 | NA18959.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1593A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1593 | chr4 | 17844295 | |||||
| chr4:17844421
|
T | A | 1 | a0002c0002t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1467A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1467 | chr4 | 17844421 | |||||
| chr4:17844423
|
C | G | 1 | a0002c0002t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1465 | chr4 | 17844423 | |||||
| chr4:17844425
|
T | A | 1 | a0002c0002t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1463A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1463 | chr4 | 17844425 | |||||
| chr4:17844501
|
T | C | 1 | a0002c0002t0039 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1387A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1387 | chr4 | 17844501 | |||||
| chr4:17844662
|
T | TA | 10 | a0001c0001t0006a0001c0001t0023a0004c0005t0008others(7): Show | 26 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1225dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 1225 | chr4 | 17844662 | |||||
| chr4:17844899
|
T | C | 7 | a0001c0003t0003a0001c0003t0022a0004c0024t0013others(4): Show | 45 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*989A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 989 | chr4 | 17844899 | |||||
| chr4:17845459
|
G | A | 1 | a0001c0001t0040 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*429C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 429 | chr4 | 17845459 | |||||
| chr4:17845514
|
A | G | 1 | a0001c0001t0023 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*374T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 374 | chr4 | 17845514 | |||||
| chr4:17845558
|
TA | T | 51 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(48): Show | 204 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*329delT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 329 | chr4 | 17845558 | |||||
| chr4:17845658
|
A | C | 5 | a0001c0003t0003a0001c0003t0022a0010c0014t0015others(2): Show | 41 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*230T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 230 | chr4 | 17845658 | |||||
| chr4:17845700
|
T | C | 2 | a0001c0001t0012a0002c0002t0012 | 5 | HG00438.hp2 NA18942.hp2 NA18981.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*188A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 188 | chr4 | 17845700 | |||||
| chr4:17845714
|
C | A | 1 | a0001c0001t0041 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*174G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 8/8 | 174 | chr4 | 17845714 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:17845937
|
T | C | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5603-36A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17845937 | ||||||
| chr4:17846074
|
T | C | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.5603-173A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846074 | ||||||
| chr4:17846189
|
G | A | 1 | a0001c0001t0029g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5603-288C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846189 | ||||||
| chr4:17846306
|
A | G | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.5603-405T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846306 | ||||||
| chr4:17846403
|
A | T | 1 | a0005c0006t0011g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.5603-502T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846403 | ||||||
| chr4:17846477
|
C | T | 7 | a0001c0003t0003g0233a0001c0003t0003g0234a0001c0003t0003g0241others(4): Show | 7 | HG00735.hp1 HG00738.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.5603-576G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846477 | ||||||
| chr4:17846546
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5603-645G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846546 | ||||||
| chr4:17846614
|
G | A | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5603-713C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846614 | ||||||
| chr4:17846704
|
C | G | 2 | a0004c0005t0008g0280a0004c0005t0008g0281 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5603-803G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846704 | ||||||
| chr4:17846843
|
A | G | 9 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.5603-942T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846843 | ||||||
| chr4:17846936
|
G | C | 44 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(41): Show | 45 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.5603-1035C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846936 | ||||||
| chr4:17846988
|
A | C | 1 | a0001c0001t0029g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5603-1087T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17846988 | ||||||
| chr4:17847113
|
C | T | 1 | a0001c0001t0041g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.5603-1212G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17847113 | ||||||
| chr4:17847133
|
ATTAC | A | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5603-1236_5603-123 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17847133 | ||||||
| chr4:17847136
|
A | G | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5603-1235T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17847136 | ||||||
| chr4:17847141
|
T | G | 23 | a0003c0004t0004g0094a0003c0004t0004g0096a0003c0004t0004g0097others(20): Show | 23 | HG00673.hp1 HG01891.hp1 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.5603-1240A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17847141 | ||||||
| chr4:17847291
|
T | C | 40 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(37): Show | 41 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.5603-1390A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17847291 | ||||||
| chr4:17847937
|
A | G | 2 | a0004c0005t0008g0286a0004c0005t0008g0288 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5603-2036T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17847937 | ||||||
| chr4:17847984
|
T | C | 2 | a0003c0004t0004g0096a0018c0021t0004g0095 | 2 | HG00673.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.5603-2083A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17847984 | ||||||
| chr4:17848001
|
G | C | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5603-2100C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848001 | ||||||
| chr4:17848069
|
G | A | 5 | a0006c0007t0006g0250a0006c0007t0006g0272a0006c0007t0006g0274others(2): Show | 5 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.5603-2168C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848069 | ||||||
| chr4:17848082
|
A | G | 2 | a0001c0001t0021g0225a0001c0001t0040g0224 | 2 | HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.5603-2181T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848082 | ||||||
| chr4:17848108
|
T | C | 1 | a0005c0006t0011g0229 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5603-2207A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848108 | ||||||
| chr4:17848111
|
A | G | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5603-2210T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848111 | ||||||
| chr4:17848231
|
T | TA | 40 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(37): Show | 41 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.5603-2331dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848231 | ||||||
| chr4:17848376
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | NA18943.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.5603-2475C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848376 | ||||||
| chr4:17848663
|
T | C | 40 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(37): Show | 41 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.5603-2762A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848663 | ||||||
| chr4:17848746
|
C | T | 9 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.5603-2845G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848746 | ||||||
| chr4:17848793
|
A | T | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2892T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848793 | ||||||
| chr4:17848797
|
G | A | 20 | a0001c0001t0006g0120a0001c0001t0006g0121a0004c0005t0008g0280others(17): Show | 20 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.5603-2896C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848797 | ||||||
| chr4:17848798
|
G | T | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2897C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848798 | ||||||
| chr4:17848815
|
T | A | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2914A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848815 | ||||||
| chr4:17848834
|
G | T | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2933C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848834 | ||||||
| chr4:17848838
|
T | G | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2937A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848838 | ||||||
| chr4:17848839
|
T | C | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2938A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848839 | ||||||
| chr4:17848852
|
T | G | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2951A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848852 | ||||||
| chr4:17848854
|
A | G | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2953T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848854 | ||||||
| chr4:17848855
|
A | G | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2954T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848855 | ||||||
| chr4:17848856
|
A | C | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2955T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848856 | ||||||
| chr4:17848859
|
C | T | 2 | a0001c0001t0007g0021a0003c0004t0004g0101 | 2 | HG02922.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.5603-2958G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848859 | ||||||
| chr4:17848861
|
G | C | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2960C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848861 | ||||||
| chr4:17848863
|
A | T | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2962T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848863 | ||||||
| chr4:17848871
|
A | T | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2970T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848871 | ||||||
| chr4:17848873
|
A | C | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2972T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848873 | ||||||
| chr4:17848877
|
T | G | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2976A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848877 | ||||||
| chr4:17848881
|
C | G | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2980G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848881 | ||||||
| chr4:17848888
|
T | A | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2987A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848888 | ||||||
| chr4:17848892
|
T | A | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2991A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848892 | ||||||
| chr4:17848894
|
G | C | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2993C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848894 | ||||||
| chr4:17848896
|
A | C | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2995T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848896 | ||||||
| chr4:17848897
|
G | T | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2996C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848897 | ||||||
| chr4:17848898
|
G | C | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5603-2997C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848898 | ||||||
| chr4:17848905
|
C | T | 6 | a0002c0002t0002g0043a0002c0002t0002g0044a0002c0002t0002g0045others(3): Show | 6 | HG01074.hp2 HG01258.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.5603-3004G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848905 | ||||||
| chr4:17848938
|
A | G | 1 | a0001c0001t0010g0226 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5603-3037T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848938 | ||||||
| chr4:17848979
|
G | C | 7 | a0001c0001t0023g0007a0005c0006t0005g0231a0005c0006t0011g0208others(4): Show | 7 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.5603-3078C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17848979 | ||||||
| chr4:17849067
|
C | T | 4 | a0004c0024t0013g0088a0007c0008t0013g0217a0007c0008t0013g0218others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.5603-3166G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17849067 | ||||||
| chr4:17849361
|
G | A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5603-3460C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17849361 | ||||||
| chr4:17849433
|
T | C | 23 | a0003c0004t0004g0094a0003c0004t0004g0096a0003c0004t0004g0097others(20): Show | 23 | HG00673.hp1 HG01891.hp1 HG02602.hp2 others(20): Show |
intron_variant | MODIFIER | c.5603-3532A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17849433 | ||||||
| chr4:17849440
|
C | T | 40 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(37): Show | 41 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.5603-3539G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17849440 | ||||||
| chr4:17849463
|
G | A | 1 | a0002c0026t0005g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5603-3562C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17849463 | ||||||
| chr4:17849504
|
T | A | 1 | a0002c0002t0005g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.5603-3603A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17849504 | ||||||
| chr4:17849527
|
A | C | 44 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(41): Show | 45 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.5603-3626T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17849527 | ||||||
| chr4:17849862
|
GCTAC | G | 5 | a0006c0007t0006g0250a0006c0007t0006g0272a0006c0007t0006g0274others(2): Show | 5 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.5603-3965_5603-396 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17849862 | ||||||
| chr4:17849885
|
G | A | 91 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0009g0129others(88): Show | 92 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.5603-3984C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17849885 | ||||||
| chr4:17850059
|
G | C | 4 | a0004c0024t0013g0088a0007c0008t0013g0217a0007c0008t0013g0218others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.5603-4158C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850059 | ||||||
| chr4:17850197
|
T | C | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5603-4296A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850197 | ||||||
| chr4:17850292
|
A | C | 4 | a0004c0024t0013g0088a0007c0008t0013g0217a0007c0008t0013g0218others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.5603-4391T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850292 | ||||||
| chr4:17850297
|
A | C | 58 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(55): Show | 59 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.5603-4396T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850297 | ||||||
| chr4:17850322
|
A | G | 58 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(55): Show | 59 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.5603-4421T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850322 | ||||||
| chr4:17850343
|
C | T | 9 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.5603-4442G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850343 | ||||||
| chr4:17850398
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5603-4497A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850398 | ||||||
| chr4:17850447
|
C | T | 1 | a0003c0004t0004g0097 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5603-4546G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850447 | ||||||
| chr4:17850497
|
G | C | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.5603-4596C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850497 | ||||||
| chr4:17850548
|
C | T | 2 | a0002c0002t0020g0275a0002c0002t0020g0276 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.5603-4647G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850548 | ||||||
| chr4:17850667
|
G | T | 44 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(41): Show | 45 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.5603-4766C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850667 | ||||||
| chr4:17850704
|
G | A | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5603-4803C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850704 | ||||||
| chr4:17850720
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5603-4819G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850720 | ||||||
| chr4:17850785
|
C | A | 40 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(37): Show | 41 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.5603-4884G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850785 | ||||||
| chr4:17850829
|
G | A | 4 | a0004c0024t0013g0088a0007c0008t0013g0217a0007c0008t0013g0218others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.5603-4928C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850829 | ||||||
| chr4:17850881
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0168 | 2 | HG02698.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.5603-4980T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17850881 | ||||||
| chr4:17851008
|
C | T | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.5603-5107G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851008 | ||||||
| chr4:17851023
|
C | G | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.5603-5122G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851023 | ||||||
| chr4:17851070
|
T | C | 40 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(37): Show | 41 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.5603-5169A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851070 | ||||||
| chr4:17851134
|
G | C | 9 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0023g0007others(6): Show | 9 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.5603-5233C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851134 | ||||||
| chr4:17851134
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5603-5233C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851134 | ||||||
| chr4:17851275
|
T | G | 1 | a0001c0001t0017g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5603-5374A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851275 | ||||||
| chr4:17851301
|
A | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5603-5400T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851301 | ||||||
| chr4:17851323
|
T | C | 2 | a0003c0004t0004g0104a0003c0004t0004g0105 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.5603-5422A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851323 | ||||||
| chr4:17851328
|
C | T | 2 | a0004c0005t0008g0286a0004c0005t0008g0288 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.5603-5427G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851328 | ||||||
| chr4:17851338
|
A | G | 2 | a0001c0003t0001g0239a0001c0003t0025g0264 | 2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.5603-5437T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851338 | ||||||
| chr4:17851626
|
C | A | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5603-5725G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851626 | ||||||
| chr4:17851664
|
G | C | 9 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.5603-5763C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851664 | ||||||
| chr4:17851916
|
A | G | 1 | a0004c0005t0030g0290 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5603-6015T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851916 | ||||||
| chr4:17851953
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5603-6052A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17851953 | ||||||
| chr4:17852042
|
C | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5603-6141G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852042 | ||||||
| chr4:17852103
|
A | C | 44 | a0001c0001t0001g0154a0001c0003t0003g0214a0001c0003t0003g0215others(41): Show | 45 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.5603-6202T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852103 | ||||||
| chr4:17852278
|
CTT | C | 40 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(37): Show | 41 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.5603-6379_5603-637 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852278 | ||||||
| chr4:17852298
|
G | A | 73 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0009g0129others(70): Show | 74 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.5603-6397C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852298 | ||||||
| chr4:17852322
|
A | G | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5603-6421T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852322 | ||||||
| chr4:17852379
|
C | T | 34 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(31): Show | 35 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.5603-6478G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852379 | ||||||
| chr4:17852408
|
T | C | 188 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(185): Show | 190 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.5603-6507A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852408 | ||||||
| chr4:17852422
|
A | G | 1 | a0001c0001t0010g0226 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5603-6521T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852422 | ||||||
| chr4:17852432
|
T | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(201): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.5603-6531A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852432 | ||||||
| chr4:17852490
|
TATACAA | T | 9 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.5603-6595_5603-659 others(10): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852490 | ||||||
| chr4:17852649
|
G | A | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5603-6748C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852649 | ||||||
| chr4:17852650
|
T | A | 1 | a0019c0019t0010g0221 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5603-6749A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852650 | ||||||
| chr4:17852949
|
C | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(78): Show | 82 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.5603-7048G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852949 | ||||||
| chr4:17852953
|
C | G | 1 | a0020c0023t0002g0005 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5603-7052G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852953 | ||||||
| chr4:17852965
|
T | A | 64 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0003g0214others(61): Show | 65 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.5603-7064A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17852965 | ||||||
| chr4:17853045
|
CTTGATTT others(1): Show |
C | 32 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(29): Show | 33 | HG00423.hp1 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.5603-7152_5603-714 others(12): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17853045 | ||||||
| chr4:17853049
|
A | AT | 18 | a0001c0001t0002g0065a0001c0001t0005g0114a0002c0002t0002g0076others(15): Show | 18 | HG00735.hp2 HG00738.hp1 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.5603-7149dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17853049 | ||||||
| chr4:17853049
|
AT | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(135): Show | 139 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.5603-7149delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17853049 | ||||||
| chr4:17853049
|
ATT | A | 20 | a0001c0001t0001g0089a0001c0001t0001g0159a0001c0001t0001g0193others(17): Show | 20 | HG01517.hp2 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.5603-7150_5603-714 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17853049 | ||||||
| chr4:17853049
|
ATTTT | A | 6 | a0001c0003t0003g0236a0001c0003t0003g0237a0001c0003t0003g0258others(3): Show | 6 | HG01243.hp2 HG02040.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.5603-7152_5603-714 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17853049 | ||||||
| chr4:17853145
|
T | C | 40 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(37): Show | 41 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.5603-7244A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17853145 | ||||||
| chr4:17853559
|
T | C | 1 | a0002c0002t0002g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.5603-7658A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17853559 | ||||||
| chr4:17853894
|
TA | T | 73 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0009g0129others(70): Show | 74 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.5603-7994delT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17853894 | ||||||
| chr4:17854092
|
C | T | 1 | a0004c0005t0008g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.5603-8191G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17854092 | ||||||
| chr4:17854093
|
G | C | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5603-8192C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17854093 | ||||||
| chr4:17854289
|
C | T | 64 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0003g0214others(61): Show | 65 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.5603-8388G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17854289 | ||||||
| chr4:17854684
|
T | TA | 9 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.5603-8784dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17854684 | ||||||
| chr4:17854868
|
A | G | 1 | a0019c0019t0010g0221 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5603-8967T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17854868 | ||||||
| chr4:17855074
|
C | T | 73 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0009g0129others(70): Show | 74 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.5603-9173G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17855074 | ||||||
| chr4:17855178
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(185): Show | 190 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.5603-9277G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17855178 | ||||||
| chr4:17855204
|
C | T | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5603-9303G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17855204 | ||||||
| chr4:17855435
|
C | T | 1 | a0011c0028t0001g0137 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.5603-9534G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17855435 | ||||||
| chr4:17855630
|
A | G | 58 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(55): Show | 59 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.5603-9729T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17855630 | ||||||
| chr4:17855648
|
T | C | 2 | a0001c0003t0003g0215a0001c0003t0003g0245 | 2 | NA19005.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.5603-9747A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17855648 | ||||||
| chr4:17856109
|
A | G | 1 | a0001c0001t0010g0226 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5603-10208T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17856109 | ||||||
| chr4:17856783
|
T | C | 1 | a0019c0019t0010g0221 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5603-10882A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17856783 | ||||||
| chr4:17856983
|
C | T | 6 | a0006c0007t0006g0250a0006c0007t0006g0272a0006c0007t0006g0274others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.5603-11082G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17856983 | ||||||
| chr4:17857268
|
G | A | 2 | a0002c0002t0002g0027a0002c0002t0002g0069 | 2 | NA19007.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.5603-11367C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17857268 | ||||||
| chr4:17857307
|
A | G | 1 | a0001c0001t0019g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5603-11406T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17857307 | ||||||
| chr4:17857340
|
A | C | 3 | a0001c0003t0003g0236a0001c0003t0003g0237a0001c0003t0003g0258 | 3 | HG01243.hp2 HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.5603-11439T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17857340 | ||||||
| chr4:17857517
|
A | G | 13 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(10): Show | 13 | HG00423.hp2 HG00438.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.5603-11616T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17857517 | ||||||
| chr4:17857843
|
A | G | 58 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(55): Show | 59 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.5603-11942T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17857843 | ||||||
| chr4:17857880
|
G | C | 2 | a0001c0001t0019g0133a0001c0001t0019g0204 | 2 | HG02717.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.5603-11979C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17857880 | ||||||
| chr4:17858145
|
C | T | 79 | a0001c0001t0002g0025a0001c0001t0002g0046a0001c0001t0002g0049others(76): Show | 79 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.5603-12244G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858145 | ||||||
| chr4:17858203
|
C | T | 1 | a0001c0001t0010g0226 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5603-12302G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858203 | ||||||
| chr4:17858210
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5603-12309G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858210 | ||||||
| chr4:17858323
|
GA | G | 41 | a0001c0001t0009g0173a0001c0003t0003g0214a0001c0003t0003g0215others(38): Show | 42 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.5603-12423delT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858323 | ||||||
| chr4:17858558
|
T | TA | 7 | a0001c0001t0001g0159a0006c0007t0006g0250a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.5603-12658dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858558 | ||||||
| chr4:17858598
|
C | G | 2 | a0004c0005t0008g0280a0004c0005t0008g0281 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.5603-12697G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858598 | ||||||
| chr4:17858729
|
A | AAAT | 13 | a0001c0001t0001g0163a0001c0003t0003g0233a0001c0003t0003g0234others(10): Show | 13 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.5603-12831_5603-12 others(9): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858729 | ||||||
| chr4:17858729
|
A | AAATAAT | 12 | a0001c0001t0023g0007a0001c0003t0003g0240a0001c0003t0003g0246others(9): Show | 13 | HG00423.hp1 HG01515.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.5603-12834_5603-12 others(12): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858729 | ||||||
| chr4:17858729
|
A | AAATAATA others(2): Show |
4 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0229others(1): Show | 4 | HG02145.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.5603-12837_5603-12 others(15): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858729 | ||||||
| chr4:17858729
|
A | AAATAATA others(8): Show |
3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5603-12843_5603-12 others(21): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858729 | ||||||
| chr4:17858956
|
A | G | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.5603-13055T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17858956 | ||||||
| chr4:17859121
|
T | C | 1 | a0004c0005t0030g0290 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5603-13220A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17859121 | ||||||
| chr4:17859146
|
A | T | 1 | a0019c0019t0010g0221 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5603-13245T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17859146 | ||||||
| chr4:17859197
|
C | T | 198 | a0001c0001t0002g0025a0001c0001t0002g0046a0001c0001t0002g0049others(195): Show | 199 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.5603-13296G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17859197 | ||||||
| chr4:17859305
|
T | A | 7 | a0001c0001t0023g0007a0005c0006t0005g0231a0005c0006t0011g0208others(4): Show | 7 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.5603-13404A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17859305 | ||||||
| chr4:17859431
|
A | C | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5603-13530T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17859431 | ||||||
| chr4:17859587
|
T | C | 71 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0023g0007others(68): Show | 72 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.5603-13686A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17859587 | ||||||
| chr4:17859919
|
G | A | 1 | a0003c0004t0004g0097 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5602+13469C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17859919 | ||||||
| chr4:17860052
|
T | C | 1 | a0001c0003t0003g0254 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5602+13336A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17860052 | ||||||
| chr4:17860102
|
G | C | 9 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.5602+13286C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17860102 | ||||||
| chr4:17860169
|
G | A | 1 | a0003c0004t0004g0107 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.5602+13219C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17860169 | ||||||
| chr4:17860533
|
T | G | 3 | a0006c0007t0006g0274a0006c0007t0006g0277a0006c0007t0006g0278 | 3 | HG02451.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.5602+12855A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17860533 | ||||||
| chr4:17860695
|
C | T | 16 | a0003c0004t0004g0094a0003c0004t0004g0096a0003c0004t0004g0097others(13): Show | 16 | HG00673.hp1 HG02602.hp2 HG03017.hp1 others(13): Show |
intron_variant | MODIFIER | c.5602+12693G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17860695 | ||||||
| chr4:17860771
|
T | C | 1 | a0002c0002t0002g0080 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.5602+12617A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17860771 | ||||||
| chr4:17860876
|
G | A | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5602+12512C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17860876 | ||||||
| chr4:17861037
|
G | A | 2 | a0005c0006t0011g0222a0005c0006t0011g0223 | 2 | HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.5602+12351C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861037 | ||||||
| chr4:17861203
|
T | C | 13 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(10): Show | 13 | HG01081.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.5602+12185A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861203 | ||||||
| chr4:17861316
|
C | A | 1 | a0001c0003t0003g0260 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5602+12072G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861316 | ||||||
| chr4:17861379
|
C | T | 13 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(10): Show | 13 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.5602+12009G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861379 | ||||||
| chr4:17861445
|
C | T | 1 | a0002c0002t0038g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5602+11943G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861445 | ||||||
| chr4:17861486
|
T | C | 1 | a0001c0001t0002g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5602+11902A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861486 | ||||||
| chr4:17861569
|
T | G | 1 | a0001c0003t0003g0241 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.5602+11819A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861569 | ||||||
| chr4:17861614
|
G | A | 9 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(6): Show | 9 | HG00423.hp2 HG00438.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.5602+11774C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861614 | ||||||
| chr4:17861775
|
C | T | 3 | a0001c0001t0001g0136a0001c0001t0001g0207a0002c0002t0005g0112 | 3 | HG02615.hp2 NA18991.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.5602+11613G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861775 | ||||||
| chr4:17861835
|
G | T | 61 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0003g0214others(58): Show | 62 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.5602+11553C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861835 | ||||||
| chr4:17861909
|
T | C | 1 | a0002c0002t0002g0084 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.5602+11479A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17861909 | ||||||
| chr4:17862003
|
C | G | 1 | a0011c0028t0001g0137 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.5602+11385G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862003 | ||||||
| chr4:17862052
|
C | T | 4 | a0003c0004t0004g0099a0003c0004t0004g0101a0003c0004t0004g0103others(1): Show | 4 | NA18941.hp1 NA18949.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.5602+11336G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862052 | ||||||
| chr4:17862057
|
C | T | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.5602+11331G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862057 | ||||||
| chr4:17862069
|
T | C | 1 | a0001c0001t0016g0140 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.5602+11319A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862069 | ||||||
| chr4:17862170
|
T | C | 2 | a0013c0013t0002g0073a0013c0013t0002g0074 | 2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.5602+11218A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862170 | ||||||
| chr4:17862391
|
T | C | 96 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0009g0129others(93): Show | 97 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.5602+10997A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862391 | ||||||
| chr4:17862433
|
C | T | 2 | a0014c0011t0004g0092a0014c0011t0004g0093 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5602+10955G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862433 | ||||||
| chr4:17862454
|
T | C | 10 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.5602+10934A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862454 | ||||||
| chr4:17862622
|
A | T | 10 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(7): Show | 10 | HG02055.hp2 HG02145.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.5602+10766T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862622 | ||||||
| chr4:17862651
|
T | C | 58 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0003g0214others(55): Show | 59 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.5602+10737A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862651 | ||||||
| chr4:17862691
|
G | A | 1 | a0004c0005t0008g0286 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.5602+10697C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862691 | ||||||
| chr4:17862731
|
G | C | 3 | a0014c0011t0004g0092a0014c0011t0004g0093a0023c0016t0004g0091 | 3 | HG02630.hp2 HG03139.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5602+10657C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862731 | ||||||
| chr4:17862818
|
A | C | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5602+10570T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862818 | ||||||
| chr4:17862843
|
G | GT | 13 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(10): Show | 13 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.5602+10544_5602+10 others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862843 | ||||||
| chr4:17862844
|
C | A | 13 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(10): Show | 13 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.5602+10544G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862844 | ||||||
| chr4:17862990
|
T | TATAAC | 96 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0009g0129others(93): Show | 97 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.5602+10397_5602+10 others(11): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17862990 | ||||||
| chr4:17863118
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.5602+10270G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17863118 | ||||||
| chr4:17863290
|
TG | T | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5602+10097delC | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17863290 | ||||||
| chr4:17863617
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5602+9771G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17863617 | ||||||
| chr4:17863915
|
A | T | 13 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(10): Show | 13 | HG01081.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.5602+9473T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17863915 | ||||||
| chr4:17863938
|
G | A | 55 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(52): Show | 56 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.5602+9450C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17863938 | ||||||
| chr4:17864093
|
C | T | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5602+9295G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17864093 | ||||||
| chr4:17864241
|
T | A | 34 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(31): Show | 35 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.5602+9147A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17864241 | ||||||
| chr4:17864242
|
T | A | 64 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0023g0007others(61): Show | 65 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.5602+9146A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17864242 | ||||||
| chr4:17864489
|
G | A | 81 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(78): Show | 82 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(79): Show |
intron_variant | MODIFIER | c.5602+8899C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17864489 | ||||||
| chr4:17864561
|
T | C | 8 | a0001c0001t0023g0007a0005c0006t0005g0231a0005c0006t0011g0208others(5): Show | 8 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.5602+8827A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17864561 | ||||||
| chr4:17864661
|
A | C | 1 | a0002c0002t0038g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5602+8727T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17864661 | ||||||
| chr4:17864702
|
G | A | 64 | a0001c0001t0002g0025a0001c0001t0023g0007a0001c0001t0029g0232others(61): Show | 65 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.5602+8686C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17864702 | ||||||
| chr4:17864932
|
G | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.5602+8456C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17864932 | ||||||
| chr4:17864970
|
A | C | 3 | a0002c0002t0014g0211a0002c0002t0014g0212a0002c0002t0014g0213 | 3 | HG01891.hp2 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.5602+8418T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17864970 | ||||||
| chr4:17865158
|
A | G | 2 | a0001c0003t0003g0215a0001c0003t0003g0245 | 2 | NA19005.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.5602+8230T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17865158 | ||||||
| chr4:17865243
|
C | T | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.5602+8145G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17865243 | ||||||
| chr4:17865295
|
G | A | 1 | a0001c0001t0019g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5602+8093C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17865295 | ||||||
| chr4:17865335
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.5602+8053A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17865335 | ||||||
| chr4:17865415
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(87): Show | 91 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.5602+7973T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17865415 | ||||||
| chr4:17865790
|
G | A | 1 | a0019c0019t0010g0221 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5602+7598C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17865790 | ||||||
| chr4:17865913
|
G | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5602+7475C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17865913 | ||||||
| chr4:17866241
|
C | A | 3 | a0003c0004t0004g0099a0003c0004t0004g0101a0003c0004t0004g0103 | 3 | NA18941.hp1 NA18959.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.5602+7147G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17866241 | ||||||
| chr4:17866289
|
C | T | 1 | a0001c0001t0012g0082 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.5602+7099G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17866289 | ||||||
| chr4:17866408
|
C | T | 1 | a0002c0002t0002g0009 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.5602+6980G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17866408 | ||||||
| chr4:17866411
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5602+6977A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17866411 | ||||||
| chr4:17866435
|
T | C | 65 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0003g0214others(62): Show | 66 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.5602+6953A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17866435 | ||||||
| chr4:17866462
|
C | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5602+6926G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17866462 | ||||||
| chr4:17867173
|
T | A | 1 | a0020c0023t0002g0005 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5602+6215A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17867173 | ||||||
| chr4:17867611
|
T | C | 22 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(19): Show | 22 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(19): Show |
intron_variant | MODIFIER | c.5602+5777A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17867611 | ||||||
| chr4:17868005
|
G | GA | 3 | a0002c0002t0002g0009a0002c0002t0002g0034a0002c0002t0002g0047 | 3 | NA18944.hp1 NA18946.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.5602+5382_5602+538 others(5): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17868005 | ||||||
| chr4:17868006
|
T | C | 16 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.5602+5382A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17868006 | ||||||
| chr4:17868196
|
C | A | 4 | a0004c0024t0013g0088a0007c0008t0013g0217a0007c0008t0013g0218others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.5602+5192G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17868196 | ||||||
| chr4:17868522
|
C | A | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.5602+4866G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17868522 | ||||||
| chr4:17868656
|
T | C | 13 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(10): Show | 13 | HG01081.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.5602+4732A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17868656 | ||||||
| chr4:17868791
|
G | A | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5602+4597C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17868791 | ||||||
| chr4:17868942
|
A | T | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.5602+4446T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17868942 | ||||||
| chr4:17869044
|
C | CT | 60 | a0001c0001t0002g0065a0001c0003t0001g0239a0001c0003t0003g0214others(57): Show | 61 | HG00423.hp1 HG00673.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.5602+4343dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17869044 | ||||||
| chr4:17869044
|
CTT | C | 23 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(20): Show | 23 | HG01358.hp2 HG01891.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.5602+4342_5602+434 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17869044 | ||||||
| chr4:17869152
|
A | G | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.5602+4236T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17869152 | ||||||
| chr4:17869338
|
CTTCAT | C | 7 | a0002c0002t0002g0006a0002c0002t0002g0043a0002c0002t0002g0044others(4): Show | 7 | HG01074.hp2 HG01258.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.5602+4045_5602+404 others(9): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17869338 | ||||||
| chr4:17869389
|
C | G | 65 | a0001c0001t0002g0025a0001c0001t0002g0046a0001c0001t0002g0049others(62): Show | 65 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.5602+3999G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17869389 | ||||||
| chr4:17869580
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0188 | 2 | HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.5602+3808A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17869580 | ||||||
| chr4:17869679
|
A | G | 2 | a0002c0002t0002g0004a0002c0002t0033g0070 | 2 | NA18986.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.5602+3709T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17869679 | ||||||
| chr4:17869749
|
G | A | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5602+3639C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17869749 | ||||||
| chr4:17870157
|
T | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5602+3231A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17870157 | ||||||
| chr4:17870176
|
T | C | 26 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.5602+3212A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17870176 | ||||||
| chr4:17870299
|
C | T | 1 | a0001c0003t0003g0263 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5602+3089G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17870299 | ||||||
| chr4:17870461
|
C | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5602+2927G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17870461 | ||||||
| chr4:17870548
|
T | C | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5602+2840A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17870548 | ||||||
| chr4:17870717
|
T | G | 1 | a0003c0004t0004g0099 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.5602+2671A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17870717 | ||||||
| chr4:17870751
|
TGC | T | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.5602+2635_5602+263 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17870751 | ||||||
| chr4:17870766
|
T | C | 17 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(14): Show | 17 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.5602+2622A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17870766 | ||||||
| chr4:17870941
|
T | C | 2 | a0001c0001t0017g0199a0004c0005t0008g0287 | 2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5602+2447A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17870941 | ||||||
| chr4:17871084
|
T | C | 42 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(39): Show | 43 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.5602+2304A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17871084 | ||||||
| chr4:17871243
|
TA | T | 5 | a0001c0001t0001g0134a0001c0001t0001g0151a0001c0001t0001g0153others(2): Show | 5 | HG01192.hp1 NA18985.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.5602+2144delT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17871243 | ||||||
| chr4:17871869
|
A | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5602+1519T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17871869 | ||||||
| chr4:17872069
|
AGAG | A | 42 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(39): Show | 43 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.5602+1316_5602+131 others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17872069 | ||||||
| chr4:17872290
|
C | T | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.5602+1098G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17872290 | ||||||
| chr4:17872457
|
C | T | 1 | a0002c0002t0012g0035 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.5602+931G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17872457 | ||||||
| chr4:17872466
|
C | T | 70 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0001g0239others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.5602+922G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17872466 | ||||||
| chr4:17872481
|
C | T | 1 | a0002c0002t0002g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.5602+907G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17872481 | ||||||
| chr4:17872532
|
C | T | 9 | a0001c0003t0003g0215a0001c0003t0003g0233a0001c0003t0003g0234others(6): Show | 9 | HG00735.hp1 HG00738.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.5602+856G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17872532 | ||||||
| chr4:17872576
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.5602+812C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17872576 | ||||||
| chr4:17873012
|
T | C | 25 | a0001c0001t0001g0200a0003c0004t0002g0109a0003c0004t0004g0094others(22): Show | 25 | HG00673.hp1 HG01109.hp1 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.5602+376A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17873012 | ||||||
| chr4:17873193
|
T | C | 1 | a0001c0001t0007g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5602+195A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 7/7 | chr4 | 17873193 | ||||||
| chr4:17878365
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.777-152C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17878365 | ||||||
| chr4:17878373
|
A | C | 16 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.777-160T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17878373 | ||||||
| chr4:17878403
|
G | A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.777-190C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17878403 | ||||||
| chr4:17878481
|
T | C | 2 | a0002c0002t0002g0022a0002c0002t0002g0023 | 2 | NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.777-268A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17878481 | ||||||
| chr4:17878768
|
T | A | 1 | a0002c0002t0002g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.777-555A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17878768 | ||||||
| chr4:17878793
|
A | C | 63 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0001g0239others(60): Show | 64 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.777-580T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17878793 | ||||||
| chr4:17878849
|
T | A | 3 | a0002c0002t0002g0030a0002c0002t0002g0032a0002c0002t0002g0033 | 3 | NA18943.hp1 NA18949.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.777-636A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17878849 | ||||||
| chr4:17879083
|
T | C | 1 | a0002c0002t0038g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.777-870A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879083 | ||||||
| chr4:17879158
|
T | C | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.777-945A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879158 | ||||||
| chr4:17879171
|
T | TTC | 32 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(29): Show | 32 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.777-959_777-958ins others(2): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879171 | ||||||
| chr4:17879244
|
A | G | 1 | a0002c0002t0034g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.777-1031T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879244 | ||||||
| chr4:17879270
|
C | T | 26 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.777-1057G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879270 | ||||||
| chr4:17879391
|
C | G | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.777-1178G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879391 | ||||||
| chr4:17879410
|
T | C | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.777-1197A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879410 | ||||||
| chr4:17879534
|
C | T | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.777-1321G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879534 | ||||||
| chr4:17879545
|
T | C | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.777-1332A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879545 | ||||||
| chr4:17879553
|
G | A | 3 | a0001c0003t0003g0244a0001c0003t0003g0256a0001c0003t0003g0261 | 3 | HG02027.hp1 HG02083.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.777-1340C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879553 | ||||||
| chr4:17879572
|
C | T | 32 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(29): Show | 32 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.777-1359G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879572 | ||||||
| chr4:17879594
|
A | G | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.777-1381T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879594 | ||||||
| chr4:17879693
|
T | C | 1 | a0002c0002t0002g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.777-1480A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879693 | ||||||
| chr4:17879862
|
T | C | 32 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(29): Show | 32 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.777-1649A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17879862 | ||||||
| chr4:17880065
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.777-1852A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17880065 | ||||||
| chr4:17880108
|
G | A | 1 | a0001c0003t0003g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.777-1895C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17880108 | ||||||
| chr4:17880131
|
G | A | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.777-1918C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17880131 | ||||||
| chr4:17880210
|
T | A | 16 | a0004c0024t0013g0088a0005c0006t0005g0231a0005c0006t0011g0208others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.777-1997A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17880210 | ||||||
| chr4:17880288
|
A | G | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.777-2075T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17880288 | ||||||
| chr4:17880529
|
A | G | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.777-2316T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17880529 | ||||||
| chr4:17880623
|
T | C | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.777-2410A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17880623 | ||||||
| chr4:17881249
|
C | T | 6 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0222others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.777-3036G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17881249 | ||||||
| chr4:17881338
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | NA18950.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.777-3125A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17881338 | ||||||
| chr4:17881572
|
A | C | 1 | a0002c0026t0005g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.777-3359T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17881572 | ||||||
| chr4:17881737
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.777-3524A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17881737 | ||||||
| chr4:17881851
|
T | C | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.777-3638A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17881851 | ||||||
| chr4:17881980
|
G | GA | 63 | a0001c0001t0009g0166a0001c0003t0001g0239a0001c0003t0003g0214others(60): Show | 64 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.777-3768dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17881980 | ||||||
| chr4:17882060
|
G | C | 8 | a0002c0002t0002g0024a0002c0002t0002g0038a0002c0002t0002g0060others(5): Show | 8 | HG00642.hp1 HG01069.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.777-3847C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17882060 | ||||||
| chr4:17882162
|
G | A | 2 | a0004c0005t0008g0286a0004c0005t0008g0288 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.776+3906C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17882162 | ||||||
| chr4:17882235
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.776+3833A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17882235 | ||||||
| chr4:17882439
|
C | T | 1 | a0001c0001t0018g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.776+3629G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17882439 | ||||||
| chr4:17882483
|
T | G | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.776+3585A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17882483 | ||||||
| chr4:17882530
|
A | G | 1 | a0002c0002t0002g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.776+3538T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17882530 | ||||||
| chr4:17882925
|
C | G | 4 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0229others(1): Show | 4 | HG02145.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+3143G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17882925 | ||||||
| chr4:17883146
|
G | A | 10 | a0004c0024t0013g0088a0006c0007t0006g0250a0006c0007t0006g0272others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.776+2922C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883146 | ||||||
| chr4:17883297
|
T | A | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.776+2771A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883297 | ||||||
| chr4:17883363
|
T | C | 65 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0006g0121others(62): Show | 66 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.776+2705A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883363 | ||||||
| chr4:17883673
|
A | AAC | 169 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(166): Show | 171 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.776+2393_776+2394d others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883673 | ||||||
| chr4:17883673
|
A | AACAC | 19 | a0004c0005t0008g0282a0004c0005t0008g0286a0004c0005t0008g0287others(16): Show | 19 | HG02145.hp1 HG02145.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.776+2391_776+2394d others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883673 | ||||||
| chr4:17883673
|
A | AACACAC | 4 | a0004c0005t0008g0283a0006c0007t0006g0274a0006c0007t0006g0277others(1): Show | 4 | HG02451.hp1 HG03209.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.776+2389_776+2394d others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883673 | ||||||
| chr4:17883673
|
A | AC | 4 | a0001c0001t0001g0180a0001c0001t0007g0016a0001c0001t0010g0226others(1): Show | 4 | HG02896.hp1 HG02896.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+2394_776+2395i others(3): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883673 | ||||||
| chr4:17883694
|
T | A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.776+2374A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883694 | ||||||
| chr4:17883698
|
A | T | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.776+2370T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883698 | ||||||
| chr4:17883699
|
A | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.776+2369T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883699 | ||||||
| chr4:17883723
|
C | T | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.776+2345G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17883723 | ||||||
| chr4:17884363
|
TTCTGTAG others(55): Show |
T | 1 | a0001c0001t0001g0159 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.776+1643_776+1704d others(64): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17884363 | ||||||
| chr4:17884523
|
A | G | 5 | a0001c0001t0001g0135a0001c0001t0001g0195a0008c0010t0001g0189others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.776+1545T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17884523 | ||||||
| chr4:17885132
|
T | G | 1 | a0002c0002t0002g0072 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.776+936A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17885132 | ||||||
| chr4:17885414
|
G | A | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.776+654C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17885414 | ||||||
| chr4:17885507
|
T | TA | 12 | a0004c0005t0004g0220a0004c0024t0013g0088a0005c0006t0005g0231others(9): Show | 12 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.776+560dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17885507 | ||||||
| chr4:17885507
|
T | TAA | 6 | a0006c0007t0006g0250a0006c0007t0006g0272a0006c0007t0006g0274others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+559_776+560dup others(2): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17885507 | ||||||
| chr4:17885508
|
A | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(85): Show | 89 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.776+560T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17885508 | ||||||
| chr4:17885587
|
A | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.776+481T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17885587 | ||||||
| chr4:17885645
|
A | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.776+423T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17885645 | ||||||
| chr4:17886064
|
T | TTACCCAG others(54): Show |
1 | a0001c0001t0001g0159 | 1 | NA19007.hp2 | splice_region_variant&intron_variant | LOW | c.719_776+3dupGCATAA others(55): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 6/7 | chr4 | 17886064 | ||||||
| chr4:17886177
|
G | C | 1 | a0002c0002t0002g0042 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.683-16C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17886177 | ||||||
| chr4:17886732
|
G | A | 11 | a0004c0024t0013g0088a0006c0007t0006g0250a0006c0007t0006g0272others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.683-571C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17886732 | ||||||
| chr4:17886923
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.683-762T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17886923 | ||||||
| chr4:17886926
|
C | A | 2 | a0001c0003t0003g0246a0001c0003t0003g0249 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.683-765G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17886926 | ||||||
| chr4:17887165
|
C | T | 10 | a0001c0003t0003g0214a0001c0003t0003g0238a0001c0003t0003g0244others(7): Show | 10 | HG00639.hp1 HG01192.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-1004G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17887165 | ||||||
| chr4:17887526
|
G | T | 3 | a0002c0002t0002g0019a0002c0002t0034g0015a0002c0002t0038g0013 | 3 | HG02809.hp2 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.683-1365C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17887526 | ||||||
| chr4:17887722
|
A | G | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.683-1561T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17887722 | ||||||
| chr4:17887782
|
C | T | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.683-1621G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17887782 | ||||||
| chr4:17888166
|
A | T | 1 | a0002c0002t0002g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.683-2005T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17888166 | ||||||
| chr4:17888414
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.683-2253G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17888414 | ||||||
| chr4:17888605
|
A | T | 13 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(10): Show | 13 | HG01081.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.683-2444T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17888605 | ||||||
| chr4:17888674
|
T | A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.683-2513A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17888674 | ||||||
| chr4:17888931
|
C | T | 1 | a0016c0029t0006g0285 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.683-2770G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17888931 | ||||||
| chr4:17888932
|
C | T | 1 | a0019c0019t0010g0221 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.683-2771G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17888932 | ||||||
| chr4:17889027
|
T | A | 1 | a0001c0001t0019g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.683-2866A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889027 | ||||||
| chr4:17889155
|
C | T | 5 | a0001c0001t0001g0135a0001c0001t0001g0195a0008c0010t0001g0189others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-2994G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889155 | ||||||
| chr4:17889308
|
C | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.683-3147G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889308 | ||||||
| chr4:17889337
|
A | G | 43 | a0001c0001t0001g0154a0001c0003t0001g0239a0001c0003t0003g0214others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.683-3176T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889337 | ||||||
| chr4:17889434
|
G | A | 5 | a0001c0001t0001g0135a0001c0001t0001g0195a0008c0010t0001g0189others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-3273C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889434 | ||||||
| chr4:17889499
|
T | C | 1 | a0002c0002t0034g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.683-3338A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889499 | ||||||
| chr4:17889542
|
G | A | 1 | a0002c0002t0033g0070 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.683-3381C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889542 | ||||||
| chr4:17889656
|
T | C | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.683-3495A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889656 | ||||||
| chr4:17889737
|
T | C | 1 | a0002c0002t0002g0037 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.683-3576A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889737 | ||||||
| chr4:17889952
|
A | G | 1 | a0001c0001t0009g0129 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.683-3791T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17889952 | ||||||
| chr4:17890028
|
G | A | 3 | a0008c0010t0001g0189a0008c0010t0001g0190a0008c0010t0001g0197 | 3 | HG01069.hp1 HG01071.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.683-3867C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890028 | ||||||
| chr4:17890211
|
T | C | 2 | a0002c0002t0002g0055a0002c0002t0002g0056 | 2 | HG02083.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.683-4050A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890211 | ||||||
| chr4:17890248
|
G | A | 1 | a0002c0002t0035g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.683-4087C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890248 | ||||||
| chr4:17890299
|
T | C | 3 | a0001c0001t0001g0154a0001c0003t0003g0266a0001c0003t0003g0271 | 3 | HG01099.hp2 HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.683-4138A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890299 | ||||||
| chr4:17890407
|
G | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0131 | 2 | HG01433.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.683-4246C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890407 | ||||||
| chr4:17890610
|
G | A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.683-4449C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890610 | ||||||
| chr4:17890659
|
C | T | 1 | a0002c0002t0002g0028 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.683-4498G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890659 | ||||||
| chr4:17890741
|
G | A | 43 | a0001c0001t0001g0154a0001c0003t0001g0239a0001c0003t0003g0214others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.683-4580C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890741 | ||||||
| chr4:17890777
|
T | G | 45 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0006g0121others(42): Show | 46 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.683-4616A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890777 | ||||||
| chr4:17890828
|
G | GTTAA | 63 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0006g0121others(60): Show | 64 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.683-4668_683-4667i others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17890828 | ||||||
| chr4:17891280
|
C | T | 1 | a0002c0002t0012g0051 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.683-5119G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17891280 | ||||||
| chr4:17891573
|
C | T | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.683-5412G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17891573 | ||||||
| chr4:17891588
|
T | C | 1 | a0001c0003t0003g0252 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.683-5427A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17891588 | ||||||
| chr4:17891991
|
A | G | 1 | a0001c0001t0002g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.683-5830T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17891991 | ||||||
| chr4:17892017
|
T | G | 1 | a0001c0003t0003g0254 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.683-5856A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892017 | ||||||
| chr4:17892197
|
AT | A | 19 | a0001c0001t0001g0132a0001c0001t0001g0147a0001c0001t0001g0176others(16): Show | 19 | HG01099.hp1 HG02622.hp2 HG02683.hp1 others(16): Show |
intron_variant | MODIFIER | c.683-6037delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892197 | ||||||
| chr4:17892203
|
T | TTC | 18 | a0004c0005t0004g0220a0004c0024t0013g0088a0005c0006t0005g0231others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.683-6043_683-6042i others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892203 | ||||||
| chr4:17892208
|
T | C | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.683-6047A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892208 | ||||||
| chr4:17892209
|
C | T | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.683-6048G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892209 | ||||||
| chr4:17892437
|
G | A | 2 | a0002c0002t0020g0275a0002c0002t0020g0276 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.683-6276C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892437 | ||||||
| chr4:17892616
|
T | TAA | 18 | a0004c0005t0004g0220a0004c0024t0013g0088a0005c0006t0005g0231others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.683-6456_683-6455i others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892616 | ||||||
| chr4:17892647
|
T | C | 3 | a0006c0007t0006g0274a0006c0007t0006g0277a0006c0007t0006g0278 | 3 | HG02451.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.683-6486A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892647 | ||||||
| chr4:17892780
|
A | T | 1 | a0001c0001t0009g0129 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.683-6619T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892780 | ||||||
| chr4:17892857
|
T | TGTTCTCT others(359): Show |
1 | a0003c0004t0004g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.683-6697_683-6696i others(368): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17892857 | ||||||
| chr4:17893207
|
A | G | 18 | a0004c0005t0004g0220a0004c0024t0013g0088a0005c0006t0005g0231others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.683-7046T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893207 | ||||||
| chr4:17893227
|
A | G | 18 | a0004c0005t0004g0220a0004c0024t0013g0088a0005c0006t0005g0231others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.683-7066T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893227 | ||||||
| chr4:17893257
|
T | C | 5 | a0001c0003t0025g0264a0004c0005t0008g0286a0004c0005t0008g0287others(2): Show | 5 | HG01074.hp1 HG02615.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-7096A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893257 | ||||||
| chr4:17893264
|
T | C | 1 | a0001c0003t0003g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.683-7103A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893264 | ||||||
| chr4:17893307
|
C | T | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.683-7146G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893307 | ||||||
| chr4:17893362
|
T | C | 1 | a0002c0002t0002g0029 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.683-7201A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893362 | ||||||
| chr4:17893415
|
G | A | 1 | a0002c0002t0005g0112 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.683-7254C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893415 | ||||||
| chr4:17893644
|
T | C | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.683-7483A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893644 | ||||||
| chr4:17893850
|
G | A | 18 | a0004c0005t0004g0220a0004c0024t0013g0088a0005c0006t0005g0231others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.683-7689C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893850 | ||||||
| chr4:17893884
|
T | C | 8 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(5): Show | 8 | HG00423.hp2 HG00438.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.683-7723A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893884 | ||||||
| chr4:17893901
|
C | T | 1 | a0006c0007t0006g0272 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.683-7740G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17893901 | ||||||
| chr4:17894079
|
G | A | 2 | a0002c0002t0002g0080a0002c0002t0002g0081 | 2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.683-7918C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894079 | ||||||
| chr4:17894249
|
T | C | 18 | a0004c0005t0004g0220a0004c0024t0013g0088a0005c0006t0005g0231others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.683-8088A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894249 | ||||||
| chr4:17894356
|
A | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.683-8195T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894356 | ||||||
| chr4:17894416
|
T | C | 1 | a0004c0005t0008g0288 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.683-8255A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894416 | ||||||
| chr4:17894543
|
G | T | 6 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0222others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-8382C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894543 | ||||||
| chr4:17894623
|
C | T | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.683-8462G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894623 | ||||||
| chr4:17894643
|
C | T | 1 | a0006c0007t0006g0250 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.683-8482G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894643 | ||||||
| chr4:17894816
|
A | G | 1 | a0022c0022t0016g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.683-8655T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894816 | ||||||
| chr4:17894824
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.683-8663A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894824 | ||||||
| chr4:17894851
|
A | G | 7 | a0001c0001t0001g0059a0001c0001t0001g0145a0001c0001t0001g0155others(4): Show | 7 | NA18955.hp1 NA18956.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.683-8690T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894851 | ||||||
| chr4:17894952
|
C | G | 43 | a0001c0001t0001g0154a0001c0003t0001g0239a0001c0003t0003g0214others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.683-8791G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17894952 | ||||||
| chr4:17895030
|
T | C | 1 | a0002c0002t0002g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.683-8869A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895030 | ||||||
| chr4:17895042
|
A | T | 1 | a0002c0002t0002g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.683-8881T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895042 | ||||||
| chr4:17895095
|
A | C | 26 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.683-8934T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895095 | ||||||
| chr4:17895186
|
A | C | 3 | a0009c0009t0001g0178a0009c0009t0001g0186a0009c0009t0001g0187 | 3 | HG02056.hp2 NA18948.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.683-9025T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895186 | ||||||
| chr4:17895226
|
T | C | 1 | a0001c0001t0023g0007 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.683-9065A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895226 | ||||||
| chr4:17895260
|
C | A | 3 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224 | 3 | HG02896.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.683-9099G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895260 | ||||||
| chr4:17895400
|
C | T | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.683-9239G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895400 | ||||||
| chr4:17895429
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.683-9268T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895429 | ||||||
| chr4:17895430
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.683-9269G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895430 | ||||||
| chr4:17895692
|
C | T | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.683-9531G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895692 | ||||||
| chr4:17895710
|
C | T | 1 | a0001c0003t0003g0258 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.683-9549G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895710 | ||||||
| chr4:17895790
|
A | G | 3 | a0001c0003t0003g0238a0001c0003t0003g0251a0001c0003t0003g0253 | 3 | HG00639.hp1 HG01192.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.683-9629T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895790 | ||||||
| chr4:17895812
|
T | C | 10 | a0004c0024t0013g0088a0006c0007t0006g0250a0006c0007t0006g0272others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-9651A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895812 | ||||||
| chr4:17895888
|
T | A | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.683-9727A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895888 | ||||||
| chr4:17895981
|
T | C | 1 | a0002c0002t0005g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.683-9820A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17895981 | ||||||
| chr4:17896136
|
C | A | 1 | a0002c0002t0002g0030 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.683-9975G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17896136 | ||||||
| chr4:17896178
|
TC | T | 3 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224 | 3 | HG02896.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.683-10018delG | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17896178 | ||||||
| chr4:17896249
|
T | G | 1 | a0001c0003t0003g0247 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.683-10088A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17896249 | ||||||
| chr4:17896875
|
C | G | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.683-10714G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17896875 | ||||||
| chr4:17897013
|
T | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.683-10852A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897013 | ||||||
| chr4:17897206
|
C | T | 19 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(16): Show | 19 | HG01081.hp2 HG01358.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-11045G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897206 | ||||||
| chr4:17897212
|
T | TC | 59 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0122others(56): Show | 60 | HG00642.hp1 HG00642.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.683-11052dupG | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897212 | ||||||
| chr4:17897213
|
C | CCT | 34 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0123others(31): Show | 34 | HG00423.hp2 HG00673.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.683-11053_683-1105 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
C | CCTT | 18 | a0001c0001t0001g0068a0001c0001t0001g0135a0001c0001t0001g0150others(15): Show | 18 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.683-11053_683-1105 others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
C | CCTTT | 7 | a0001c0001t0002g0065a0002c0002t0002g0069a0002c0002t0002g0077others(4): Show | 7 | HG02056.hp2 HG02698.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.683-11053_683-1105 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
C | CCTTTT | 6 | a0001c0001t0002g0025a0001c0001t0012g0062a0002c0002t0002g0019others(3): Show | 6 | HG00438.hp2 HG02809.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-11053_683-1105 others(9): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
CT | C | 15 | a0001c0001t0007g0014a0001c0001t0007g0021a0001c0001t0010g0226others(12): Show | 15 | HG01175.hp2 HG01346.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.683-11053delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
CTT | C | 17 | a0001c0001t0007g0017a0001c0003t0003g0215a0001c0003t0003g0216others(14): Show | 17 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.683-11054_683-1105 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
CTTT | C | 18 | a0001c0003t0003g0214a0001c0003t0003g0240a0001c0003t0003g0244others(15): Show | 19 | HG00423.hp1 HG00639.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-11055_683-1105 others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0005g0114a0002c0002t0014g0212a0004c0024t0013g0088others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-11062_683-1105 others(14): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
CTTTTTTT others(4): Show |
C | 23 | a0002c0002t0005g0111a0002c0002t0005g0112a0002c0002t0005g0113others(20): Show | 23 | HG01081.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.683-11063_683-1105 others(15): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
CTTTTTTT others(5): Show |
C | 16 | a0001c0003t0003g0262a0001c0003t0003g0263a0002c0002t0002g0083others(13): Show | 16 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-11064_683-1105 others(16): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
CTTTTTTT others(6): Show |
C | 1 | a0004c0005t0031g0284 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.683-11065_683-1105 others(17): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0192a0001c0001t0001g0201a0002c0002t0002g0064others(1): Show | 4 | HG02622.hp2 HG03239.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-11068_683-1105 others(20): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897213
|
CTTTTTTT others(10): Show |
C | 16 | a0003c0004t0004g0094a0003c0004t0004g0096a0003c0004t0004g0097others(13): Show | 16 | HG00673.hp1 HG02602.hp2 HG03017.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-11069_683-1105 others(21): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897213 | ||||||
| chr4:17897214
|
T | C | 37 | a0001c0001t0001g0124a0001c0001t0001g0160a0001c0001t0001g0185others(34): Show | 37 | HG00639.hp2 HG00738.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.683-11053A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897214 | ||||||
| chr4:17897215
|
T | C | 13 | a0001c0001t0010g0226a0001c0001t0040g0224a0001c0003t0001g0239others(10): Show | 13 | HG01175.hp2 HG01346.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.683-11054A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897215 | ||||||
| chr4:17897216
|
T | C | 16 | a0001c0003t0003g0215a0001c0003t0003g0216a0001c0003t0003g0234others(13): Show | 16 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-11055A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897216 | ||||||
| chr4:17897217
|
T | C | 18 | a0001c0003t0003g0214a0001c0003t0003g0240a0001c0003t0003g0244others(15): Show | 19 | HG00423.hp1 HG00639.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-11056A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897217 | ||||||
| chr4:17897218
|
T | C | 1 | a0001c0003t0003g0233 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.683-11057A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897218 | ||||||
| chr4:17897220
|
T | C | 3 | a0001c0001t0001g0132a0001c0001t0006g0120a0001c0001t0006g0121 | 3 | HG02895.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.683-11059A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897220 | ||||||
| chr4:17897221
|
T | C | 3 | a0001c0001t0016g0140a0002c0002t0002g0004a0022c0022t0016g0138 | 3 | HG02071.hp1 NA18951.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.683-11060A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897221 | ||||||
| chr4:17897224
|
T | C | 4 | a0001c0001t0005g0114a0002c0002t0014g0212a0004c0024t0013g0088others(1): Show | 4 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-11063A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897224 | ||||||
| chr4:17897225
|
T | C | 23 | a0002c0002t0005g0111a0002c0002t0005g0112a0002c0002t0005g0113others(20): Show | 23 | HG01081.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.683-11064A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897225 | ||||||
| chr4:17897226
|
T | C | 16 | a0001c0003t0003g0262a0001c0003t0003g0263a0002c0002t0002g0083others(13): Show | 16 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-11065A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897226 | ||||||
| chr4:17897227
|
T | C | 1 | a0004c0005t0031g0284 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.683-11066A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897227 | ||||||
| chr4:17897230
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0201a0002c0002t0002g0064others(1): Show | 4 | HG02622.hp2 HG03239.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-11069A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897230 | ||||||
| chr4:17897231
|
T | C | 16 | a0003c0004t0004g0094a0003c0004t0004g0096a0003c0004t0004g0097others(13): Show | 16 | HG00673.hp1 HG02602.hp2 HG03017.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-11070A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897231 | ||||||
| chr4:17897328
|
G | A | 39 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(36): Show | 39 | HG01081.hp2 HG01109.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.683-11167C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897328 | ||||||
| chr4:17897411
|
A | C | 2 | a0003c0004t0010g0100a0003c0004t0010g0102 | 2 | NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.683-11250T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897411 | ||||||
| chr4:17897423
|
T | C | 4 | a0002c0002t0002g0036a0002c0002t0002g0039a0002c0002t0002g0053others(1): Show | 4 | HG01071.hp2 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-11262A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897423 | ||||||
| chr4:17897555
|
T | C | 39 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(36): Show | 39 | HG01081.hp2 HG01109.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.683-11394A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897555 | ||||||
| chr4:17897589
|
A | T | 1 | a0003c0004t0004g0127 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.683-11428T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897589 | ||||||
| chr4:17897649
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.682+11445C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897649 | ||||||
| chr4:17897684
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.682+11410G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897684 | ||||||
| chr4:17897685
|
G | A | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.682+11409C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897685 | ||||||
| chr4:17897845
|
T | C | 1 | a0001c0001t0029g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.682+11249A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897845 | ||||||
| chr4:17897956
|
A | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.682+11138T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897956 | ||||||
| chr4:17897994
|
G | T | 1 | a0003c0004t0004g0119 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.682+11100C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17897994 | ||||||
| chr4:17898018
|
C | A | 4 | a0004c0024t0013g0088a0007c0008t0013g0217a0007c0008t0013g0218others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+11076G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17898018 | ||||||
| chr4:17898274
|
C | A | 1 | a0002c0002t0002g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.682+10820G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17898274 | ||||||
| chr4:17898652
|
G | GT | 22 | a0001c0001t0001g0068a0001c0001t0001g0148a0001c0001t0010g0226others(19): Show | 22 | HG01071.hp2 HG01081.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.682+10441dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17898652 | ||||||
| chr4:17898652
|
G | GTTTT | 6 | a0005c0006t0005g0231a0005c0006t0011g0222a0005c0006t0011g0223others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+10438_682+1044 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17898652 | ||||||
| chr4:17898652
|
GT | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0122others(135): Show | 140 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.682+10441delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17898652 | ||||||
| chr4:17898652
|
GTTT | G | 13 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(10): Show | 13 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.682+10439_682+1044 others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17898652 | ||||||
| chr4:17898883
|
G | A | 1 | a0002c0002t0002g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.682+10211C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17898883 | ||||||
| chr4:17899284
|
A | T | 1 | a0012c0012t0003g0002 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.682+9810T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17899284 | ||||||
| chr4:17899431
|
G | T | 43 | a0001c0001t0001g0154a0001c0003t0001g0239a0001c0003t0003g0214others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.682+9663C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17899431 | ||||||
| chr4:17899495
|
C | T | 5 | a0006c0007t0006g0250a0006c0007t0006g0272a0006c0007t0006g0274others(2): Show | 5 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+9599G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17899495 | ||||||
| chr4:17899639
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.682+9455T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17899639 | ||||||
| chr4:17899717
|
A | G | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.682+9377T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17899717 | ||||||
| chr4:17899729
|
T | C | 9 | a0002c0002t0002g0024a0002c0002t0002g0038a0002c0002t0002g0060others(6): Show | 9 | HG00642.hp1 HG01069.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.682+9365A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17899729 | ||||||
| chr4:17899745
|
A | G | 43 | a0001c0001t0001g0154a0001c0003t0001g0239a0001c0003t0003g0214others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.682+9349T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17899745 | ||||||
| chr4:17900056
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(203): Show | 208 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.682+9038G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900056 | ||||||
| chr4:17900247
|
C | T | 3 | a0001c0001t0001g0134a0001c0001t0001g0151a0001c0001t0001g0153 | 3 | NA18985.hp1 NA19010.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.682+8847G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900247 | ||||||
| chr4:17900484
|
C | T | 42 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(39): Show | 43 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.682+8610G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900484 | ||||||
| chr4:17900490
|
G | A | 10 | a0004c0024t0013g0088a0006c0007t0006g0250a0006c0007t0006g0272others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.682+8604C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900490 | ||||||
| chr4:17900519
|
A | G | 2 | a0001c0001t0002g0025a0002c0002t0002g0026 | 2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.682+8575T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900519 | ||||||
| chr4:17900592
|
T | C | 1 | a0001c0003t0022g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.682+8502A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900592 | ||||||
| chr4:17900668
|
C | A | 1 | a0003c0004t0004g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.682+8426G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900668 | ||||||
| chr4:17900741
|
C | T | 3 | a0006c0007t0006g0274a0006c0007t0006g0277a0006c0007t0006g0278 | 3 | HG02451.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.682+8353G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900741 | ||||||
| chr4:17900753
|
G | A | 26 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+8341C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900753 | ||||||
| chr4:17900849
|
A | G | 1 | a0002c0002t0037g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.682+8245T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900849 | ||||||
| chr4:17900954
|
T | C | 2 | a0003c0004t0010g0100a0003c0004t0010g0102 | 2 | NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.682+8140A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900954 | ||||||
| chr4:17900968
|
C | T | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.682+8126G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17900968 | ||||||
| chr4:17901000
|
TG | T | 70 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0001g0239others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.682+8093delC | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901000 | ||||||
| chr4:17901020
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.682+8074G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901020 | ||||||
| chr4:17901071
|
T | A | 1 | a0003c0004t0004g0107 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.682+8023A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901071 | ||||||
| chr4:17901297
|
C | A | 70 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0001g0239others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.682+7797G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901297 | ||||||
| chr4:17901378
|
A | G | 32 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(29): Show | 32 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.682+7716T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901378 | ||||||
| chr4:17901386
|
T | TA | 22 | a0001c0001t0001g0192a0003c0004t0002g0109a0003c0004t0004g0094others(19): Show | 22 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(19): Show |
intron_variant | MODIFIER | c.682+7707dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901386 | ||||||
| chr4:17901386
|
TA | T | 27 | a0001c0001t0006g0120a0001c0001t0006g0121a0004c0005t0004g0220others(24): Show | 27 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.682+7707delT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901386 | ||||||
| chr4:17901386
|
TAA | T | 42 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(39): Show | 43 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.682+7706_682+7707d others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901386 | ||||||
| chr4:17901702
|
T | C | 6 | a0006c0007t0006g0250a0006c0007t0006g0272a0006c0007t0006g0274others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+7392A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901702 | ||||||
| chr4:17901793
|
C | T | 16 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.682+7301G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17901793 | ||||||
| chr4:17902031
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(201): Show | 206 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.682+7063G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17902031 | ||||||
| chr4:17902054
|
G | T | 10 | a0004c0024t0013g0088a0006c0007t0006g0250a0006c0007t0006g0272others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.682+7040C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17902054 | ||||||
| chr4:17902128
|
C | CCAA | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.682+6963_682+6965d others(5): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17902128 | ||||||
| chr4:17902263
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.682+6831G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17902263 | ||||||
| chr4:17902379
|
C | T | 6 | a0006c0007t0006g0250a0006c0007t0006g0272a0006c0007t0006g0274others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+6715G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17902379 | ||||||
| chr4:17902432
|
G | GT | 20 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(17): Show | 20 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.682+6661dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17902432 | ||||||
| chr4:17902432
|
G | T | 2 | a0003c0004t0004g0104a0003c0004t0004g0105 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.682+6662C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17902432 | ||||||
| chr4:17902975
|
T | C | 2 | a0013c0013t0002g0073a0013c0013t0002g0074 | 2 | HG00735.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.682+6119A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17902975 | ||||||
| chr4:17903202
|
A | G | 1 | a0002c0002t0002g0029 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.682+5892T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17903202 | ||||||
| chr4:17903235
|
A | G | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.682+5859T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17903235 | ||||||
| chr4:17903283
|
T | G | 1 | a0002c0002t0002g0076 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.682+5811A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17903283 | ||||||
| chr4:17903578
|
T | A | 1 | a0002c0002t0005g0111 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.682+5516A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17903578 | ||||||
| chr4:17903837
|
G | T | 1 | a0012c0012t0003g0002 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.682+5257C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17903837 | ||||||
| chr4:17903887
|
A | C | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.682+5207T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17903887 | ||||||
| chr4:17903951
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0019g0133a0001c0001t0019g0204 | 3 | HG02717.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.682+5143G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17903951 | ||||||
| chr4:17903967
|
C | G | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.682+5127G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17903967 | ||||||
| chr4:17904003
|
CATA | C | 6 | a0006c0007t0006g0250a0006c0007t0006g0272a0006c0007t0006g0274others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+5088_682+5090d others(5): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904003 | ||||||
| chr4:17904042
|
C | T | 2 | a0001c0003t0003g0246a0001c0003t0003g0249 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.682+5052G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904042 | ||||||
| chr4:17904131
|
T | C | 2 | a0004c0005t0008g0286a0004c0005t0008g0288 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.682+4963A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904131 | ||||||
| chr4:17904137
|
T | C | 14 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(11): Show | 14 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+4957A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904137 | ||||||
| chr4:17904137
|
T | G | 1 | a0009c0009t0001g0178 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.682+4957A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904137 | ||||||
| chr4:17904302
|
G | A | 1 | a0018c0021t0004g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.682+4792C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904302 | ||||||
| chr4:17904329
|
A | G | 1 | a0003c0004t0004g0097 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.682+4765T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904329 | ||||||
| chr4:17904416
|
A | G | 2 | a0001c0001t0017g0198a0001c0001t0017g0199 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.682+4678T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904416 | ||||||
| chr4:17904495
|
A | G | 1 | a0002c0002t0002g0037 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.682+4599T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904495 | ||||||
| chr4:17904597
|
C | T | 2 | a0001c0003t0001g0239a0001c0003t0025g0264 | 2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.682+4497G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904597 | ||||||
| chr4:17904604
|
C | T | 2 | a0006c0007t0006g0250a0006c0007t0006g0272 | 2 | HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.682+4490G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904604 | ||||||
| chr4:17904629
|
G | C | 1 | a0001c0001t0029g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.682+4465C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904629 | ||||||
| chr4:17904655
|
T | A | 2 | a0001c0001t0002g0025a0002c0002t0002g0026 | 2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.682+4439A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904655 | ||||||
| chr4:17904812
|
CTTTA | C | 5 | a0001c0001t0017g0198a0001c0001t0017g0199a0007c0008t0013g0217others(2): Show | 5 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+4278_682+4281d others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17904812 | ||||||
| chr4:17905179
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.682+3915A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17905179 | ||||||
| chr4:17905435
|
C | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.682+3659G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17905435 | ||||||
| chr4:17905476
|
G | A | 14 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(11): Show | 14 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+3618C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17905476 | ||||||
| chr4:17905748
|
G | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.682+3346C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17905748 | ||||||
| chr4:17905751
|
A | C | 1 | a0002c0002t0012g0058 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.682+3343T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17905751 | ||||||
| chr4:17905959
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.682+3135A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17905959 | ||||||
| chr4:17906136
|
T | A | 2 | a0006c0007t0006g0250a0006c0007t0006g0272 | 2 | HG01358.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.682+2958A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906136 | ||||||
| chr4:17906356
|
C | T | 4 | a0001c0003t0003g0236a0001c0003t0003g0237a0001c0003t0003g0258others(1): Show | 4 | HG01243.hp2 HG02040.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+2738G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906356 | ||||||
| chr4:17906367
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(87): Show | 91 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.682+2727A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906367 | ||||||
| chr4:17906385
|
C | T | 14 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(11): Show | 14 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+2709G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906385 | ||||||
| chr4:17906455
|
G | A | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.682+2639C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906455 | ||||||
| chr4:17906456
|
A | G | 8 | a0004c0005t0008g0283a0004c0005t0008g0286a0004c0005t0008g0287others(5): Show | 8 | HG02145.hp1 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+2638T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906456 | ||||||
| chr4:17906486
|
CAAG | C | 13 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(10): Show | 13 | HG01081.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.682+2605_682+2607d others(5): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906486 | ||||||
| chr4:17906568
|
A | AG | 3 | a0002c0002t0014g0211a0002c0002t0014g0212a0002c0002t0014g0213 | 3 | HG01891.hp2 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.682+2525dupC | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906568 | ||||||
| chr4:17906620
|
G | A | 10 | a0004c0024t0013g0088a0006c0007t0006g0250a0006c0007t0006g0272others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.682+2474C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906620 | ||||||
| chr4:17906688
|
C | CT | 52 | a0001c0001t0001g0193a0001c0001t0001g0207a0001c0001t0041g0152others(49): Show | 53 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.682+2405dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906688 | ||||||
| chr4:17906688
|
C | CTT | 20 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0006g0121others(17): Show | 20 | HG01074.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.682+2404_682+2405d others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906688 | ||||||
| chr4:17906747
|
C | T | 10 | a0004c0024t0013g0088a0006c0007t0006g0250a0006c0007t0006g0272others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.682+2347G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906747 | ||||||
| chr4:17906750
|
G | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.682+2344C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906750 | ||||||
| chr4:17906777
|
C | A | 10 | a0004c0024t0013g0088a0006c0007t0006g0250a0006c0007t0006g0272others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.682+2317G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906777 | ||||||
| chr4:17906779
|
C | T | 7 | a0001c0001t0001g0059a0001c0001t0001g0145a0001c0001t0001g0155others(4): Show | 7 | NA18955.hp1 NA18956.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+2315G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906779 | ||||||
| chr4:17906790
|
A | G | 71 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0006g0121others(68): Show | 72 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.682+2304T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906790 | ||||||
| chr4:17906841
|
C | T | 26 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+2253G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906841 | ||||||
| chr4:17906844
|
G | A | 26 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+2250C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906844 | ||||||
| chr4:17906910
|
T | C | 26 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+2184A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906910 | ||||||
| chr4:17906977
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.682+2117G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17906977 | ||||||
| chr4:17907164
|
C | A | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.682+1930G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907164 | ||||||
| chr4:17907216
|
T | C | 1 | a0012c0012t0003g0002 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.682+1878A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907216 | ||||||
| chr4:17907310
|
T | C | 3 | a0001c0003t0003g0238a0001c0003t0003g0251a0001c0003t0003g0253 | 3 | HG00639.hp1 HG01192.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.682+1784A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907310 | ||||||
| chr4:17907655
|
A | AT | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.682+1438dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907655 | ||||||
| chr4:17907667
|
C | T | 26 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(23): Show | 26 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+1427G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907667 | ||||||
| chr4:17907705
|
A | AC | 9 | a0006c0007t0006g0250a0006c0007t0006g0272a0006c0007t0006g0274others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.682+1388dupG | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907705 | ||||||
| chr4:17907716
|
G | A | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.682+1378C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907716 | ||||||
| chr4:17907786
|
T | C | 3 | a0002c0002t0005g0116a0002c0002t0005g0117a0002c0026t0005g0115 | 3 | HG01081.hp2 HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.682+1308A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907786 | ||||||
| chr4:17907842
|
T | G | 1 | a0001c0003t0001g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.682+1252A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907842 | ||||||
| chr4:17907863
|
C | T | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.682+1231G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17907863 | ||||||
| chr4:17908062
|
C | T | 3 | a0002c0002t0005g0116a0002c0002t0005g0117a0002c0026t0005g0115 | 3 | HG01081.hp2 HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.682+1032G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908062 | ||||||
| chr4:17908091
|
G | T | 44 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0001g0239others(41): Show | 45 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.682+1003C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908091 | ||||||
| chr4:17908102
|
G | A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.682+992C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908102 | ||||||
| chr4:17908220
|
TG | T | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.682+873delC | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908220 | ||||||
| chr4:17908249
|
C | G | 1 | a0001c0003t0003g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.682+845G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908249 | ||||||
| chr4:17908337
|
A | C | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.682+757T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908337 | ||||||
| chr4:17908502
|
G | C | 1 | a0001c0001t0012g0062 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.682+592C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908502 | ||||||
| chr4:17908518
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.682+576G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908518 | ||||||
| chr4:17908609
|
T | C | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.682+485A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908609 | ||||||
| chr4:17908613
|
C | A | 69 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0001g0239others(66): Show | 70 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.682+481G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17908613 | ||||||
| chr4:17909070
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.682+24A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 5/7 | chr4 | 17909070 | ||||||
| chr4:17909600
|
A | G | 1 | a0001c0001t0017g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.431-255T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17909600 | ||||||
| chr4:17909621
|
C | T | 2 | a0002c0002t0005g0209a0002c0002t0005g0210 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.431-276G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17909621 | ||||||
| chr4:17909827
|
A | T | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-482T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17909827 | ||||||
| chr4:17909862
|
T | A | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-517A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17909862 | ||||||
| chr4:17909994
|
A | G | 2 | a0001c0003t0003g0215a0001c0003t0003g0245 | 2 | NA19005.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.431-649T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17909994 | ||||||
| chr4:17910046
|
A | T | 1 | a0002c0002t0005g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.431-701T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910046 | ||||||
| chr4:17910168
|
A | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-823T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910168 | ||||||
| chr4:17910194
|
G | C | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.431-849C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910194 | ||||||
| chr4:17910217
|
G | C | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-872C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910217 | ||||||
| chr4:17910242
|
T | C | 2 | a0001c0001t0016g0140a0022c0022t0016g0138 | 2 | HG02071.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.431-897A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910242 | ||||||
| chr4:17910282
|
C | T | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-937G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910282 | ||||||
| chr4:17910498
|
C | T | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.431-1153G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910498 | ||||||
| chr4:17910601
|
T | C | 1 | a0001c0001t0007g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.431-1256A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910601 | ||||||
| chr4:17910609
|
G | C | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-1264C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910609 | ||||||
| chr4:17910647
|
G | A | 10 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.431-1302C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910647 | ||||||
| chr4:17910768
|
T | C | 3 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224 | 3 | HG02896.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.431-1423A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910768 | ||||||
| chr4:17910859
|
A | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-1514T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910859 | ||||||
| chr4:17910883
|
G | T | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.431-1538C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910883 | ||||||
| chr4:17910916
|
T | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-1571A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910916 | ||||||
| chr4:17910985
|
G | T | 11 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-1640C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17910985 | ||||||
| chr4:17911097
|
A | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431-1752T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17911097 | ||||||
| chr4:17911278
|
CAAATGGC others(8): Show |
C | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.431-1948_431-1934d others(17): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17911278 | ||||||
| chr4:17911326
|
A | G | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.431-1981T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17911326 | ||||||
| chr4:17911328
|
C | T | 16 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.431-1983G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17911328 | ||||||
| chr4:17911775
|
C | T | 4 | a0001c0003t0003g0214a0001c0003t0003g0252a0001c0003t0003g0255others(1): Show | 4 | NA18946.hp2 NA19002.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-2430G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17911775 | ||||||
| chr4:17911776
|
G | A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.431-2431C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17911776 | ||||||
| chr4:17911791
|
G | A | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.431-2446C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17911791 | ||||||
| chr4:17911853
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0207 | 3 | HG01433.hp2 HG01928.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.431-2508G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17911853 | ||||||
| chr4:17911877
|
C | T | 1 | a0007c0008t0013g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.431-2532G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17911877 | ||||||
| chr4:17912038
|
G | C | 1 | a0001c0001t0006g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.431-2693C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912038 | ||||||
| chr4:17912240
|
CATT | C | 6 | a0001c0001t0001g0196a0001c0001t0001g0201a0001c0001t0017g0198others(3): Show | 6 | HG02622.hp2 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-2898_431-2896d others(5): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912240 | ||||||
| chr4:17912256
|
A | G | 44 | a0001c0001t0001g0154a0001c0003t0001g0239a0001c0003t0003g0214others(41): Show | 45 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.431-2911T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912256 | ||||||
| chr4:17912263
|
C | A | 3 | a0001c0001t0001g0132a0001c0001t0019g0133a0001c0001t0019g0204 | 3 | HG02717.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.431-2918G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912263 | ||||||
| chr4:17912364
|
C | G | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.431-3019G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912364 | ||||||
| chr4:17912490
|
G | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-3145C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912490 | ||||||
| chr4:17912630
|
T | C | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-3285A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912630 | ||||||
| chr4:17912634
|
G | A | 5 | a0001c0003t0003g0233a0001c0003t0003g0234a0001c0003t0003g0270others(2): Show | 5 | HG00735.hp1 HG00738.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.431-3289C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912634 | ||||||
| chr4:17912664
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.431-3319G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912664 | ||||||
| chr4:17912727
|
C | A | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-3382G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912727 | ||||||
| chr4:17912945
|
C | T | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-3600G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17912945 | ||||||
| chr4:17913065
|
A | G | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-3720T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17913065 | ||||||
| chr4:17913151
|
A | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-3806T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17913151 | ||||||
| chr4:17913389
|
G | C | 1 | a0020c0023t0002g0005 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.431-4044C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17913389 | ||||||
| chr4:17913424
|
T | G | 1 | a0001c0001t0001g0059 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.431-4079A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17913424 | ||||||
| chr4:17913438
|
C | A | 2 | a0004c0005t0008g0280a0004c0005t0008g0281 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.431-4093G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17913438 | ||||||
| chr4:17913819
|
C | T | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-4474G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17913819 | ||||||
| chr4:17913837
|
G | T | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-4492C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17913837 | ||||||
| chr4:17913862
|
C | T | 1 | a0003c0004t0004g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.431-4517G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17913862 | ||||||
| chr4:17913959
|
C | T | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-4614G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17913959 | ||||||
| chr4:17914069
|
A | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-4724T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914069 | ||||||
| chr4:17914088
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.431-4743A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914088 | ||||||
| chr4:17914185
|
T | C | 1 | a0002c0002t0002g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.431-4840A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914185 | ||||||
| chr4:17914231
|
C | A | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-4886G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914231 | ||||||
| chr4:17914302
|
T | C | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-4957A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914302 | ||||||
| chr4:17914418
|
G | T | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431-5073C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914418 | ||||||
| chr4:17914464
|
T | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-5119A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914464 | ||||||
| chr4:17914508
|
A | G | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.431-5163T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914508 | ||||||
| chr4:17914787
|
A | C | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.431-5442T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914787 | ||||||
| chr4:17914880
|
T | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.431-5535A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914880 | ||||||
| chr4:17914989
|
T | C | 1 | a0002c0002t0037g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.431-5644A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17914989 | ||||||
| chr4:17915013
|
T | G | 2 | a0001c0001t0001g0191a0003c0004t0004g0127 | 2 | NA19078.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.431-5668A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17915013 | ||||||
| chr4:17915045
|
T | C | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.431-5700A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17915045 | ||||||
| chr4:17915366
|
A | G | 1 | a0002c0002t0002g0031 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.431-6021T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17915366 | ||||||
| chr4:17915567
|
A | G | 46 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0006g0121others(43): Show | 47 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.431-6222T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17915567 | ||||||
| chr4:17915689
|
C | T | 1 | a0001c0001t0029g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.431-6344G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17915689 | ||||||
| chr4:17915713
|
A | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431-6368T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17915713 | ||||||
| chr4:17915833
|
A | G | 1 | a0002c0002t0035g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.431-6488T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17915833 | ||||||
| chr4:17915903
|
T | C | 9 | a0004c0024t0013g0088a0006c0007t0006g0272a0006c0007t0006g0274others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-6558A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17915903 | ||||||
| chr4:17915970
|
G | A | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.431-6625C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17915970 | ||||||
| chr4:17916158
|
A | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(189): Show | 194 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.431-6813T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916158 | ||||||
| chr4:17916175
|
G | A | 1 | a0022c0022t0016g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.431-6830C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916175 | ||||||
| chr4:17916195
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(189): Show | 194 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.431-6850C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916195 | ||||||
| chr4:17916346
|
A | G | 1 | a0002c0002t0002g0087 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.431-7001T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916346 | ||||||
| chr4:17916398
|
A | T | 1 | a0001c0001t0001g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.431-7053T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916398 | ||||||
| chr4:17916447
|
C | T | 19 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(16): Show | 19 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.431-7102G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916447 | ||||||
| chr4:17916643
|
C | CT | 59 | a0001c0001t0001g0136a0001c0001t0001g0145a0001c0001t0001g0146others(56): Show | 60 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.431-7299dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916643 | ||||||
| chr4:17916643
|
C | CTT | 6 | a0001c0003t0001g0239a0001c0003t0003g0236a0001c0003t0003g0238others(3): Show | 6 | HG00673.hp2 HG01175.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-7300_431-7299d others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916643 | ||||||
| chr4:17916643
|
CT | C | 9 | a0001c0001t0001g0089a0001c0001t0001g0124a0001c0001t0001g0158others(6): Show | 9 | HG01891.hp1 HG01943.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-7299delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916643 | ||||||
| chr4:17916643
|
CTT | C | 21 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.431-7300_431-7299d others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916643 | ||||||
| chr4:17916705
|
C | T | 1 | a0006c0007t0006g0272 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.431-7360G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916705 | ||||||
| chr4:17916756
|
T | C | 16 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.431-7411A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916756 | ||||||
| chr4:17916765
|
C | T | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-7420G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916765 | ||||||
| chr4:17916770
|
G | A | 46 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0006g0121others(43): Show | 47 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.431-7425C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916770 | ||||||
| chr4:17916963
|
A | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-7618T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17916963 | ||||||
| chr4:17917077
|
C | A | 45 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0001g0239others(42): Show | 46 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.431-7732G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917077 | ||||||
| chr4:17917077
|
C | T | 9 | a0004c0024t0013g0088a0006c0007t0006g0272a0006c0007t0006g0274others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-7732G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917077 | ||||||
| chr4:17917213
|
T | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(118): Show | 122 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.431-7868A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917213 | ||||||
| chr4:17917239
|
A | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-7894T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917239 | ||||||
| chr4:17917312
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.431-7967G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917312 | ||||||
| chr4:17917366
|
T | C | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-8021A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917366 | ||||||
| chr4:17917440
|
G | A | 2 | a0004c0005t0008g0286a0004c0005t0008g0288 | 2 | HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.431-8095C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917440 | ||||||
| chr4:17917443
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(155): Show | 160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.431-8098G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917443 | ||||||
| chr4:17917529
|
G | A | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-8184C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917529 | ||||||
| chr4:17917940
|
A | AAAAAC | 8 | a0001c0001t0002g0065a0001c0003t0003g0247a0002c0002t0002g0041others(5): Show | 8 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.431-8600_431-8596d others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917940 | ||||||
| chr4:17917940
|
A | AAAAACAA others(3): Show |
10 | a0004c0005t0008g0280a0004c0005t0008g0283a0004c0005t0008g0286others(7): Show | 10 | HG02145.hp1 HG02615.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.431-8605_431-8596d others(12): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917940 | ||||||
| chr4:17917940
|
A | AAAAACAA others(8): Show |
2 | a0004c0005t0008g0281a0004c0005t0008g0282 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.431-8610_431-8596d others(17): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917940 | ||||||
| chr4:17917940
|
A | AAAAACAA others(13): Show |
1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431-8615_431-8596d others(22): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917940 | ||||||
| chr4:17917940
|
AAAAAC | A | 25 | a0001c0001t0001g0147a0001c0001t0005g0114a0001c0001t0010g0226others(22): Show | 25 | HG01081.hp2 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.431-8600_431-8596d others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917940 | ||||||
| chr4:17917940
|
AAAAACAA others(3): Show |
A | 1 | a0002c0002t0002g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.431-8605_431-8596d others(12): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917940 | ||||||
| chr4:17917986
|
C | A | 1 | a0002c0002t0002g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.431-8641G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17917986 | ||||||
| chr4:17918103
|
T | C | 2 | a0002c0002t0020g0275a0002c0002t0020g0276 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.431-8758A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17918103 | ||||||
| chr4:17918188
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(188): Show | 193 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(190): Show |
intron_variant | MODIFIER | c.431-8843C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17918188 | ||||||
| chr4:17918264
|
C | T | 8 | a0001c0001t0001g0059a0001c0001t0001g0145a0001c0001t0001g0155others(5): Show | 8 | NA18955.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.431-8919G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17918264 | ||||||
| chr4:17918466
|
C | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-9121G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17918466 | ||||||
| chr4:17918508
|
A | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-9163T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17918508 | ||||||
| chr4:17918673
|
A | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-9328T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17918673 | ||||||
| chr4:17919064
|
G | A | 2 | a0001c0001t0023g0007a0003c0004t0004g0107 | 2 | HG03017.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.431-9719C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17919064 | ||||||
| chr4:17919267
|
C | T | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431-9922G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17919267 | ||||||
| chr4:17919342
|
C | G | 1 | a0013c0013t0002g0074 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.431-9997G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17919342 | ||||||
| chr4:17919624
|
T | C | 1 | a0004c0005t0008g0287 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.431-10279A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17919624 | ||||||
| chr4:17920042
|
C | T | 4 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0229others(1): Show | 4 | HG02145.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-10697G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17920042 | ||||||
| chr4:17920268
|
G | A | 1 | a0002c0002t0002g0056 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.431-10923C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17920268 | ||||||
| chr4:17920381
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.431-11036A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17920381 | ||||||
| chr4:17920690
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0019g0133a0001c0001t0019g0204 | 3 | HG02717.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.431-11345G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17920690 | ||||||
| chr4:17920739
|
T | A | 2 | a0001c0003t0003g0246a0001c0003t0003g0249 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.431-11394A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17920739 | ||||||
| chr4:17920741
|
C | A | 3 | a0006c0007t0006g0274a0006c0007t0006g0277a0006c0007t0006g0278 | 3 | HG02451.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.431-11396G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17920741 | ||||||
| chr4:17920867
|
T | C | 4 | a0006c0007t0006g0272a0006c0007t0006g0274a0006c0007t0006g0277others(1): Show | 4 | HG01358.hp2 HG02451.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-11522A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17920867 | ||||||
| chr4:17921008
|
G | C | 1 | a0002c0002t0002g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.431-11663C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921008 | ||||||
| chr4:17921045
|
G | A | 20 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(17): Show | 20 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.431-11700C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921045 | ||||||
| chr4:17921102
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.431-11757G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921102 | ||||||
| chr4:17921148
|
C | T | 11 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-11803G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921148 | ||||||
| chr4:17921190
|
A | AT | 54 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0006g0121others(51): Show | 55 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.431-11846dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921190 | ||||||
| chr4:17921243
|
A | G | 71 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0006g0121others(68): Show | 72 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.431-11898T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921243 | ||||||
| chr4:17921666
|
T | C | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.431-12321A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921666 | ||||||
| chr4:17921691
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(83): Show | 87 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.431-12346G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921691 | ||||||
| chr4:17921721
|
G | A | 1 | a0001c0003t0003g0271 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.431-12376C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921721 | ||||||
| chr4:17921833
|
A | G | 287 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(284): Show | 289 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(286): Show |
intron_variant | MODIFIER | c.431-12488T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921833 | ||||||
| chr4:17921954
|
C | G | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.431-12609G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17921954 | ||||||
| chr4:17922018
|
G | A | 1 | a0001c0003t0003g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.431-12673C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922018 | ||||||
| chr4:17922310
|
T | C | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-12965A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922310 | ||||||
| chr4:17922402
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431-13057A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922402 | ||||||
| chr4:17922475
|
C | T | 10 | a0002c0002t0002g0076a0004c0024t0013g0088a0006c0007t0006g0272others(7): Show | 10 | HG01109.hp2 HG01123.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.431-13130G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922475 | ||||||
| chr4:17922502
|
G | C | 3 | a0002c0002t0002g0030a0002c0002t0002g0032a0002c0002t0002g0033 | 3 | NA18943.hp1 NA18949.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.431-13157C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922502 | ||||||
| chr4:17922534
|
A | T | 1 | a0001c0003t0003g0263 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.431-13189T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922534 | ||||||
| chr4:17922620
|
G | A | 1 | a0001c0001t0006g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.431-13275C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922620 | ||||||
| chr4:17922745
|
T | C | 1 | a0003c0004t0004g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.431-13400A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922745 | ||||||
| chr4:17922773
|
T | C | 4 | a0006c0007t0006g0272a0006c0007t0006g0274a0006c0007t0006g0277others(1): Show | 4 | HG01358.hp2 HG02451.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-13428A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922773 | ||||||
| chr4:17922803
|
C | A | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-13458G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922803 | ||||||
| chr4:17922835
|
A | G | 1 | a0001c0001t0006g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.431-13490T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17922835 | ||||||
| chr4:17923111
|
T | C | 71 | a0001c0001t0001g0206a0001c0001t0006g0120a0001c0001t0006g0121others(68): Show | 72 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.431-13766A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923111 | ||||||
| chr4:17923177
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.431-13832A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923177 | ||||||
| chr4:17923267
|
G | C | 1 | a0001c0003t0003g0271 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.431-13922C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923267 | ||||||
| chr4:17923344
|
T | C | 1 | a0001c0003t0003g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.431-13999A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923344 | ||||||
| chr4:17923421
|
G | A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431-14076C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923421 | ||||||
| chr4:17923441
|
T | C | 1 | a0001c0003t0003g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.431-14096A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923441 | ||||||
| chr4:17923739
|
AG | A | 4 | a0004c0024t0013g0088a0007c0008t0013g0217a0007c0008t0013g0218others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-14395delC | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923739 | ||||||
| chr4:17923845
|
G | C | 9 | a0004c0024t0013g0088a0006c0007t0006g0272a0006c0007t0006g0274others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-14500C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923845 | ||||||
| chr4:17923875
|
G | A | 2 | a0002c0002t0002g0050a0002c0002t0002g0165 | 2 | NA19009.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.431-14530C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923875 | ||||||
| chr4:17923912
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.431-14567G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923912 | ||||||
| chr4:17923927
|
G | A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.431-14582C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923927 | ||||||
| chr4:17923995
|
C | T | 45 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0001g0239others(42): Show | 46 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.431-14650G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17923995 | ||||||
| chr4:17924152
|
G | A | 3 | a0001c0003t0003g0238a0001c0003t0003g0251a0001c0003t0003g0253 | 3 | HG00639.hp1 HG01192.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.431-14807C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17924152 | ||||||
| chr4:17924175
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(166): Show | 171 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.431-14830A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17924175 | ||||||
| chr4:17924446
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0146 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.431-15101C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17924446 | ||||||
| chr4:17924484
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.431-15139C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17924484 | ||||||
| chr4:17924609
|
C | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-15264G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17924609 | ||||||
| chr4:17924791
|
G | A | 1 | a0001c0003t0022g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.431-15446C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17924791 | ||||||
| chr4:17924829
|
A | G | 1 | a0004c0005t0008g0289 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.431-15484T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17924829 | ||||||
| chr4:17924860
|
C | T | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.431-15515G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17924860 | ||||||
| chr4:17924914
|
G | C | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.431-15569C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17924914 | ||||||
| chr4:17925238
|
T | A | 1 | a0001c0001t0001g0188 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.431-15893A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925238 | ||||||
| chr4:17925280
|
T | C | 1 | a0003c0004t0004g0107 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.431-15935A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925280 | ||||||
| chr4:17925427
|
G | A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.431-16082C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925427 | ||||||
| chr4:17925477
|
C | T | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.431-16132G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925477 | ||||||
| chr4:17925699
|
G | A | 1 | a0001c0003t0003g0254 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.431-16354C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925699 | ||||||
| chr4:17925715
|
C | T | 4 | a0002c0002t0005g0116a0002c0002t0005g0117a0002c0002t0020g0275others(1): Show | 4 | HG01081.hp2 HG02257.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-16370G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925715 | ||||||
| chr4:17925763
|
C | T | 6 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0222others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-16418G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925763 | ||||||
| chr4:17925786
|
G | A | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.431-16441C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925786 | ||||||
| chr4:17925797
|
G | T | 5 | a0006c0007t0006g0272a0006c0007t0006g0274a0006c0007t0006g0277others(2): Show | 5 | HG01358.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-16452C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925797 | ||||||
| chr4:17925878
|
C | CA | 43 | a0001c0001t0002g0065a0001c0001t0005g0114a0001c0001t0012g0062others(40): Show | 43 | HG00438.hp2 HG01081.hp2 HG01433.hp1 others(40): Show |
intron_variant | MODIFIER | c.431-16534dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925878 | ||||||
| chr4:17925878
|
C | CAA | 6 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224others(3): Show | 6 | HG02257.hp1 HG02896.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-16535_431-1653 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925878 | ||||||
| chr4:17925878
|
CA | C | 41 | a0001c0001t0001g0154a0001c0001t0006g0120a0001c0001t0007g0016others(38): Show | 42 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.431-16534delT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925878 | ||||||
| chr4:17925878
|
CAAAAA | C | 18 | a0004c0005t0008g0282a0004c0005t0008g0283a0004c0005t0008g0286others(15): Show | 18 | HG01358.hp2 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.431-16538_431-1653 others(9): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925878 | ||||||
| chr4:17925878
|
CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0001g0090a0001c0001t0001g0128a0001c0001t0001g0172others(4): Show | 7 | HG01109.hp2 HG01243.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-16544_431-1653 others(15): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925878 | ||||||
| chr4:17925878
|
CAAAAAAA others(5): Show |
C | 84 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(81): Show | 85 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.431-16545_431-1653 others(16): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925878 | ||||||
| chr4:17925909
|
C | G | 9 | a0004c0024t0013g0088a0006c0007t0006g0272a0006c0007t0006g0274others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-16564G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925909 | ||||||
| chr4:17925972
|
C | T | 15 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(12): Show | 15 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.431-16627G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17925972 | ||||||
| chr4:17926002
|
C | T | 1 | a0002c0002t0001g0085 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.431-16657G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17926002 | ||||||
| chr4:17926193
|
C | T | 3 | a0001c0003t0003g0233a0001c0003t0003g0234a0001c0003t0003g0270 | 3 | HG00738.hp2 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.431-16848G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17926193 | ||||||
| chr4:17926197
|
T | C | 20 | a0001c0001t0001g0169a0003c0004t0002g0109a0003c0004t0004g0094others(17): Show | 20 | HG00673.hp1 HG02602.hp2 HG03017.hp1 others(17): Show |
intron_variant | MODIFIER | c.431-16852A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17926197 | ||||||
| chr4:17926298
|
C | T | 6 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0222others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-16953G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17926298 | ||||||
| chr4:17926305
|
C | CAA | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-16962_431-1696 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17926305 | ||||||
| chr4:17926438
|
G | C | 3 | a0006c0007t0006g0250a0010c0014t0015g0248a0010c0014t0015g0259 | 3 | HG02683.hp2 HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.431-17093C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17926438 | ||||||
| chr4:17926478
|
A | G | 11 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(8): Show | 11 | HG02145.hp2 HG02572.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-17133T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17926478 | ||||||
| chr4:17926486
|
C | T | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431-17141G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17926486 | ||||||
| chr4:17926981
|
C | T | 1 | a0005c0006t0011g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.431-17636G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17926981 | ||||||
| chr4:17927106
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-17761A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17927106 | ||||||
| chr4:17927551
|
T | C | 1 | a0002c0002t0002g0078 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.431-18206A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17927551 | ||||||
| chr4:17927662
|
A | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-18317T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17927662 | ||||||
| chr4:17927739
|
G | A | 1 | a0003c0004t0004g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.431-18394C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17927739 | ||||||
| chr4:17927759
|
C | G | 1 | a0001c0025t0026g0205 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.431-18414G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17927759 | ||||||
| chr4:17927815
|
G | A | 1 | a0002c0002t0002g0060 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.431-18470C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17927815 | ||||||
| chr4:17927872
|
A | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-18527T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17927872 | ||||||
| chr4:17927929
|
T | TA | 9 | a0004c0024t0013g0088a0006c0007t0006g0272a0006c0007t0006g0274others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-18585dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17927929 | ||||||
| chr4:17928124
|
T | C | 45 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0003t0001g0239others(42): Show | 46 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.431-18779A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17928124 | ||||||
| chr4:17928133
|
A | G | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.431-18788T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17928133 | ||||||
| chr4:17928273
|
G | C | 3 | a0006c0007t0006g0274a0006c0007t0006g0277a0006c0007t0006g0278 | 3 | HG02451.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.431-18928C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17928273 | ||||||
| chr4:17928331
|
T | G | 25 | a0004c0005t0004g0220a0004c0005t0008g0280a0004c0005t0008g0281others(22): Show | 25 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-18986A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17928331 | ||||||
| chr4:17928928
|
GAACT | G | 4 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0229others(1): Show | 4 | HG02145.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-19587_431-1958 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17928928 | ||||||
| chr4:17928938
|
T | C | 1 | a0001c0003t0022g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.431-19593A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17928938 | ||||||
| chr4:17928986
|
T | C | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.431-19641A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17928986 | ||||||
| chr4:17929050
|
C | T | 1 | a0001c0001t0009g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.431-19705G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17929050 | ||||||
| chr4:17929068
|
A | G | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.431-19723T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17929068 | ||||||
| chr4:17929195
|
G | A | 1 | a0003c0004t0004g0110 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.431-19850C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17929195 | ||||||
| chr4:17929534
|
C | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-20189G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17929534 | ||||||
| chr4:17929695
|
T | C | 68 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(65): Show | 69 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.431-20350A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17929695 | ||||||
| chr4:17929900
|
C | A | 2 | a0002c0002t0020g0275a0002c0002t0020g0276 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.431-20555G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17929900 | ||||||
| chr4:17930105
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.431-20760G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930105 | ||||||
| chr4:17930113
|
G | A | 2 | a0014c0011t0004g0092a0014c0011t0004g0093 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.431-20768C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930113 | ||||||
| chr4:17930647
|
C | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-21302G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930647 | ||||||
| chr4:17930692
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-21347A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930692 | ||||||
| chr4:17930696
|
C | T | 68 | a0001c0001t0001g0201a0001c0001t0006g0120a0001c0001t0006g0121others(65): Show | 69 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.431-21351G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930696 | ||||||
| chr4:17930714
|
C | T | 1 | a0004c0005t0008g0286 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.431-21369G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930714 | ||||||
| chr4:17930790
|
C | T | 1 | a0001c0001t0009g0166 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.431-21445G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930790 | ||||||
| chr4:17930932
|
A | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.431-21587T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930932 | ||||||
| chr4:17930976
|
C | A | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-21631G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930976 | ||||||
| chr4:17930995
|
T | C | 1 | a0020c0023t0002g0005 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.431-21650A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17930995 | ||||||
| chr4:17931363
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.431-22018G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17931363 | ||||||
| chr4:17931778
|
T | A | 27 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(24): Show | 27 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.431-22433A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17931778 | ||||||
| chr4:17931848
|
C | A | 1 | a0005c0006t0011g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.431-22503G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17931848 | ||||||
| chr4:17931952
|
G | A | 1 | a0005c0006t0011g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.431-22607C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17931952 | ||||||
| chr4:17932016
|
C | T | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.431-22671G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932016 | ||||||
| chr4:17932047
|
G | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(154): Show | 159 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.431-22702C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932047 | ||||||
| chr4:17932074
|
T | G | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.431-22729A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932074 | ||||||
| chr4:17932087
|
G | C | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.431-22742C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932087 | ||||||
| chr4:17932187
|
C | G | 79 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(76): Show | 80 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.431-22842G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932187 | ||||||
| chr4:17932639
|
G | C | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.431-23294C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932639 | ||||||
| chr4:17932657
|
G | A | 1 | a0001c0003t0022g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.431-23312C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932657 | ||||||
| chr4:17932665
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.431-23320C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932665 | ||||||
| chr4:17932740
|
G | A | 5 | a0006c0007t0006g0272a0006c0007t0006g0274a0006c0007t0006g0277others(2): Show | 5 | HG01358.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-23395C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932740 | ||||||
| chr4:17932771
|
A | T | 79 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(76): Show | 80 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.431-23426T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932771 | ||||||
| chr4:17932838
|
T | C | 79 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(76): Show | 80 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.431-23493A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932838 | ||||||
| chr4:17932862
|
G | C | 1 | a0002c0002t0002g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.431-23517C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17932862 | ||||||
| chr4:17933119
|
A | T | 25 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(22): Show | 25 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-23774T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933119 | ||||||
| chr4:17933121
|
C | A | 25 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(22): Show | 25 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-23776G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933121 | ||||||
| chr4:17933123
|
T | A | 25 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(22): Show | 25 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-23778A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933123 | ||||||
| chr4:17933124
|
ACTTT | A | 25 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(22): Show | 25 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-23783_431-2378 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933124 | ||||||
| chr4:17933422
|
C | G | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.431-24077G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933422 | ||||||
| chr4:17933460
|
T | C | 9 | a0004c0024t0013g0088a0006c0007t0006g0272a0006c0007t0006g0274others(6): Show | 9 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.431-24115A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933460 | ||||||
| chr4:17933536
|
C | T | 11 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-24191G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933536 | ||||||
| chr4:17933620
|
A | C | 11 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.431-24275T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933620 | ||||||
| chr4:17933697
|
A | G | 8 | a0001c0001t0001g0059a0001c0001t0001g0145a0001c0001t0001g0155others(5): Show | 8 | NA18955.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.431-24352T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933697 | ||||||
| chr4:17933954
|
G | GT | 4 | a0006c0007t0006g0272a0006c0007t0006g0274a0006c0007t0006g0277others(1): Show | 4 | HG01358.hp2 HG02451.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.431-24610dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933954 | ||||||
| chr4:17933996
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.431-24651A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17933996 | ||||||
| chr4:17934013
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.431-24668A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17934013 | ||||||
| chr4:17934198
|
T | G | 3 | a0001c0001t0001g0132a0001c0001t0019g0133a0001c0001t0019g0204 | 3 | HG02717.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.431-24853A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17934198 | ||||||
| chr4:17934497
|
A | G | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.431-25152T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17934497 | ||||||
| chr4:17934570
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.431-25225A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17934570 | ||||||
| chr4:17934820
|
C | T | 76 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(73): Show | 77 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.431-25475G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17934820 | ||||||
| chr4:17935011
|
T | C | 76 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(73): Show | 77 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.431-25666A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935011 | ||||||
| chr4:17935057
|
A | G | 1 | a0002c0002t0002g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.431-25712T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935057 | ||||||
| chr4:17935137
|
C | G | 2 | a0001c0001t0016g0140a0022c0022t0016g0138 | 2 | HG02071.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.431-25792G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935137 | ||||||
| chr4:17935171
|
G | A | 6 | a0004c0024t0013g0088a0006c0007t0006g0272a0006c0007t0006g0274others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-25826C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935171 | ||||||
| chr4:17935192
|
C | A | 1 | a0001c0001t0002g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.431-25847G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935192 | ||||||
| chr4:17935305
|
TTAGA | T | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.431-25964_431-2596 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935305 | ||||||
| chr4:17935330
|
A | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.431-25985T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935330 | ||||||
| chr4:17935438
|
T | A | 8 | a0001c0001t0001g0059a0001c0001t0001g0145a0001c0001t0001g0155others(5): Show | 8 | NA18955.hp1 NA18956.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.431-26093A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935438 | ||||||
| chr4:17935476
|
G | A | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.431-26131C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935476 | ||||||
| chr4:17935681
|
G | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(275): Show | 280 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(277): Show |
intron_variant | MODIFIER | c.430+26222C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935681 | ||||||
| chr4:17935738
|
C | T | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+26165G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17935738 | ||||||
| chr4:17936005
|
A | G | 1 | a0003c0004t0004g0101 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.430+25898T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936005 | ||||||
| chr4:17936059
|
T | C | 1 | a0007c0008t0013g0218 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.430+25844A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936059 | ||||||
| chr4:17936278
|
C | T | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430+25625G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936278 | ||||||
| chr4:17936360
|
G | GA | 7 | a0001c0001t0001g0149a0001c0001t0001g0167a0001c0003t0003g0263others(4): Show | 7 | HG02622.hp1 HG02970.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+25542dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936360 | ||||||
| chr4:17936360
|
G | GAA | 72 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(69): Show | 73 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.430+25541_430+2554 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936360 | ||||||
| chr4:17936473
|
T | C | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.430+25430A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936473 | ||||||
| chr4:17936515
|
T | C | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.430+25388A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936515 | ||||||
| chr4:17936671
|
T | C | 27 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(24): Show | 27 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.430+25232A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936671 | ||||||
| chr4:17936769
|
C | T | 1 | a0002c0002t0005g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.430+25134G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936769 | ||||||
| chr4:17936782
|
A | AT | 3 | a0009c0009t0001g0178a0009c0009t0001g0186a0009c0009t0001g0187 | 3 | HG02056.hp2 NA18948.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.430+25120dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936782 | ||||||
| chr4:17936794
|
A | C | 8 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0181others(5): Show | 8 | HG00642.hp2 HG01346.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+25109T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936794 | ||||||
| chr4:17936868
|
C | A | 2 | a0003c0004t0004g0104a0003c0004t0004g0105 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.430+25035G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936868 | ||||||
| chr4:17936973
|
T | C | 1 | a0001c0001t0007g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.430+24930A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17936973 | ||||||
| chr4:17937022
|
A | G | 1 | a0001c0003t0003g0271 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.430+24881T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17937022 | ||||||
| chr4:17937182
|
T | C | 2 | a0004c0005t0008g0280a0004c0005t0008g0281 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.430+24721A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17937182 | ||||||
| chr4:17937679
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+24224A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17937679 | ||||||
| chr4:17937708
|
C | T | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+24195G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17937708 | ||||||
| chr4:17937812
|
C | T | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.430+24091G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17937812 | ||||||
| chr4:17938003
|
C | CT | 33 | a0001c0001t0001g0192a0001c0001t0002g0046a0001c0001t0002g0065others(30): Show | 33 | HG00639.hp2 HG00673.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.430+23899dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938003 | ||||||
| chr4:17938003
|
C | CTT | 71 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(68): Show | 72 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.430+23898_430+2389 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938003 | ||||||
| chr4:17938003
|
C | CTTT | 9 | a0001c0003t0003g0266a0002c0002t0020g0275a0002c0002t0020g0276others(6): Show | 9 | HG01358.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+23897_430+2389 others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938003 | ||||||
| chr4:17938034
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.430+23869G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938034 | ||||||
| chr4:17938068
|
C | T | 11 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+23835G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938068 | ||||||
| chr4:17938117
|
G | T | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+23786C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938117 | ||||||
| chr4:17938163
|
G | C | 1 | a0001c0001t0040g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.430+23740C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938163 | ||||||
| chr4:17938226
|
C | T | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.430+23677G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938226 | ||||||
| chr4:17938298
|
C | T | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+23605G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938298 | ||||||
| chr4:17938417
|
C | T | 1 | a0002c0002t0002g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.430+23486G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938417 | ||||||
| chr4:17938417
|
CT | C | 101 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(98): Show | 102 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(99): Show |
intron_variant | MODIFIER | c.430+23485delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938417 | ||||||
| chr4:17938435
|
A | G | 2 | a0003c0004t0004g0104a0003c0004t0004g0105 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.430+23468T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938435 | ||||||
| chr4:17938574
|
A | G | 83 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(80): Show | 84 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.430+23329T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938574 | ||||||
| chr4:17938604
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+23299A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938604 | ||||||
| chr4:17938913
|
C | T | 2 | a0004c0005t0008g0280a0004c0005t0008g0281 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.430+22990G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938913 | ||||||
| chr4:17938933
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.430+22970G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17938933 | ||||||
| chr4:17939095
|
C | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+22808G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939095 | ||||||
| chr4:17939251
|
C | G | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430+22652G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939251 | ||||||
| chr4:17939403
|
G | A | 1 | a0001c0001t0002g0049 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.430+22500C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939403 | ||||||
| chr4:17939404
|
G | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+22499C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939404 | ||||||
| chr4:17939432
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+22471A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939432 | ||||||
| chr4:17939879
|
T | TACACACA others(5): Show |
1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+22012_430+2202 others(16): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939879 | ||||||
| chr4:17939879
|
T | TACACACA others(7): Show |
38 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0233others(35): Show | 39 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.430+22010_430+2202 others(18): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939879 | ||||||
| chr4:17939879
|
T | TACACACA others(9): Show |
29 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0029g0232others(26): Show | 29 | HG00423.hp1 HG02055.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.430+22023_430+2202 others(20): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939879 | ||||||
| chr4:17939879
|
T | TACACACA others(11): Show |
6 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+22023_430+2202 others(22): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939879 | ||||||
| chr4:17939879
|
T | TACACACA others(19): Show |
1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.430+22023_430+2202 others(30): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939879 | ||||||
| chr4:17939879
|
T | TACGTACA others(11): Show |
1 | a0001c0003t0022g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.430+22023_430+2202 others(22): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939879 | ||||||
| chr4:17939923
|
C | T | 21 | a0001c0001t0001g0169a0003c0004t0002g0109a0003c0004t0004g0094others(18): Show | 21 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+21980G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939923 | ||||||
| chr4:17939940
|
T | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(86): Show | 90 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.430+21963A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939940 | ||||||
| chr4:17939946
|
C | A | 1 | a0002c0002t0002g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.430+21957G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17939946 | ||||||
| chr4:17940018
|
G | A | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430+21885C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940018 | ||||||
| chr4:17940019
|
C | T | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430+21884G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940019 | ||||||
| chr4:17940025
|
T | C | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430+21878A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940025 | ||||||
| chr4:17940076
|
T | C | 5 | a0001c0001t0007g0010a0001c0001t0007g0014a0001c0001t0007g0016others(2): Show | 5 | HG02895.hp2 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+21827A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940076 | ||||||
| chr4:17940116
|
G | GTA | 22 | a0001c0001t0001g0169a0001c0003t0003g0240a0003c0004t0002g0109others(19): Show | 22 | HG00673.hp1 HG02602.hp1 HG02602.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+21785_430+2178 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940116 | ||||||
| chr4:17940116
|
GTA | G | 10 | a0001c0001t0002g0049a0001c0001t0010g0228a0002c0002t0002g0027others(7): Show | 10 | HG01358.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+21785_430+2178 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940116 | ||||||
| chr4:17940134
|
G | GTGTATAT others(21): Show |
1 | a0004c0005t0030g0290 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.430+21768_430+2176 others(32): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940134 | ||||||
| chr4:17940134
|
G | GTGTATAT others(29): Show |
6 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0222others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+21733_430+2176 others(40): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940134 | ||||||
| chr4:17940136
|
G | GTATATAT others(31): Show |
14 | a0001c0001t0002g0046a0001c0001t0002g0065a0002c0002t0002g0006others(11): Show | 14 | HG01074.hp2 HG01258.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.430+21729_430+2176 others(42): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940136 | ||||||
| chr4:17940172
|
GTA | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0122others(154): Show | 159 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.430+21729_430+2173 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940172 | ||||||
| chr4:17940174
|
A | ATATATAT others(27): Show |
18 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(15): Show | 18 | HG02055.hp2 HG02615.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.430+21728_430+2172 others(38): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940174 | ||||||
| chr4:17940187
|
TAC | T | 3 | a0002c0002t0002g0004a0002c0002t0002g0071a0002c0002t0033g0070 | 3 | NA18986.hp2 NA19068.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.430+21714_430+2171 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940187 | ||||||
| chr4:17940201
|
T | C | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430+21702A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940201 | ||||||
| chr4:17940203
|
T | C | 10 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0283others(7): Show | 10 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+21700A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940203 | ||||||
| chr4:17940314
|
A | G | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+21589T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940314 | ||||||
| chr4:17940426
|
T | C | 1 | a0007c0008t0013g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.430+21477A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940426 | ||||||
| chr4:17940448
|
ATATGTAA others(7): Show |
A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.430+21441_430+2145 others(18): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940448 | ||||||
| chr4:17940452
|
G | A | 1 | a0007c0008t0013g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.430+21451C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940452 | ||||||
| chr4:17940569
|
T | A | 1 | a0001c0001t0019g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+21334A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940569 | ||||||
| chr4:17940640
|
T | C | 1 | a0002c0002t0005g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.430+21263A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940640 | ||||||
| chr4:17940650
|
C | T | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430+21253G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940650 | ||||||
| chr4:17940784
|
AT | A | 27 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(24): Show | 27 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.430+21118delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940784 | ||||||
| chr4:17940794
|
T | A | 1 | a0005c0006t0011g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.430+21109A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940794 | ||||||
| chr4:17940937
|
C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(200): Show | 205 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.430+20966G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940937 | ||||||
| chr4:17940962
|
T | A | 8 | a0001c0001t0009g0129a0001c0001t0009g0139a0001c0001t0009g0143others(5): Show | 8 | HG00423.hp2 HG00438.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+20941A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17940962 | ||||||
| chr4:17941063
|
A | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+20840T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941063 | ||||||
| chr4:17941152
|
A | G | 1 | a0001c0001t0009g0129 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.430+20751T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941152 | ||||||
| chr4:17941158
|
C | T | 4 | a0001c0001t0009g0139a0001c0001t0009g0164a0001c0001t0009g0166others(1): Show | 4 | HG00423.hp2 HG02132.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+20745G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941158 | ||||||
| chr4:17941174
|
A | C | 1 | a0001c0001t0001g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.430+20729T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941174 | ||||||
| chr4:17941184
|
G | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(84): Show | 88 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.430+20719C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941184 | ||||||
| chr4:17941268
|
C | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+20635G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941268 | ||||||
| chr4:17941488
|
T | A | 1 | a0002c0002t0002g0041 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.430+20415A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941488 | ||||||
| chr4:17941572
|
T | G | 1 | a0002c0002t0002g0036 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.430+20331A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941572 | ||||||
| chr4:17941852
|
A | AT | 6 | a0001c0003t0003g0216a0002c0002t0002g0036a0002c0002t0002g0039others(3): Show | 6 | HG01071.hp2 HG01975.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+20050dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941852 | ||||||
| chr4:17941852
|
AT | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(155): Show | 159 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(156): Show |
intron_variant | MODIFIER | c.430+20050delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17941852 | ||||||
| chr4:17942067
|
T | C | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.430+19836A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17942067 | ||||||
| chr4:17942190
|
G | A | 2 | a0001c0003t0003g0216a0001c0003t0003g0254 | 2 | HG02132.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.430+19713C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17942190 | ||||||
| chr4:17942387
|
A | G | 1 | a0002c0002t0002g0030 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.430+19516T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17942387 | ||||||
| chr4:17942672
|
G | A | 2 | a0010c0014t0015g0248a0010c0014t0015g0259 | 2 | HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.430+19231C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17942672 | ||||||
| chr4:17942755
|
G | A | 1 | a0012c0012t0003g0002 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.430+19148C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17942755 | ||||||
| chr4:17942879
|
G | GC | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+19023_430+1902 others(5): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17942879 | ||||||
| chr4:17942922
|
G | A | 2 | a0002c0002t0005g0116a0002c0002t0005g0117 | 2 | HG01081.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.430+18981C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17942922 | ||||||
| chr4:17942937
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.430+18966A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17942937 | ||||||
| chr4:17943076
|
A | G | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+18827T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17943076 | ||||||
| chr4:17943101
|
T | C | 2 | a0002c0002t0002g0027a0002c0002t0002g0069 | 2 | NA19007.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.430+18802A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17943101 | ||||||
| chr4:17943120
|
C | T | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+18783G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17943120 | ||||||
| chr4:17943217
|
G | A | 80 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(77): Show | 81 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.430+18686C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17943217 | ||||||
| chr4:17943601
|
T | TATTTCAC others(21): Show |
1 | a0001c0001t0001g0145 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.430+18274_430+1830 others(32): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17943601 | ||||||
| chr4:17943649
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.430+18254A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17943649 | ||||||
| chr4:17943747
|
G | A | 3 | a0002c0002t0002g0004a0002c0002t0002g0071a0002c0002t0033g0070 | 3 | NA18986.hp2 NA19068.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.430+18156C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17943747 | ||||||
| chr4:17943956
|
T | C | 4 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0029g0232others(1): Show | 4 | HG02896.hp1 HG03453.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+17947A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17943956 | ||||||
| chr4:17944056
|
A | G | 2 | a0002c0002t0002g0032a0002c0002t0002g0033 | 2 | NA18943.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.430+17847T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17944056 | ||||||
| chr4:17944455
|
G | C | 6 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+17448C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17944455 | ||||||
| chr4:17944552
|
G | A | 1 | a0002c0002t0005g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.430+17351C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17944552 | ||||||
| chr4:17944585
|
C | T | 3 | a0006c0007t0006g0274a0006c0007t0006g0277a0006c0007t0006g0278 | 3 | HG02451.hp1 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430+17318G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17944585 | ||||||
| chr4:17944809
|
T | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(190): Show | 195 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.430+17094A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17944809 | ||||||
| chr4:17945127
|
C | T | 6 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0222others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+16776G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945127 | ||||||
| chr4:17945334
|
C | G | 1 | a0005c0006t0011g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.430+16569G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945334 | ||||||
| chr4:17945411
|
G | GT | 28 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(25): Show | 28 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.430+16491dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945411 | ||||||
| chr4:17945411
|
G | T | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430+16492C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945411 | ||||||
| chr4:17945460
|
G | A | 1 | a0001c0003t0003g0253 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.430+16443C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945460 | ||||||
| chr4:17945803
|
G | A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.430+16100C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945803 | ||||||
| chr4:17945808
|
T | A | 3 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224 | 3 | HG02896.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.430+16095A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945808 | ||||||
| chr4:17945925
|
T | C | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.430+15978A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945925 | ||||||
| chr4:17945955
|
T | C | 3 | a0009c0009t0001g0178a0009c0009t0001g0186a0009c0009t0001g0187 | 3 | HG02056.hp2 NA18948.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.430+15948A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945955 | ||||||
| chr4:17945980
|
A | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+15923T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17945980 | ||||||
| chr4:17946019
|
C | A | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+15884G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946019 | ||||||
| chr4:17946078
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.430+15825A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946078 | ||||||
| chr4:17946250
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+15653A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946250 | ||||||
| chr4:17946422
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.430+15481T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946422 | ||||||
| chr4:17946427
|
T | A | 1 | a0002c0002t0002g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.430+15476A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946427 | ||||||
| chr4:17946466
|
T | A | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+15437A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946466 | ||||||
| chr4:17946716
|
A | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+15187T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946716 | ||||||
| chr4:17946729
|
G | A | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+15174C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946729 | ||||||
| chr4:17946861
|
A | G | 1 | a0005c0006t0011g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.430+15042T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946861 | ||||||
| chr4:17946874
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+15029A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946874 | ||||||
| chr4:17946942
|
C | T | 1 | a0004c0005t0008g0289 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.430+14961G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17946942 | ||||||
| chr4:17947045
|
A | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+14858T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17947045 | ||||||
| chr4:17947092
|
G | A | 1 | a0002c0002t0002g0071 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.430+14811C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17947092 | ||||||
| chr4:17947160
|
A | C | 1 | a0001c0001t0017g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.430+14743T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17947160 | ||||||
| chr4:17947316
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(86): Show | 90 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.430+14587A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17947316 | ||||||
| chr4:17947773
|
A | G | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430+14130T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17947773 | ||||||
| chr4:17947792
|
T | C | 1 | a0001c0003t0003g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.430+14111A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17947792 | ||||||
| chr4:17947984
|
A | G | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+13919T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17947984 | ||||||
| chr4:17948077
|
G | A | 6 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+13826C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17948077 | ||||||
| chr4:17948315
|
T | C | 1 | a0019c0019t0010g0221 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.430+13588A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17948315 | ||||||
| chr4:17948549
|
T | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+13354A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17948549 | ||||||
| chr4:17948724
|
A | T | 2 | a0003c0004t0004g0104a0003c0004t0004g0105 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.430+13179T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17948724 | ||||||
| chr4:17948756
|
A | T | 1 | a0002c0002t0005g0112 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.430+13147T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17948756 | ||||||
| chr4:17948802
|
A | AACAATTT others(16): Show |
1 | a0010c0014t0015g0259 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.430+13078_430+1310 others(27): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17948802 | ||||||
| chr4:17948891
|
AAG | A | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+13010_430+1301 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17948891 | ||||||
| chr4:17948954
|
G | A | 2 | a0001c0001t0001g0125a0003c0004t0004g0108 | 2 | HG01978.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.430+12949C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17948954 | ||||||
| chr4:17949003
|
A | G | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+12900T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949003 | ||||||
| chr4:17949018
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.430+12885A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949018 | ||||||
| chr4:17949203
|
C | T | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.430+12700G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949203 | ||||||
| chr4:17949227
|
T | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+12676A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949227 | ||||||
| chr4:17949345
|
G | A | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+12558C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949345 | ||||||
| chr4:17949409
|
T | C | 8 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(5): Show | 8 | HG01358.hp2 HG02451.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+12494A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949409 | ||||||
| chr4:17949412
|
A | G | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+12491T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949412 | ||||||
| chr4:17949591
|
T | G | 4 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0108others(1): Show | 4 | NA18961.hp2 NA18990.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+12312A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949591 | ||||||
| chr4:17949595
|
G | A | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430+12308C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949595 | ||||||
| chr4:17949745
|
G | A | 1 | a0001c0001t0023g0007 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.430+12158C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17949745 | ||||||
| chr4:17950114
|
T | C | 2 | a0001c0001t0009g0143a0001c0001t0024g0156 | 2 | NA18944.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.430+11789A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17950114 | ||||||
| chr4:17950282
|
G | T | 1 | a0002c0002t0002g0031 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.430+11621C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17950282 | ||||||
| chr4:17950414
|
T | C | 9 | a0002c0002t0002g0024a0002c0002t0002g0038a0002c0002t0002g0060others(6): Show | 9 | HG00642.hp1 HG01069.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+11489A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17950414 | ||||||
| chr4:17950433
|
G | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+11470C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17950433 | ||||||
| chr4:17950585
|
C | A | 2 | a0002c0002t0005g0116a0002c0002t0005g0117 | 2 | HG01081.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.430+11318G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17950585 | ||||||
| chr4:17950585
|
C | T | 80 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(77): Show | 81 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.430+11318G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17950585 | ||||||
| chr4:17950986
|
G | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+10917C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17950986 | ||||||
| chr4:17951004
|
T | G | 1 | a0002c0002t0012g0035 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.430+10899A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17951004 | ||||||
| chr4:17951162
|
C | G | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.430+10741G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17951162 | ||||||
| chr4:17951336
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+10567A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17951336 | ||||||
| chr4:17951667
|
T | C | 8 | a0003c0004t0004g0096a0003c0004t0004g0097a0003c0004t0004g0098others(5): Show | 8 | HG00673.hp1 HG02602.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+10236A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17951667 | ||||||
| chr4:17951779
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.430+10124G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17951779 | ||||||
| chr4:17951813
|
T | C | 1 | a0006c0007t0006g0272 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.430+10090A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17951813 | ||||||
| chr4:17951967
|
A | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+9936T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17951967 | ||||||
| chr4:17952033
|
A | T | 1 | a0015c0015t0003g0242 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.430+9870T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952033 | ||||||
| chr4:17952036
|
C | G | 1 | a0015c0015t0003g0242 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.430+9867G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952036 | ||||||
| chr4:17952041
|
C | T | 1 | a0015c0015t0003g0242 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.430+9862G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952041 | ||||||
| chr4:17952042
|
A | C | 1 | a0015c0015t0003g0242 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.430+9861T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952042 | ||||||
| chr4:17952043
|
G | T | 1 | a0015c0015t0003g0242 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.430+9860C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952043 | ||||||
| chr4:17952414
|
A | AT | 9 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0001t0001g0177others(6): Show | 9 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.430+9488dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952414 | ||||||
| chr4:17952414
|
AT | A | 37 | a0001c0001t0001g0181a0001c0001t0010g0226a0001c0001t0019g0204others(34): Show | 37 | HG01074.hp2 HG01099.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.430+9488delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952414 | ||||||
| chr4:17952457
|
C | T | 1 | a0002c0002t0002g0080 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.430+9446G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952457 | ||||||
| chr4:17952468
|
T | C | 3 | a0009c0009t0001g0178a0009c0009t0001g0186a0009c0009t0001g0187 | 3 | HG02056.hp2 NA18948.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.430+9435A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952468 | ||||||
| chr4:17952473
|
T | A | 1 | a0002c0002t0002g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.430+9430A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952473 | ||||||
| chr4:17952745
|
G | A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.430+9158C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952745 | ||||||
| chr4:17952966
|
C | G | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430+8937G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17952966 | ||||||
| chr4:17953197
|
C | A | 3 | a0001c0001t0018g0174a0001c0001t0018g0175a0004c0005t0004g0220 | 3 | HG02886.hp1 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.430+8706G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17953197 | ||||||
| chr4:17953199
|
A | G | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+8704T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17953199 | ||||||
| chr4:17953619
|
C | A | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430+8284G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17953619 | ||||||
| chr4:17953675
|
T | C | 6 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0222others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+8228A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17953675 | ||||||
| chr4:17953970
|
T | C | 2 | a0004c0005t0008g0283a0004c0005t0030g0290 | 2 | HG02145.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.430+7933A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17953970 | ||||||
| chr4:17954394
|
T | C | 80 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(77): Show | 81 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.430+7509A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17954394 | ||||||
| chr4:17954581
|
T | C | 2 | a0001c0001t0017g0198a0001c0001t0017g0199 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.430+7322A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17954581 | ||||||
| chr4:17954590
|
TG | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0089others(200): Show | 205 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.430+7312delC | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17954590 | ||||||
| chr4:17954641
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.430+7262A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17954641 | ||||||
| chr4:17954766
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.430+7137C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17954766 | ||||||
| chr4:17954972
|
G | A | 6 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0222others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+6931C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17954972 | ||||||
| chr4:17955034
|
T | C | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+6869A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955034 | ||||||
| chr4:17955105
|
C | T | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430+6798G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955105 | ||||||
| chr4:17955135
|
A | C | 1 | a0003c0004t0004g0110 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.430+6768T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955135 | ||||||
| chr4:17955220
|
A | C | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430+6683T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955220 | ||||||
| chr4:17955241
|
C | T | 3 | a0001c0003t0003g0236a0001c0003t0003g0237a0001c0003t0003g0258 | 3 | HG01243.hp2 HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.430+6662G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955241 | ||||||
| chr4:17955281
|
T | C | 1 | a0006c0007t0006g0272 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.430+6622A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955281 | ||||||
| chr4:17955535
|
G | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+6368C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955535 | ||||||
| chr4:17955577
|
T | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+6326A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955577 | ||||||
| chr4:17955656
|
T | C | 2 | a0001c0003t0003g0266a0001c0003t0003g0271 | 2 | HG01099.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.430+6247A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955656 | ||||||
| chr4:17955731
|
G | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+6172C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955731 | ||||||
| chr4:17955732
|
T | C | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.430+6171A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955732 | ||||||
| chr4:17955953
|
C | T | 77 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(74): Show | 78 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.430+5950G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17955953 | ||||||
| chr4:17956034
|
G | A | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.430+5869C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17956034 | ||||||
| chr4:17956065
|
T | A | 52 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(49): Show | 53 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.430+5838A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17956065 | ||||||
| chr4:17956073
|
C | T | 1 | a0001c0001t0027g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.430+5830G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17956073 | ||||||
| chr4:17956075
|
C | T | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+5828G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17956075 | ||||||
| chr4:17956220
|
T | C | 1 | a0003c0004t0004g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.430+5683A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17956220 | ||||||
| chr4:17956415
|
T | C | 2 | a0002c0002t0002g0022a0002c0002t0002g0023 | 2 | NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.430+5488A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17956415 | ||||||
| chr4:17956723
|
G | C | 1 | a0001c0003t0003g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.430+5180C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17956723 | ||||||
| chr4:17956828
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0169 | 3 | NA18942.hp1 NA18964.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.430+5075A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17956828 | ||||||
| chr4:17956982
|
A | G | 2 | a0014c0011t0004g0092a0014c0011t0004g0093 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.430+4921T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17956982 | ||||||
| chr4:17957034
|
G | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.430+4869C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17957034 | ||||||
| chr4:17957067
|
C | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.430+4836G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17957067 | ||||||
| chr4:17957140
|
G | A | 2 | a0002c0002t0014g0212a0002c0002t0014g0213 | 2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.430+4763C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17957140 | ||||||
| chr4:17957444
|
T | C | 1 | a0003c0004t0004g0110 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.430+4459A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17957444 | ||||||
| chr4:17957567
|
T | C | 1 | a0002c0002t0012g0051 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.430+4336A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17957567 | ||||||
| chr4:17957655
|
T | C | 5 | a0002c0002t0002g0036a0002c0002t0002g0037a0002c0002t0002g0039others(2): Show | 5 | HG01071.hp2 HG01975.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+4248A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17957655 | ||||||
| chr4:17957933
|
G | C | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+3970C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17957933 | ||||||
| chr4:17957953
|
A | G | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.430+3950T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17957953 | ||||||
| chr4:17957958
|
C | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+3945G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17957958 | ||||||
| chr4:17958153
|
C | T | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+3750G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17958153 | ||||||
| chr4:17958356
|
C | A | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.430+3547G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17958356 | ||||||
| chr4:17958385
|
T | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+3518A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17958385 | ||||||
| chr4:17958545
|
G | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+3358C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17958545 | ||||||
| chr4:17958631
|
A | C | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430+3272T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17958631 | ||||||
| chr4:17959246
|
C | A | 2 | a0002c0002t0002g0080a0002c0002t0002g0081 | 2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.430+2657G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17959246 | ||||||
| chr4:17959294
|
T | C | 1 | a0001c0003t0003g0247 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.430+2609A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17959294 | ||||||
| chr4:17959378
|
T | A | 1 | a0002c0002t0012g0035 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.430+2525A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17959378 | ||||||
| chr4:17959379
|
T | A | 1 | a0002c0002t0012g0035 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.430+2524A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17959379 | ||||||
| chr4:17959491
|
T | G | 3 | a0001c0003t0003g0238a0001c0003t0003g0251a0001c0003t0003g0253 | 3 | HG00639.hp1 HG01192.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.430+2412A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17959491 | ||||||
| chr4:17959754
|
A | G | 4 | a0001c0003t0003g0236a0001c0003t0003g0237a0001c0003t0003g0258others(1): Show | 4 | HG01243.hp2 HG02040.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2149T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17959754 | ||||||
| chr4:17959788
|
G | C | 1 | a0002c0002t0005g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.430+2115C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17959788 | ||||||
| chr4:17959792
|
G | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+2111C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17959792 | ||||||
| chr4:17959862
|
C | T | 1 | a0002c0002t0002g0080 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.430+2041G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17959862 | ||||||
| chr4:17960095
|
T | A | 1 | a0015c0015t0003g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.430+1808A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17960095 | ||||||
| chr4:17960249
|
A | T | 2 | a0002c0002t0020g0275a0002c0002t0020g0276 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.430+1654T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17960249 | ||||||
| chr4:17960420
|
T | C | 1 | a0003c0004t0004g0127 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.430+1483A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17960420 | ||||||
| chr4:17960510
|
A | G | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430+1393T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17960510 | ||||||
| chr4:17960637
|
G | A | 77 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(74): Show | 78 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.430+1266C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17960637 | ||||||
| chr4:17960726
|
G | A | 1 | a0003c0004t0004g0110 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.430+1177C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17960726 | ||||||
| chr4:17960756
|
A | G | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+1147T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17960756 | ||||||
| chr4:17960910
|
A | AC | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+992_430+993ins others(1): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17960910 | ||||||
| chr4:17960919
|
T | C | 25 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(22): Show | 25 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.430+984A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17960919 | ||||||
| chr4:17961061
|
C | T | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+842G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17961061 | ||||||
| chr4:17961312
|
A | T | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.430+591T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17961312 | ||||||
| chr4:17961424
|
C | G | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.430+479G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17961424 | ||||||
| chr4:17961453
|
T | C | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+450A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 4/7 | chr4 | 17961453 | ||||||
| chr4:17962221
|
T | A | 1 | a0001c0001t0001g0207 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.301-189A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 3/7 | chr4 | 17962221 | ||||||
| chr4:17962255
|
CA | C | 8 | a0001c0001t0002g0065a0001c0001t0009g0164a0001c0001t0010g0226others(5): Show | 8 | HG02071.hp2 HG02080.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.301-224delT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 3/7 | chr4 | 17962255 | ||||||
| chr4:17962755
|
T | TA | 11 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.300+214dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 3/7 | chr4 | 17962755 | ||||||
| chr4:17962905
|
T | TA | 10 | a0001c0001t0009g0143a0001c0001t0018g0174a0001c0001t0018g0175others(7): Show | 10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.300+64dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 3/7 | chr4 | 17962905 | ||||||
| chr4:17962916
|
C | A | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.300+54G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 3/7 | chr4 | 17962916 | ||||||
| chr4:17963303
|
A | G | 27 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(24): Show | 27 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.221-254T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17963303 | ||||||
| chr4:17963354
|
G | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.221-305C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17963354 | ||||||
| chr4:17963458
|
G | C | 1 | a0001c0001t0001g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.221-409C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17963458 | ||||||
| chr4:17963526
|
C | A | 1 | a0001c0001t0027g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.221-477G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17963526 | ||||||
| chr4:17963641
|
AT | A | 82 | a0001c0001t0001g0179a0001c0001t0010g0226a0001c0001t0010g0228others(79): Show | 83 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.221-593delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17963641 | ||||||
| chr4:17963869
|
C | A | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.221-820G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17963869 | ||||||
| chr4:17963952
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.221-903C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17963952 | ||||||
| chr4:17964102
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.221-1053A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964102 | ||||||
| chr4:17964214
|
G | A | 1 | a0003c0004t0004g0097 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.221-1165C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964214 | ||||||
| chr4:17964304
|
A | C | 8 | a0002c0002t0002g0024a0002c0002t0002g0038a0002c0002t0002g0060others(5): Show | 8 | HG00642.hp1 HG01069.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-1255T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964304 | ||||||
| chr4:17964458
|
T | C | 13 | a0001c0001t0005g0114a0002c0002t0005g0111a0002c0002t0005g0112others(10): Show | 13 | HG01081.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.221-1409A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964458 | ||||||
| chr4:17964497
|
A | G | 12 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0147others(9): Show | 13 | HG01975.hp1 HG02080.hp1 HG03834.hp1 others(10): Show |
intron_variant | MODIFIER | c.221-1448T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964497 | ||||||
| chr4:17964515
|
T | G | 1 | a0001c0001t0001g0136 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.221-1466A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964515 | ||||||
| chr4:17964647
|
C | T | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.221-1598G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964647 | ||||||
| chr4:17964845
|
G | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.221-1796C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964845 | ||||||
| chr4:17964863
|
G | GC | 75 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(72): Show | 76 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.221-1815dupG | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964863 | ||||||
| chr4:17964867
|
T | C | 31 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(28): Show | 31 | HG01258.hp2 HG01891.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.221-1818A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964867 | ||||||
| chr4:17964868
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.221-1819A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964868 | ||||||
| chr4:17964925
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(88): Show | 92 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.221-1876A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964925 | ||||||
| chr4:17964938
|
G | C | 1 | a0001c0001t0001g0194 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.221-1889C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17964938 | ||||||
| chr4:17965094
|
C | A | 1 | a0003c0004t0004g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.221-2045G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965094 | ||||||
| chr4:17965123
|
T | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.221-2074A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965123 | ||||||
| chr4:17965329
|
C | A | 1 | a0003c0004t0004g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.221-2280G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965329 | ||||||
| chr4:17965471
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.221-2422A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965471 | ||||||
| chr4:17965491
|
G | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.221-2442C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965491 | ||||||
| chr4:17965609
|
T | G | 1 | a0001c0001t0001g0177 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.221-2560A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965609 | ||||||
| chr4:17965642
|
T | C | 4 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0229others(1): Show | 4 | HG02145.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-2593A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965642 | ||||||
| chr4:17965672
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.221-2623G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965672 | ||||||
| chr4:17965678
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.221-2629A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965678 | ||||||
| chr4:17965703
|
T | C | 3 | a0002c0002t0002g0004a0002c0002t0002g0071a0002c0002t0033g0070 | 3 | NA18986.hp2 NA19068.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.221-2654A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965703 | ||||||
| chr4:17965837
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.221-2788A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17965837 | ||||||
| chr4:17966161
|
G | C | 8 | a0002c0002t0002g0024a0002c0002t0002g0038a0002c0002t0002g0060others(5): Show | 8 | HG00642.hp1 HG01069.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-3112C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966161 | ||||||
| chr4:17966273
|
G | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.221-3224C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966273 | ||||||
| chr4:17966335
|
G | A | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.221-3286C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966335 | ||||||
| chr4:17966542
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.221-3493A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966542 | ||||||
| chr4:17966545
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.221-3496A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966545 | ||||||
| chr4:17966677
|
C | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(278): Show | 283 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(280): Show |
intron_variant | MODIFIER | c.221-3628G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966677 | ||||||
| chr4:17966793
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0146 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.221-3744A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966793 | ||||||
| chr4:17966796
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.221-3747A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966796 | ||||||
| chr4:17966909
|
A | G | 3 | a0004c0005t0008g0286a0004c0005t0008g0287a0004c0005t0008g0288 | 3 | HG02965.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.221-3860T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966909 | ||||||
| chr4:17966967
|
G | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.221-3918C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17966967 | ||||||
| chr4:17967098
|
C | T | 12 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(9): Show | 12 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-4049G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17967098 | ||||||
| chr4:17967188
|
T | A | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.221-4139A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17967188 | ||||||
| chr4:17967519
|
T | G | 3 | a0001c0001t0036g0075a0002c0002t0002g0076a0002c0002t0002g0077 | 3 | HG01123.hp2 HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.221-4470A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17967519 | ||||||
| chr4:17967589
|
T | C | 1 | a0001c0001t0018g0175 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.221-4540A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17967589 | ||||||
| chr4:17967830
|
T | A | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.221-4781A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17967830 | ||||||
| chr4:17967960
|
C | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.220+4860G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17967960 | ||||||
| chr4:17968075
|
T | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(170): Show | 175 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.220+4745A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17968075 | ||||||
| chr4:17968518
|
T | C | 1 | a0001c0003t0022g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.220+4302A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17968518 | ||||||
| chr4:17968640
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(190): Show | 195 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.220+4180G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17968640 | ||||||
| chr4:17968703
|
A | T | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.220+4117T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17968703 | ||||||
| chr4:17968826
|
C | T | 1 | a0002c0002t0002g0027 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.220+3994G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17968826 | ||||||
| chr4:17968930
|
C | T | 2 | a0001c0003t0003g0262a0001c0003t0003g0263 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.220+3890G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17968930 | ||||||
| chr4:17969032
|
C | T | 83 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(80): Show | 84 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.220+3788G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17969032 | ||||||
| chr4:17969227
|
T | C | 1 | a0023c0016t0004g0091 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.220+3593A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17969227 | ||||||
| chr4:17969515
|
A | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.220+3305T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17969515 | ||||||
| chr4:17969586
|
C | T | 3 | a0001c0003t0003g0236a0001c0003t0003g0237a0001c0003t0003g0258 | 3 | HG01243.hp2 HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.220+3234G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17969586 | ||||||
| chr4:17969924
|
G | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.220+2896C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17969924 | ||||||
| chr4:17969988
|
C | T | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.220+2832G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17969988 | ||||||
| chr4:17970455
|
C | A | 80 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(77): Show | 81 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.220+2365G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17970455 | ||||||
| chr4:17970659
|
G | A | 1 | a0002c0026t0005g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220+2161C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17970659 | ||||||
| chr4:17970749
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(165): Show | 170 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.220+2071C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17970749 | ||||||
| chr4:17970872
|
G | A | 1 | a0005c0006t0011g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.220+1948C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17970872 | ||||||
| chr4:17971139
|
CAT | C | 8 | a0001c0001t0001g0182a0002c0002t0020g0275a0002c0002t0020g0276others(5): Show | 8 | HG01358.hp2 HG01515.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.220+1679_220+1680d others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17971139 | ||||||
| chr4:17971441
|
T | A | 1 | a0001c0001t0036g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.220+1379A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17971441 | ||||||
| chr4:17971548
|
G | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.220+1272C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17971548 | ||||||
| chr4:17971549
|
T | C | 4 | a0001c0001t0012g0062a0002c0002t0012g0035a0002c0002t0012g0051others(1): Show | 4 | HG00438.hp2 NA18942.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+1271A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17971549 | ||||||
| chr4:17971594
|
G | A | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.220+1226C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17971594 | ||||||
| chr4:17971670
|
C | T | 22 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(19): Show | 22 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(19): Show |
intron_variant | MODIFIER | c.220+1150G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17971670 | ||||||
| chr4:17971863
|
A | G | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.220+957T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17971863 | ||||||
| chr4:17971936
|
T | A | 3 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224 | 3 | HG02896.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.220+884A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17971936 | ||||||
| chr4:17972075
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.220+745A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17972075 | ||||||
| chr4:17972276
|
C | G | 83 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(80): Show | 84 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.220+544G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17972276 | ||||||
| chr4:17972287
|
A | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.220+533T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17972287 | ||||||
| chr4:17972432
|
T | C | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.220+388A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17972432 | ||||||
| chr4:17972511
|
A | T | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+309T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17972511 | ||||||
| chr4:17972558
|
A | G | 83 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(80): Show | 84 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.220+262T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17972558 | ||||||
| chr4:17972596
|
A | G | 37 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(34): Show | 38 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.220+224T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17972596 | ||||||
| chr4:17972716
|
G | T | 1 | a0003c0004t0004g0107 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.220+104C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 2/7 | chr4 | 17972716 | ||||||
| chr4:17973135
|
T | A | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.155-250A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17973135 | ||||||
| chr4:17973137
|
A | G | 1 | a0003c0004t0004g0097 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.155-252T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17973137 | ||||||
| chr4:17973260
|
T | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-375A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17973260 | ||||||
| chr4:17973386
|
T | C | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.155-501A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17973386 | ||||||
| chr4:17973444
|
C | T | 1 | a0001c0001t0027g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.155-559G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17973444 | ||||||
| chr4:17973758
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.155-873A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17973758 | ||||||
| chr4:17973980
|
C | T | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-1095G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17973980 | ||||||
| chr4:17974052
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.155-1167G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974052 | ||||||
| chr4:17974322
|
ACTT | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0169 | 3 | NA18942.hp1 NA18964.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.155-1440_155-1438d others(5): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974322 | ||||||
| chr4:17974418
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-1533A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974418 | ||||||
| chr4:17974703
|
A | G | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-1818T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974703 | ||||||
| chr4:17974721
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.155-1836A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974721 | ||||||
| chr4:17974855
|
T | C | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.155-1970A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974855 | ||||||
| chr4:17974874
|
A | C | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.155-1989T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974874 | ||||||
| chr4:17974953
|
T | C | 27 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(24): Show | 27 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-2068A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974953 | ||||||
| chr4:17974989
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-2104A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974989 | ||||||
| chr4:17974993
|
G | A | 1 | a0001c0003t0003g0252 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.155-2108C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17974993 | ||||||
| chr4:17975156
|
A | G | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-2271T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975156 | ||||||
| chr4:17975223
|
C | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-2338G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975223 | ||||||
| chr4:17975374
|
G | A | 1 | a0001c0001t0029g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.155-2489C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975374 | ||||||
| chr4:17975445
|
G | A | 9 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0149others(6): Show | 9 | HG01433.hp2 HG01928.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-2560C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975445 | ||||||
| chr4:17975499
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.155-2614C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975499 | ||||||
| chr4:17975524
|
G | A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.155-2639C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975524 | ||||||
| chr4:17975599
|
T | A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.155-2714A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975599 | ||||||
| chr4:17975729
|
T | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(86): Show | 90 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.155-2844A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975729 | ||||||
| chr4:17975808
|
T | C | 4 | a0001c0001t0001g0147a0001c0001t0001g0162a0001c0001t0001g0170others(1): Show | 4 | HG01975.hp1 NA18943.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-2923A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975808 | ||||||
| chr4:17975888
|
T | C | 6 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-3003A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975888 | ||||||
| chr4:17975912
|
A | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-3027T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17975912 | ||||||
| chr4:17976052
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.155-3167T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17976052 | ||||||
| chr4:17976256
|
A | T | 2 | a0002c0002t0020g0275a0002c0002t0020g0276 | 2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.155-3371T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17976256 | ||||||
| chr4:17976350
|
C | T | 1 | a0003c0004t0004g0107 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.155-3465G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17976350 | ||||||
| chr4:17976446
|
C | T | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.155-3561G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17976446 | ||||||
| chr4:17976569
|
T | C | 1 | a0002c0002t0005g0117 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.155-3684A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17976569 | ||||||
| chr4:17976704
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.155-3819G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17976704 | ||||||
| chr4:17976829
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.155-3944A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17976829 | ||||||
| chr4:17976855
|
G | A | 1 | a0002c0002t0002g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.155-3970C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17976855 | ||||||
| chr4:17977266
|
T | C | 2 | a0001c0001t0017g0198a0001c0001t0017g0199 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.155-4381A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977266 | ||||||
| chr4:17977269
|
A | T | 194 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(191): Show | 196 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.155-4384T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977269 | ||||||
| chr4:17977340
|
A | G | 2 | a0005c0006t0005g0231a0005c0006t0011g0229 | 2 | HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.155-4455T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977340 | ||||||
| chr4:17977373
|
G | A | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.155-4488C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977373 | ||||||
| chr4:17977393
|
C | G | 2 | a0003c0004t0004g0104a0003c0004t0004g0105 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.155-4508G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977393 | ||||||
| chr4:17977459
|
A | T | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.155-4574T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977459 | ||||||
| chr4:17977622
|
A | C | 1 | a0003c0004t0004g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.155-4737T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977622 | ||||||
| chr4:17977812
|
G | A | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.155-4927C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977812 | ||||||
| chr4:17977900
|
C | T | 1 | a0003c0004t0004g0119 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.155-5015G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977900 | ||||||
| chr4:17977947
|
T | A | 1 | a0002c0002t0005g0112 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.155-5062A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977947 | ||||||
| chr4:17977970
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-5085A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17977970 | ||||||
| chr4:17978010
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.155-5125T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978010 | ||||||
| chr4:17978187
|
T | C | 3 | a0008c0010t0001g0189a0008c0010t0001g0190a0008c0010t0001g0197 | 3 | HG01069.hp1 HG01071.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.155-5302A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978187 | ||||||
| chr4:17978206
|
T | C | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.155-5321A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978206 | ||||||
| chr4:17978221
|
T | G | 1 | a0006c0007t0006g0250 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.155-5336A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978221 | ||||||
| chr4:17978245
|
T | C | 1 | a0002c0002t0002g0071 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.155-5360A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978245 | ||||||
| chr4:17978360
|
G | A | 2 | a0004c0005t0010g0227a0019c0019t0010g0221 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.155-5475C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978360 | ||||||
| chr4:17978536
|
G | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-5651C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978536 | ||||||
| chr4:17978579
|
C | CAA | 29 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(26): Show | 29 | HG01169.hp1 HG01891.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.155-5696_155-5695d others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978579 | ||||||
| chr4:17978579
|
C | CAAA | 51 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(48): Show | 52 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.155-5697_155-5695d others(5): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978579 | ||||||
| chr4:17978656
|
A | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-5771T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978656 | ||||||
| chr4:17978869
|
A | G | 2 | a0001c0003t0003g0214a0001c0003t0003g0260 | 2 | NA18946.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.155-5984T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978869 | ||||||
| chr4:17978959
|
C | T | 4 | a0002c0002t0002g0054a0002c0002t0002g0055a0002c0002t0002g0056others(1): Show | 4 | HG00673.hp2 HG02083.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-6074G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17978959 | ||||||
| chr4:17979012
|
G | A | 1 | a0002c0002t0005g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.155-6127C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17979012 | ||||||
| chr4:17979101
|
T | C | 1 | a0002c0002t0001g0085 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.155-6216A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17979101 | ||||||
| chr4:17979393
|
T | A | 1 | a0001c0001t0002g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.155-6508A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17979393 | ||||||
| chr4:17979438
|
T | C | 1 | a0015c0015t0003g0242 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.155-6553A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17979438 | ||||||
| chr4:17979664
|
A | G | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.155-6779T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17979664 | ||||||
| chr4:17979768
|
G | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.155-6883C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17979768 | ||||||
| chr4:17980062
|
C | T | 5 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0274others(2): Show | 5 | HG02451.hp1 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-7177G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17980062 | ||||||
| chr4:17980063
|
G | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-7178C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17980063 | ||||||
| chr4:17980256
|
C | G | 1 | a0002c0002t0005g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.155-7371G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17980256 | ||||||
| chr4:17980262
|
G | T | 1 | a0002c0002t0002g0080 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.155-7377C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17980262 | ||||||
| chr4:17980385
|
C | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-7500G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17980385 | ||||||
| chr4:17980758
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.155-7873T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17980758 | ||||||
| chr4:17980795
|
T | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-7910A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17980795 | ||||||
| chr4:17980829
|
G | A | 1 | a0002c0002t0005g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.155-7944C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17980829 | ||||||
| chr4:17981089
|
A | G | 1 | a0002c0002t0002g0029 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.155-8204T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17981089 | ||||||
| chr4:17981432
|
G | A | 73 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(70): Show | 74 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.155-8547C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17981432 | ||||||
| chr4:17981495
|
G | A | 3 | a0002c0002t0002g0009a0002c0002t0002g0034a0002c0002t0002g0047 | 3 | NA18944.hp1 NA18946.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.155-8610C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17981495 | ||||||
| chr4:17981668
|
G | T | 1 | a0002c0002t0005g0113 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.155-8783C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17981668 | ||||||
| chr4:17981971
|
T | C | 1 | a0001c0003t0003g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.155-9086A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17981971 | ||||||
| chr4:17982099
|
C | CGT | 34 | a0001c0001t0001g0068a0001c0001t0001g0179a0001c0001t0002g0065others(31): Show | 35 | HG00735.hp2 HG00738.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.155-9216_155-9215d others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
C | CGTGT | 27 | a0001c0003t0003g0215a0001c0003t0003g0246a0001c0003t0003g0249others(24): Show | 27 | HG00639.hp1 HG00673.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-9218_155-9215d others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
C | CGTGTGT | 21 | a0001c0001t0007g0014a0001c0001t0007g0016a0001c0001t0007g0017others(18): Show | 21 | HG01081.hp1 HG01169.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.155-9220_155-9215d others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
C | CGTGTGTG others(1): Show |
14 | a0001c0003t0003g0216a0001c0003t0003g0236a0001c0003t0003g0237others(11): Show | 14 | HG01123.hp2 HG02129.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.155-9222_155-9215d others(10): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
C | CGTGTGTG others(3): Show |
6 | a0001c0003t0003g0257a0001c0003t0003g0268a0001c0003t0003g0271others(3): Show | 6 | HG00423.hp1 HG01099.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-9224_155-9215d others(12): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
C | CGTGTGTG others(5): Show |
6 | a0002c0002t0038g0013a0003c0004t0004g0110a0004c0020t0032g0279others(3): Show | 6 | HG01358.hp2 HG01891.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-9226_155-9215d others(14): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
CGT | C | 19 | a0001c0001t0001g0149a0001c0001t0001g0158a0001c0001t0001g0192others(16): Show | 19 | HG00438.hp2 HG01106.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.155-9216_155-9215d others(4): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
CGTGT | C | 41 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0125others(38): Show | 41 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.155-9218_155-9215d others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
CGTGTGT | C | 63 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(60): Show | 64 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.155-9220_155-9215d others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
CGTGTGTG others(1): Show |
C | 16 | a0001c0001t0001g0172a0001c0001t0001g0201a0001c0001t0029g0232others(13): Show | 16 | HG00673.hp2 HG01346.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.155-9222_155-9215d others(10): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
CGTGTGTG others(3): Show |
C | 3 | a0001c0001t0001g0132a0001c0001t0019g0133a0001c0001t0019g0204 | 3 | HG02717.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.155-9224_155-9215d others(12): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
CGTGTGTG others(5): Show |
C | 2 | a0002c0002t0002g0063a0002c0002t0002g0066 | 2 | HG00642.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.155-9226_155-9215d others(14): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
CGTGTGTG others(7): Show |
C | 1 | a0002c0026t0005g0115 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.155-9228_155-9215d others(16): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982099
|
CGTGTGTG others(15): Show |
C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.155-9236_155-9215d others(24): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982099 | ||||||
| chr4:17982143
|
T | C | 3 | a0002c0002t0014g0211a0002c0002t0014g0212a0002c0002t0014g0213 | 3 | HG01891.hp2 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.155-9258A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982143 | ||||||
| chr4:17982202
|
T | C | 1 | a0001c0003t0003g0270 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.155-9317A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982202 | ||||||
| chr4:17982213
|
T | C | 1 | a0003c0004t0004g0108 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.155-9328A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982213 | ||||||
| chr4:17982495
|
T | C | 1 | a0001c0001t0029g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.155-9610A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982495 | ||||||
| chr4:17982506
|
T | G | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-9621A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982506 | ||||||
| chr4:17982520
|
T | TA | 193 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(190): Show | 195 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.155-9636dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982520 | ||||||
| chr4:17982598
|
C | T | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.155-9713G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982598 | ||||||
| chr4:17982607
|
C | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-9722G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982607 | ||||||
| chr4:17982654
|
T | C | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-9769A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982654 | ||||||
| chr4:17982693
|
A | C | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-9808T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982693 | ||||||
| chr4:17982718
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.155-9833A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982718 | ||||||
| chr4:17982729
|
T | C | 1 | a0002c0002t0002g0019 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.155-9844A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982729 | ||||||
| chr4:17982743
|
T | C | 1 | a0003c0004t0004g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.155-9858A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982743 | ||||||
| chr4:17982839
|
C | A | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-9954G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17982839 | ||||||
| chr4:17983219
|
G | T | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-10334C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983219 | ||||||
| chr4:17983251
|
C | G | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-10366G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983251 | ||||||
| chr4:17983377
|
T | C | 3 | a0001c0003t0003g0267a0001c0003t0003g0268a0001c0003t0003g0269 | 3 | HG02056.hp1 HG02129.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.155-10492A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983377 | ||||||
| chr4:17983478
|
C | T | 1 | a0002c0002t0002g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.155-10593G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983478 | ||||||
| chr4:17983502
|
C | T | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.155-10617G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983502 | ||||||
| chr4:17983566
|
T | C | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-10681A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983566 | ||||||
| chr4:17983588
|
T | G | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-10703A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983588 | ||||||
| chr4:17983602
|
G | A | 24 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224others(21): Show | 24 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(21): Show |
intron_variant | MODIFIER | c.155-10717C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983602 | ||||||
| chr4:17983605
|
CATTGCTT others(4): Show |
C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-10731_155-1072 others(15): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983605 | ||||||
| chr4:17983703
|
A | G | 2 | a0001c0003t0003g0262a0001c0003t0003g0263 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.155-10818T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983703 | ||||||
| chr4:17983751
|
T | C | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-10866A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983751 | ||||||
| chr4:17983811
|
A | G | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.155-10926T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983811 | ||||||
| chr4:17983904
|
T | C | 1 | a0004c0005t0030g0290 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.155-11019A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983904 | ||||||
| chr4:17983991
|
C | T | 4 | a0002c0002t0002g0036a0002c0002t0002g0039a0002c0002t0002g0053others(1): Show | 4 | HG01071.hp2 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-11106G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983991 | ||||||
| chr4:17983993
|
T | C | 3 | a0002c0002t0005g0116a0002c0002t0005g0117a0002c0026t0005g0115 | 3 | HG01081.hp2 HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.155-11108A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17983993 | ||||||
| chr4:17984329
|
T | C | 1 | a0003c0004t0004g0103 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.155-11444A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17984329 | ||||||
| chr4:17984385
|
A | G | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.155-11500T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17984385 | ||||||
| chr4:17984499
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.155-11614C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17984499 | ||||||
| chr4:17984561
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0146 | 2 | HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.155-11676C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17984561 | ||||||
| chr4:17984899
|
C | T | 77 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(74): Show | 78 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.155-12014G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17984899 | ||||||
| chr4:17984942
|
C | T | 7 | a0002c0002t0002g0028a0002c0002t0002g0030a0002c0002t0002g0031others(4): Show | 7 | NA18943.hp1 NA18949.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.155-12057G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17984942 | ||||||
| chr4:17985050
|
G | A | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.155-12165C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985050 | ||||||
| chr4:17985104
|
T | C | 1 | a0012c0012t0003g0002 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.155-12219A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985104 | ||||||
| chr4:17985143
|
T | C | 1 | a0018c0021t0004g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.155-12258A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985143 | ||||||
| chr4:17985239
|
A | G | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0158others(2): Show | 5 | NA18969.hp1 NA18990.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-12354T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985239 | ||||||
| chr4:17985240
|
T | C | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-12355A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985240 | ||||||
| chr4:17985509
|
C | A | 1 | a0001c0001t0001g0147 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.155-12624G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985509 | ||||||
| chr4:17985578
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.155-12693G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985578 | ||||||
| chr4:17985632
|
T | C | 1 | a0003c0004t0004g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.155-12747A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985632 | ||||||
| chr4:17985705
|
T | C | 1 | a0001c0001t0027g0142 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.155-12820A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985705 | ||||||
| chr4:17985760
|
C | T | 2 | a0001c0003t0003g0215a0001c0003t0003g0245 | 2 | NA19005.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.155-12875G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985760 | ||||||
| chr4:17985840
|
T | C | 24 | a0001c0001t0010g0228a0001c0001t0029g0232a0004c0005t0004g0220others(21): Show | 24 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.155-12955A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985840 | ||||||
| chr4:17985981
|
C | T | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-13096G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17985981 | ||||||
| chr4:17986171
|
T | C | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.155-13286A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17986171 | ||||||
| chr4:17986193
|
A | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-13308T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17986193 | ||||||
| chr4:17986518
|
A | G | 80 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0228others(77): Show | 81 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.155-13633T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17986518 | ||||||
| chr4:17986667
|
G | A | 2 | a0004c0005t0008g0280a0004c0005t0008g0281 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.155-13782C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17986667 | ||||||
| chr4:17987012
|
T | A | 75 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(72): Show | 76 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.155-14127A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17987012 | ||||||
| chr4:17987038
|
G | A | 1 | a0002c0002t0002g0027 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.155-14153C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17987038 | ||||||
| chr4:17987107
|
C | T | 1 | a0002c0002t0005g0209 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.155-14222G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17987107 | ||||||
| chr4:17987352
|
T | C | 1 | a0001c0001t0002g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.155-14467A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17987352 | ||||||
| chr4:17987435
|
A | G | 1 | a0001c0001t0016g0140 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.155-14550T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17987435 | ||||||
| chr4:17987968
|
T | C | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.155-15083A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17987968 | ||||||
| chr4:17988179
|
T | A | 1 | a0003c0004t0004g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.155-15294A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988179 | ||||||
| chr4:17988214
|
G | C | 1 | a0001c0001t0001g0188 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.155-15329C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988214 | ||||||
| chr4:17988470
|
G | A | 38 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0002g0025others(35): Show | 38 | HG00438.hp2 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.155-15585C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988470 | ||||||
| chr4:17988526
|
T | C | 2 | a0001c0003t0003g0256a0001c0003t0003g0261 | 2 | HG02027.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.155-15641A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988526 | ||||||
| chr4:17988552
|
T | C | 6 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0222others(3): Show | 6 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-15667A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988552 | ||||||
| chr4:17988558
|
A | G | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-15673T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988558 | ||||||
| chr4:17988592
|
G | T | 1 | a0005c0006t0011g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.155-15707C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988592 | ||||||
| chr4:17988629
|
ATT | A | 78 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.155-15746_155-1574 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988629 | ||||||
| chr4:17988693
|
A | T | 1 | a0004c0005t0031g0284 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.155-15808T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988693 | ||||||
| chr4:17988712
|
C | T | 4 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0229others(1): Show | 4 | HG02145.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-15827G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988712 | ||||||
| chr4:17988750
|
C | G | 1 | a0001c0003t0003g0233 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.155-15865G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988750 | ||||||
| chr4:17988805
|
C | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-15920G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988805 | ||||||
| chr4:17988806
|
G | A | 1 | a0003c0004t0004g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.155-15921C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988806 | ||||||
| chr4:17988821
|
C | T | 11 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.155-15936G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988821 | ||||||
| chr4:17988941
|
G | A | 1 | a0002c0002t0035g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.155-16056C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17988941 | ||||||
| chr4:17989056
|
T | G | 1 | a0018c0021t0004g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.155-16171A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17989056 | ||||||
| chr4:17989167
|
C | T | 37 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(34): Show | 38 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.155-16282G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17989167 | ||||||
| chr4:17989301
|
G | T | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.155-16416C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17989301 | ||||||
| chr4:17989548
|
T | A | 1 | a0001c0003t0003g0254 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.155-16663A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17989548 | ||||||
| chr4:17989722
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.155-16837C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17989722 | ||||||
| chr4:17989800
|
C | T | 77 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(74): Show | 78 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.155-16915G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17989800 | ||||||
| chr4:17989899
|
A | C | 4 | a0001c0003t0001g0239a0001c0003t0003g0240a0001c0003t0025g0264others(1): Show | 5 | HG01074.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-17014T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17989899 | ||||||
| chr4:17990056
|
T | C | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.155-17171A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990056 | ||||||
| chr4:17990083
|
G | A | 5 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0223others(2): Show | 5 | HG02145.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-17198C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990083 | ||||||
| chr4:17990096
|
G | GT | 64 | a0001c0001t0001g0122a0001c0001t0001g0126a0001c0001t0001g0128others(61): Show | 64 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.155-17212dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990096 | ||||||
| chr4:17990096
|
G | GTT | 8 | a0001c0001t0001g0195a0001c0001t0002g0049a0001c0001t0017g0198others(5): Show | 8 | HG01069.hp1 HG01106.hp2 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.155-17213_155-1721 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990096 | ||||||
| chr4:17990096
|
GT | G | 16 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(13): Show | 16 | HG01891.hp1 HG02602.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.155-17212delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990096 | ||||||
| chr4:17990105
|
T | G | 15 | a0001c0003t0003g0214a0001c0003t0003g0216a0001c0003t0003g0238others(12): Show | 15 | HG00639.hp1 HG01192.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.155-17220A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990105 | ||||||
| chr4:17990115
|
T | C | 23 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224others(20): Show | 23 | HG00673.hp1 HG02602.hp2 HG02896.hp1 others(20): Show |
intron_variant | MODIFIER | c.155-17230A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990115 | ||||||
| chr4:17990143
|
G | T | 1 | a0004c0005t0031g0284 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.155-17258C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990143 | ||||||
| chr4:17990200
|
G | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.155-17315C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990200 | ||||||
| chr4:17990211
|
G | A | 1 | a0002c0002t0014g0211 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.155-17326C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990211 | ||||||
| chr4:17990383
|
GCC | G | 66 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(63): Show | 67 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.155-17500_155-1749 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990383 | ||||||
| chr4:17990391
|
G | A | 2 | a0001c0003t0003g0262a0001c0003t0003g0263 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.155-17506C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990391 | ||||||
| chr4:17990642
|
G | GT | 72 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(69): Show | 73 | HG00423.hp1 HG00639.hp1 HG00738.hp2 others(70): Show |
intron_variant | MODIFIER | c.155-17758dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990642 | ||||||
| chr4:17990642
|
G | GTT | 14 | a0001c0001t0006g0121a0002c0002t0020g0275a0002c0002t0020g0276others(11): Show | 14 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.155-17759_155-1775 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990642 | ||||||
| chr4:17990709
|
A | G | 79 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0228others(76): Show | 80 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.155-17824T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990709 | ||||||
| chr4:17990960
|
G | C | 1 | a0001c0003t0003g0257 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.155-18075C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17990960 | ||||||
| chr4:17991189
|
C | T | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.155-18304G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17991189 | ||||||
| chr4:17991280
|
T | G | 1 | a0001c0001t0001g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.155-18395A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17991280 | ||||||
| chr4:17991331
|
C | T | 1 | a0002c0002t0002g0069 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.155-18446G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17991331 | ||||||
| chr4:17991417
|
A | G | 11 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-18532T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17991417 | ||||||
| chr4:17991454
|
C | T | 4 | a0004c0024t0013g0088a0007c0008t0013g0217a0007c0008t0013g0218others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-18569G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17991454 | ||||||
| chr4:17991787
|
A | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(189): Show | 194 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.155-18902T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17991787 | ||||||
| chr4:17991890
|
CCTCACA | C | 55 | a0001c0001t0010g0228a0001c0001t0029g0232a0001c0003t0001g0239others(52): Show | 56 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.155-19011_155-1900 others(10): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17991890 | ||||||
| chr4:17991932
|
A | T | 1 | a0003c0004t0004g0110 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.155-19047T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17991932 | ||||||
| chr4:17991947
|
T | C | 11 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-19062A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17991947 | ||||||
| chr4:17992051
|
T | C | 1 | a0002c0002t0002g0048 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.155-19166A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17992051 | ||||||
| chr4:17992162
|
T | C | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.155-19277A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17992162 | ||||||
| chr4:17992434
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.155-19549G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17992434 | ||||||
| chr4:17992593
|
G | A | 1 | a0001c0001t0036g0075 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.155-19708C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17992593 | ||||||
| chr4:17992674
|
T | A | 1 | a0001c0001t0009g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.155-19789A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17992674 | ||||||
| chr4:17992675
|
T | C | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.155-19790A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17992675 | ||||||
| chr4:17992866
|
T | C | 1 | a0003c0004t0004g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.155-19981A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17992866 | ||||||
| chr4:17993038
|
C | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-20153G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993038 | ||||||
| chr4:17993296
|
G | A | 1 | a0002c0002t0002g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.155-20411C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993296 | ||||||
| chr4:17993424
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-20539A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993424 | ||||||
| chr4:17993501
|
G | A | 1 | a0001c0003t0003g0240 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.155-20616C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993501 | ||||||
| chr4:17993580
|
G | T | 11 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-20695C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993580 | ||||||
| chr4:17993589
|
A | T | 2 | a0014c0011t0004g0092a0014c0011t0004g0093 | 2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.155-20704T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993589 | ||||||
| chr4:17993615
|
A | T | 1 | a0001c0001t0001g0194 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.155-20730T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993615 | ||||||
| chr4:17993689
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-20804A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993689 | ||||||
| chr4:17993823
|
G | A | 1 | a0002c0002t0002g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.155-20938C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993823 | ||||||
| chr4:17993854
|
T | C | 1 | a0006c0007t0006g0274 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.155-20969A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993854 | ||||||
| chr4:17993877
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-20992A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17993877 | ||||||
| chr4:17994062
|
T | C | 1 | a0005c0006t0011g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.155-21177A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994062 | ||||||
| chr4:17994092
|
A | T | 3 | a0002c0002t0014g0211a0002c0002t0014g0212a0002c0002t0014g0213 | 3 | HG01891.hp2 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.155-21207T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994092 | ||||||
| chr4:17994189
|
A | G | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.155-21304T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994189 | ||||||
| chr4:17994328
|
G | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-21443C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994328 | ||||||
| chr4:17994370
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.155-21485G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994370 | ||||||
| chr4:17994423
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(76): Show | 80 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.155-21538T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994423 | ||||||
| chr4:17994585
|
C | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.155-21700G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994585 | ||||||
| chr4:17994729
|
G | GA | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-21845dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994729 | ||||||
| chr4:17994777
|
G | GA | 31 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(28): Show | 31 | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(28): Show |
intron_variant | MODIFIER | c.155-21893dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994777 | ||||||
| chr4:17994811
|
A | AT | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-21927dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994811 | ||||||
| chr4:17994824
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.155-21939T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994824 | ||||||
| chr4:17994844
|
T | TA | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-21960dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994844 | ||||||
| chr4:17994889
|
A | C | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.155-22004T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994889 | ||||||
| chr4:17994946
|
G | GA | 83 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(80): Show | 84 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.155-22062dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17994946 | ||||||
| chr4:17995205
|
AT | A | 54 | a0001c0003t0003g0214a0001c0003t0003g0215a0001c0003t0003g0216others(51): Show | 55 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.155-22321delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17995205 | ||||||
| chr4:17995205
|
ATT | A | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.155-22322_155-2232 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17995205 | ||||||
| chr4:17995299
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.155-22414T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17995299 | ||||||
| chr4:17995420
|
T | C | 2 | a0004c0005t0008g0280a0004c0005t0008g0281 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.155-22535A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17995420 | ||||||
| chr4:17995443
|
G | A | 80 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(77): Show | 81 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.155-22558C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17995443 | ||||||
| chr4:17995779
|
A | G | 6 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-22894T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17995779 | ||||||
| chr4:17995854
|
C | T | 1 | a0002c0002t0002g0041 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.155-22969G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17995854 | ||||||
| chr4:17995879
|
A | G | 1 | a0001c0003t0003g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.155-22994T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17995879 | ||||||
| chr4:17995918
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.155-23033A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17995918 | ||||||
| chr4:17996272
|
T | G | 4 | a0004c0024t0013g0088a0007c0008t0013g0217a0007c0008t0013g0218others(1): Show | 4 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-23387A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17996272 | ||||||
| chr4:17996420
|
C | T | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.155-23535G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17996420 | ||||||
| chr4:17996474
|
A | C | 1 | a0001c0003t0003g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.155-23589T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17996474 | ||||||
| chr4:17996709
|
T | A | 1 | a0003c0004t0004g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.155-23824A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17996709 | ||||||
| chr4:17996710
|
C | T | 1 | a0003c0004t0004g0098 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.155-23825G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17996710 | ||||||
| chr4:17996803
|
C | A | 70 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0002g0025others(67): Show | 70 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.155-23918G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17996803 | ||||||
| chr4:17996895
|
G | T | 1 | a0006c0007t0006g0272 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.155-24010C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17996895 | ||||||
| chr4:17997155
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.155-24270A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17997155 | ||||||
| chr4:17997219
|
A | G | 11 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-24334T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17997219 | ||||||
| chr4:17997346
|
G | A | 8 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(5): Show | 8 | HG01358.hp2 HG02451.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+24252C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17997346 | ||||||
| chr4:17997633
|
G | A | 2 | a0002c0002t0002g0076a0002c0002t0002g0077 | 2 | HG01123.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.154+23965C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17997633 | ||||||
| chr4:17997727
|
C | T | 1 | a0002c0002t0002g0037 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.154+23871G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17997727 | ||||||
| chr4:17997783
|
T | TTGAG | 83 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(80): Show | 84 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.154+23814_154+2381 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17997783 | ||||||
| chr4:17997844
|
A | G | 15 | a0001c0001t0002g0046a0001c0001t0002g0065a0002c0002t0002g0006others(12): Show | 15 | HG01074.hp2 HG01258.hp1 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.154+23754T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17997844 | ||||||
| chr4:17998466
|
T | C | 1 | a0001c0003t0003g0255 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.154+23132A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998466 | ||||||
| chr4:17998792
|
C | T | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+22806G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998792 | ||||||
| chr4:17998870
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+22728A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998870 | ||||||
| chr4:17998896
|
T | C | 2 | a0002c0002t0002g0022a0002c0002t0002g0023 | 2 | NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.154+22702A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998896 | ||||||
| chr4:17998964
|
C | CA | 9 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0193others(6): Show | 9 | HG02109.hp2 HG02602.hp2 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+22633dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998964 | ||||||
| chr4:17998964
|
C | CAAA | 8 | a0001c0001t0001g0130a0001c0001t0001g0191a0001c0001t0001g0192others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+22631_154+2263 others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998964 | ||||||
| chr4:17998964
|
C | CAAAAA | 14 | a0001c0001t0005g0114a0002c0002t0005g0113a0002c0002t0014g0212others(11): Show | 14 | HG00673.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.154+22629_154+2263 others(9): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998964 | ||||||
| chr4:17998964
|
C | CAAAAAA | 8 | a0002c0002t0005g0112a0002c0002t0005g0118a0002c0002t0005g0210others(5): Show | 8 | HG01243.hp1 HG02615.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+22628_154+2263 others(10): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998964 | ||||||
| chr4:17998975
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0003t0003g0240 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.154+22601_154+2262 others(26): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998975 | ||||||
| chr4:17998976
|
AAAAAAAA others(22): Show |
A | 1 | a0001c0003t0003g0244 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.154+22593_154+2262 others(33): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998976 | ||||||
| chr4:17998978
|
AAAAAAAA others(22): Show |
A | 26 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(23): Show | 27 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.154+22591_154+2261 others(33): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998978 | ||||||
| chr4:17998979
|
AAAAAAAA others(21): Show |
A | 2 | a0001c0003t0003g0256a0001c0003t0003g0257 | 2 | HG00423.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.154+22591_154+2261 others(32): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998979 | ||||||
| chr4:17998979
|
AAAAAAAA others(23): Show |
A | 3 | a0001c0003t0003g0236a0001c0003t0003g0237a0001c0003t0003g0258 | 3 | HG01243.hp2 HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.154+22589_154+2261 others(34): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998979 | ||||||
| chr4:17998980
|
AAAAAAAT others(20): Show |
A | 1 | a0005c0006t0011g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.154+22591_154+2261 others(31): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998980 | ||||||
| chr4:17998980
|
AAAAAAAT others(22): Show |
A | 7 | a0001c0003t0003g0260a0001c0003t0003g0261a0001c0003t0003g0267others(4): Show | 7 | HG01258.hp2 HG02027.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+22589_154+2261 others(33): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998980 | ||||||
| chr4:17998981
|
AAAAAATA others(19): Show |
A | 3 | a0005c0006t0011g0208a0005c0006t0011g0229a0005c0006t0011g0230 | 3 | HG02145.hp2 HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.154+22591_154+2261 others(30): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998981 | ||||||
| chr4:17998981
|
AAAAAATA others(23): Show |
A | 3 | a0001c0003t0003g0262a0001c0003t0003g0263a0001c0003t0022g0243 | 3 | HG02040.hp1 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.154+22587_154+2261 others(34): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998981 | ||||||
| chr4:17998982
|
AAAAATAT others(22): Show |
A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+22587_154+2261 others(33): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998982 | ||||||
| chr4:17998983
|
AAAATATA others(17): Show |
A | 1 | a0005c0006t0011g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.154+22591_154+2261 others(28): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998983 | ||||||
| chr4:17998983
|
AAAATATA others(19): Show |
A | 1 | a0005c0006t0005g0231 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.154+22589_154+2261 others(30): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998983 | ||||||
| chr4:17998984
|
AAATATAT others(20): Show |
A | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.154+22587_154+2261 others(31): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998984 | ||||||
| chr4:17998985
|
A | AAAAAAAA others(3): Show |
1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.154+22612_154+2261 others(14): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998985 | ||||||
| chr4:17998985
|
A | AAAT | 48 | a0001c0001t0001g0001a0001c0001t0001g0128a0001c0001t0001g0131others(45): Show | 49 | HG00438.hp1 HG01099.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.154+22612_154+2261 others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998985 | ||||||
| chr4:17998985
|
A | AAT | 7 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG01123.hp1 HG01169.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+22611_154+2261 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998985 | ||||||
| chr4:17998985
|
A | ATAT | 7 | a0001c0001t0001g0134a0001c0001t0001g0195a0001c0001t0009g0139others(4): Show | 7 | HG00423.hp2 HG01106.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+22612_154+2261 others(7): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998985 | ||||||
| chr4:17998985
|
A | T | 4 | a0002c0002t0005g0116a0002c0002t0005g0117a0003c0004t0004g0098others(1): Show | 4 | HG01081.hp2 HG02071.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+22613T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998985 | ||||||
| chr4:17998985
|
AATATATA others(19): Show |
A | 2 | a0004c0005t0008g0281a0004c0005t0008g0282 | 2 | HG02055.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.154+22587_154+2261 others(30): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998985 | ||||||
| chr4:17998985
|
AATATATA others(21): Show |
A | 5 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0029g0232others(2): Show | 5 | HG02615.hp1 HG02896.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+22585_154+2261 others(32): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998985 | ||||||
| chr4:17998986
|
AT | A | 14 | a0001c0001t0001g0068a0001c0001t0007g0014a0001c0001t0023g0007others(11): Show | 14 | HG01069.hp2 HG01081.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.154+22611delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998986 | ||||||
| chr4:17998986
|
ATATATAT others(4): Show |
A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.154+22601_154+2261 others(15): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998986 | ||||||
| chr4:17998986
|
ATATATAT others(18): Show |
A | 2 | a0004c0005t0008g0289a0004c0005t0031g0284 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.154+22587_154+2261 others(29): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998986 | ||||||
| chr4:17998986
|
ATATATAT others(20): Show |
A | 8 | a0001c0001t0010g0228a0004c0005t0008g0280a0004c0005t0008g0283others(5): Show | 8 | HG02145.hp1 HG02630.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+22585_154+2261 others(31): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998986 | ||||||
| chr4:17998986
|
ATATATAT others(22): Show |
A | 1 | a0001c0001t0040g0224 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.154+22583_154+2261 others(33): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998986 | ||||||
| chr4:17998987
|
T | A | 81 | a0001c0001t0001g0059a0001c0001t0002g0025a0001c0001t0002g0046others(78): Show | 81 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.154+22611A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998987 | ||||||
| chr4:17998989
|
T | A | 18 | a0001c0001t0005g0114a0002c0002t0002g0019a0002c0002t0002g0032others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.154+22609A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998989 | ||||||
| chr4:17998991
|
T | A | 9 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(6): Show | 9 | HG01109.hp2 HG01358.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.154+22607A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998991 | ||||||
| chr4:17998993
|
T | A | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+22605A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998993 | ||||||
| chr4:17998995
|
T | A | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG01891.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+22603A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998995 | ||||||
| chr4:17998997
|
T | A | 5 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0274others(2): Show | 5 | HG02451.hp1 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+22601A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998997 | ||||||
| chr4:17998999
|
T | A | 4 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0274others(1): Show | 4 | HG02976.hp2 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+22599A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998999 | ||||||
| chr4:17998999
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+22599A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17998999 | ||||||
| chr4:17999001
|
T | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.154+22597A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999001 | ||||||
| chr4:17999003
|
T | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.154+22595A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999003 | ||||||
| chr4:17999003
|
T | C | 5 | a0002c0002t0002g0022a0002c0002t0002g0023a0002c0002t0002g0028others(2): Show | 5 | HG06807.hp1 NA18943.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+22595A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999003 | ||||||
| chr4:17999005
|
C | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.154+22593G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999005 | ||||||
| chr4:17999005
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(111): Show | 115 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.154+22593G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999005 | ||||||
| chr4:17999007
|
C | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.154+22591G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999007 | ||||||
| chr4:17999007
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(99): Show | 103 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.154+22591G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999007 | ||||||
| chr4:17999009
|
C | A | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.154+22589G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999009 | ||||||
| chr4:17999009
|
C | CAT | 9 | a0002c0002t0002g0027a0002c0002t0002g0029a0002c0002t0002g0030others(6): Show | 9 | HG00735.hp2 HG00738.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.154+22587_154+2258 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999009 | ||||||
| chr4:17999009
|
C | T | 59 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0006g0120others(56): Show | 60 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.154+22589G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999009 | ||||||
| chr4:17999009
|
CAT | C | 8 | a0001c0001t0001g0068a0001c0001t0012g0082a0002c0002t0001g0085others(5): Show | 8 | HG00639.hp2 HG03017.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+22587_154+2258 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999009 | ||||||
| chr4:17999009
|
CATAT | C | 14 | a0001c0001t0001g0089a0001c0001t0001g0090a0003c0004t0004g0094others(11): Show | 14 | HG00673.hp1 HG03654.hp1 HG03927.hp1 others(11): Show |
intron_variant | MODIFIER | c.154+22585_154+2258 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999009 | ||||||
| chr4:17999009
|
CATATAT | C | 6 | a0003c0004t0002g0109a0003c0004t0004g0098a0003c0004t0004g0104others(3): Show | 6 | HG03490.hp1 HG03492.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+22583_154+2258 others(10): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999009 | ||||||
| chr4:17999011
|
T | C | 95 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(92): Show | 96 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.154+22587A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999011 | ||||||
| chr4:17999013
|
T | A | 4 | a0004c0005t0008g0281a0004c0005t0008g0282a0004c0005t0008g0289others(1): Show | 4 | HG02055.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+22585A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999013 | ||||||
| chr4:17999013
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0122a0001c0001t0001g0123others(89): Show | 93 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.154+22585A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999013 | ||||||
| chr4:17999015
|
T | A | 6 | a0001c0001t0010g0226a0001c0001t0021g0225a0004c0005t0008g0280others(3): Show | 6 | HG02055.hp2 HG02145.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.154+22583A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999015 | ||||||
| chr4:17999015
|
T | C | 18 | a0001c0001t0001g0193a0001c0001t0001g0194a0003c0004t0004g0094others(15): Show | 18 | HG00673.hp1 HG02109.hp2 HG02602.hp2 others(15): Show |
intron_variant | MODIFIER | c.154+22583A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999015 | ||||||
| chr4:17999017
|
T | C | 23 | a0001c0001t0001g0194a0003c0004t0002g0109a0003c0004t0004g0094others(20): Show | 23 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(20): Show |
intron_variant | MODIFIER | c.154+22581A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999017 | ||||||
| chr4:17999076
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+22522A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999076 | ||||||
| chr4:17999153
|
G | A | 2 | a0002c0002t0002g0072a0002c0002t0002g0079 | 2 | HG03834.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.154+22445C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999153 | ||||||
| chr4:17999170
|
C | T | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.154+22428G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999170 | ||||||
| chr4:17999191
|
A | AGCCGGGT others(12): Show |
288 | a0001c0001t0001g0001a0001c0001t0001g0059a0001c0001t0001g0068others(285): Show | 290 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(287): Show |
intron_variant | MODIFIER | c.154+22406_154+2240 others(23): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999191 | ||||||
| chr4:17999191
|
A | AGCCGGGT others(12): Show |
1 | a0001c0003t0003g0267 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.154+22406_154+2240 others(23): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999191 | ||||||
| chr4:17999270
|
G | A | 21 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(18): Show | 21 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+22328C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999270 | ||||||
| chr4:17999491
|
T | C | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.154+22107A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999491 | ||||||
| chr4:17999690
|
A | G | 1 | a0011c0028t0001g0137 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.154+21908T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999690 | ||||||
| chr4:17999874
|
G | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0207 | 3 | HG01433.hp2 HG01928.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.154+21724C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999874 | ||||||
| chr4:17999966
|
T | C | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154+21632A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 17999966 | ||||||
| chr4:18000065
|
G | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+21533C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18000065 | ||||||
| chr4:18000126
|
C | CT | 73 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0132others(70): Show | 73 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.154+21471dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18000126 | ||||||
| chr4:18000126
|
C | CTT | 26 | a0001c0001t0010g0228a0001c0001t0012g0082a0001c0001t0021g0225others(23): Show | 26 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.154+21470_154+2147 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18000126 | ||||||
| chr4:18000126
|
CT | C | 18 | a0001c0001t0001g0195a0001c0003t0003g0271a0001c0025t0026g0205others(15): Show | 18 | HG01099.hp2 HG01106.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.154+21471delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18000126 | ||||||
| chr4:18000395
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.154+21203C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18000395 | ||||||
| chr4:18000605
|
ATC | A | 70 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.154+20991_154+2099 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18000605 | ||||||
| chr4:18000835
|
T | C | 1 | a0020c0023t0002g0005 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.154+20763A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18000835 | ||||||
| chr4:18000844
|
T | A | 21 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(18): Show | 21 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+20754A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18000844 | ||||||
| chr4:18000960
|
C | T | 70 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.154+20638G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18000960 | ||||||
| chr4:18001138
|
TC | T | 3 | a0001c0001t0012g0082a0002c0002t0002g0083a0002c0002t0002g0084 | 3 | NA18981.hp2 NA19062.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.154+20459delG | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001138 | ||||||
| chr4:18001293
|
AATAG | A | 68 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(65): Show | 69 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.154+20301_154+2030 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001293 | ||||||
| chr4:18001377
|
T | C | 1 | a0001c0001t0007g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.154+20221A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001377 | ||||||
| chr4:18001427
|
T | C | 27 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(24): Show | 27 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.154+20171A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001427 | ||||||
| chr4:18001475
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.154+20123T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001475 | ||||||
| chr4:18001521
|
T | C | 1 | a0017c0017t0006g0273 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.154+20077A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001521 | ||||||
| chr4:18001735
|
T | A | 1 | a0001c0001t0001g0196 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.154+19863A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001735 | ||||||
| chr4:18001783
|
C | T | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.154+19815G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001783 | ||||||
| chr4:18001846
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.154+19752G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001846 | ||||||
| chr4:18001880
|
A | T | 1 | a0016c0029t0006g0285 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154+19718T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18001880 | ||||||
| chr4:18002034
|
T | A | 2 | a0003c0004t0004g0104a0003c0004t0004g0105 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.154+19564A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18002034 | ||||||
| chr4:18002095
|
G | A | 4 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0029g0232others(1): Show | 4 | HG02896.hp1 HG03453.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+19503C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18002095 | ||||||
| chr4:18002104
|
T | C | 5 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0274others(2): Show | 5 | HG02451.hp1 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+19494A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18002104 | ||||||
| chr4:18002189
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+19409A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18002189 | ||||||
| chr4:18002295
|
A | T | 7 | a0001c0003t0003g0233a0001c0003t0003g0234a0001c0003t0003g0241others(4): Show | 7 | HG00735.hp1 HG00738.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+19303T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18002295 | ||||||
| chr4:18002389
|
C | G | 1 | a0001c0001t0006g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.154+19209G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18002389 | ||||||
| chr4:18002391
|
G | A | 70 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.154+19207C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18002391 | ||||||
| chr4:18002467
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(85): Show | 89 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.154+19131A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18002467 | ||||||
| chr4:18003023
|
A | G | 6 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+18575T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003023 | ||||||
| chr4:18003094
|
T | G | 2 | a0004c0005t0008g0280a0004c0005t0008g0281 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.154+18504A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003094 | ||||||
| chr4:18003113
|
C | T | 3 | a0001c0001t0001g0132a0001c0001t0019g0133a0001c0001t0019g0204 | 3 | HG02717.hp1 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.154+18485G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003113 | ||||||
| chr4:18003132
|
A | G | 8 | a0004c0005t0008g0283a0004c0005t0008g0286a0004c0005t0008g0287others(5): Show | 8 | HG02145.hp1 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+18466T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003132 | ||||||
| chr4:18003151
|
G | C | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.154+18447C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003151 | ||||||
| chr4:18003353
|
T | C | 1 | a0008c0010t0001g0197 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.154+18245A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003353 | ||||||
| chr4:18003396
|
A | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+18202T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003396 | ||||||
| chr4:18003436
|
AT | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+18161delA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003436 | ||||||
| chr4:18003488
|
T | C | 3 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224 | 3 | HG02896.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154+18110A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003488 | ||||||
| chr4:18003500
|
A | G | 4 | a0001c0003t0001g0239a0001c0003t0003g0240a0001c0003t0025g0264others(1): Show | 5 | HG01074.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+18098T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003500 | ||||||
| chr4:18003627
|
C | A | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.154+17971G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003627 | ||||||
| chr4:18003742
|
G | A | 1 | a0001c0003t0025g0264 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.154+17856C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003742 | ||||||
| chr4:18003935
|
C | T | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154+17663G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003935 | ||||||
| chr4:18003985
|
C | T | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+17613G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18003985 | ||||||
| chr4:18004074
|
C | G | 6 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+17524G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004074 | ||||||
| chr4:18004102
|
A | G | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.154+17496T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004102 | ||||||
| chr4:18004170
|
C | A | 2 | a0001c0001t0017g0198a0001c0001t0017g0199 | 2 | HG02970.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.154+17428G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004170 | ||||||
| chr4:18004343
|
A | G | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+17255T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004343 | ||||||
| chr4:18004429
|
A | G | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+17169T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004429 | ||||||
| chr4:18004466
|
G | A | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.154+17132C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004466 | ||||||
| chr4:18004469
|
C | T | 1 | a0001c0003t0003g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.154+17129G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004469 | ||||||
| chr4:18004526
|
T | C | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.154+17072A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004526 | ||||||
| chr4:18004541
|
C | T | 1 | a0001c0003t0003g0238 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.154+17057G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004541 | ||||||
| chr4:18004636
|
T | C | 1 | a0003c0004t0004g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.154+16962A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004636 | ||||||
| chr4:18004867
|
G | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+16731C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004867 | ||||||
| chr4:18004904
|
G | A | 1 | a0001c0003t0003g0265 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.154+16694C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18004904 | ||||||
| chr4:18005032
|
C | T | 2 | a0001c0001t0002g0025a0002c0002t0002g0026 | 2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.154+16566G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18005032 | ||||||
| chr4:18005083
|
A | T | 1 | a0002c0002t0002g0024 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.154+16515T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18005083 | ||||||
| chr4:18005157
|
G | A | 1 | a0006c0007t0006g0278 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.154+16441C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18005157 | ||||||
| chr4:18005217
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+16381G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18005217 | ||||||
| chr4:18005328
|
C | T | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+16270G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18005328 | ||||||
| chr4:18005812
|
C | G | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+15786G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18005812 | ||||||
| chr4:18005933
|
C | T | 70 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.154+15665G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18005933 | ||||||
| chr4:18006138
|
A | C | 65 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0002g0025others(62): Show | 65 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.154+15460T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18006138 | ||||||
| chr4:18006246
|
C | G | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0207 | 3 | HG01433.hp2 HG01928.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.154+15352G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18006246 | ||||||
| chr4:18006511
|
G | A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+15087C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18006511 | ||||||
| chr4:18006576
|
A | C | 80 | a0001c0001t0006g0120a0001c0001t0006g0121a0001c0001t0010g0226others(77): Show | 81 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.154+15022T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18006576 | ||||||
| chr4:18006609
|
A | G | 203 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(200): Show | 205 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.154+14989T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18006609 | ||||||
| chr4:18006660
|
G | A | 3 | a0002c0002t0005g0116a0002c0002t0005g0117a0002c0026t0005g0115 | 3 | HG01081.hp2 HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154+14938C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18006660 | ||||||
| chr4:18006813
|
A | G | 1 | a0004c0005t0031g0284 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.154+14785T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18006813 | ||||||
| chr4:18007077
|
T | C | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.154+14521A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18007077 | ||||||
| chr4:18007353
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.154+14245G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18007353 | ||||||
| chr4:18007462
|
C | G | 1 | a0023c0016t0004g0091 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.154+14136G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18007462 | ||||||
| chr4:18007505
|
C | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+14093G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18007505 | ||||||
| chr4:18007808
|
A | G | 2 | a0001c0003t0003g0236a0001c0003t0003g0237 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.154+13790T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18007808 | ||||||
| chr4:18007865
|
A | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+13733T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18007865 | ||||||
| chr4:18008175
|
T | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+13423A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008175 | ||||||
| chr4:18008197
|
G | A | 1 | a0003c0004t0004g0107 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.154+13401C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008197 | ||||||
| chr4:18008336
|
G | A | 8 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(5): Show | 8 | HG01358.hp2 HG02451.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+13262C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008336 | ||||||
| chr4:18008362
|
T | A | 1 | a0001c0001t0001g0089 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.154+13236A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008362 | ||||||
| chr4:18008589
|
G | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+13009C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008589 | ||||||
| chr4:18008635
|
T | C | 8 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(5): Show | 8 | HG01358.hp2 HG02451.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+12963A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008635 | ||||||
| chr4:18008662
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.154+12936A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008662 | ||||||
| chr4:18008761
|
A | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(85): Show | 89 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.154+12837T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008761 | ||||||
| chr4:18008835
|
C | A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+12763G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008835 | ||||||
| chr4:18008851
|
T | G | 1 | a0001c0001t0001g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.154+12747A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18008851 | ||||||
| chr4:18009097
|
T | C | 3 | a0001c0001t0010g0226a0001c0001t0021g0225a0001c0001t0040g0224 | 3 | HG02896.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.154+12501A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009097 | ||||||
| chr4:18009293
|
T | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+12305A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009293 | ||||||
| chr4:18009324
|
T | C | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.154+12274A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009324 | ||||||
| chr4:18009337
|
G | A | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+12261C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009337 | ||||||
| chr4:18009382
|
T | A | 2 | a0002c0002t0005g0116a0002c0002t0005g0117 | 2 | HG01081.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.154+12216A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009382 | ||||||
| chr4:18009579
|
A | G | 70 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.154+12019T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009579 | ||||||
| chr4:18009609
|
G | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+11989C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009609 | ||||||
| chr4:18009638
|
C | G | 1 | a0003c0004t0004g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.154+11960G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009638 | ||||||
| chr4:18009813
|
G | A | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+11785C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009813 | ||||||
| chr4:18009943
|
C | T | 2 | a0004c0005t0008g0280a0004c0005t0008g0281 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.154+11655G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18009943 | ||||||
| chr4:18010113
|
C | A | 5 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 5 | HG01123.hp1 HG01943.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+11485G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010113 | ||||||
| chr4:18010237
|
TTTAC | T | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.154+11357_154+1136 others(8): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010237 | ||||||
| chr4:18010241
|
C | T | 27 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(24): Show | 27 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.154+11357G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010241 | ||||||
| chr4:18010312
|
T | C | 2 | a0003c0004t0002g0109a0003c0004t0004g0108 | 2 | NA18961.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.154+11286A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010312 | ||||||
| chr4:18010331
|
A | G | 1 | a0004c0005t0008g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154+11267T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010331 | ||||||
| chr4:18010396
|
G | GTC | 70 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.154+11200_154+1120 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010396 | ||||||
| chr4:18010412
|
G | A | 70 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.154+11186C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010412 | ||||||
| chr4:18010412
|
G | GTGTGTA | 6 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.154+11185_154+1118 others(10): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010412 | ||||||
| chr4:18010427
|
T | C | 1 | a0004c0005t0010g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.154+11171A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010427 | ||||||
| chr4:18010518
|
C | T | 1 | a0015c0015t0003g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.154+11080G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010518 | ||||||
| chr4:18010646
|
CTG | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+10950_154+1095 others(6): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010646 | ||||||
| chr4:18010649
|
T | A | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+10949A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010649 | ||||||
| chr4:18010650
|
A | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+10948T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010650 | ||||||
| chr4:18010722
|
G | A | 25 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(22): Show | 25 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.154+10876C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010722 | ||||||
| chr4:18010755
|
A | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+10843T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010755 | ||||||
| chr4:18010831
|
T | C | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+10767A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010831 | ||||||
| chr4:18010962
|
T | G | 1 | a0002c0002t0005g0118 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.154+10636A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010962 | ||||||
| chr4:18010973
|
A | G | 8 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(5): Show | 8 | HG01358.hp2 HG02451.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+10625T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18010973 | ||||||
| chr4:18011152
|
T | A | 8 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(5): Show | 8 | HG01358.hp2 HG02451.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+10446A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011152 | ||||||
| chr4:18011166
|
G | A | 2 | a0001c0001t0001g0202a0001c0001t0001g0203 | 2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.154+10432C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011166 | ||||||
| chr4:18011174
|
T | G | 2 | a0002c0002t0002g0078a0002c0002t0002g0079 | 2 | NA18964.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.154+10424A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011174 | ||||||
| chr4:18011217
|
T | C | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.154+10381A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011217 | ||||||
| chr4:18011364
|
G | A | 1 | a0001c0001t0010g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.154+10234C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011364 | ||||||
| chr4:18011429
|
T | A | 8 | a0001c0001t0019g0204a0002c0002t0020g0275a0002c0002t0020g0276others(5): Show | 8 | HG01358.hp2 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+10169A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011429 | ||||||
| chr4:18011430
|
A | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+10168T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011430 | ||||||
| chr4:18011516
|
C | T | 2 | a0002c0002t0002g0022a0002c0002t0002g0023 | 2 | NA19006.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.154+10082G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011516 | ||||||
| chr4:18011664
|
T | C | 19 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(16): Show | 19 | HG00673.hp1 HG02602.hp2 HG03017.hp1 others(16): Show |
intron_variant | MODIFIER | c.154+9934A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011664 | ||||||
| chr4:18011754
|
A | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+9844T>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011754 | ||||||
| chr4:18011793
|
C | T | 1 | a0001c0001t0009g0129 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.154+9805G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011793 | ||||||
| chr4:18011848
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+9750G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011848 | ||||||
| chr4:18011941
|
C | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+9657G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18011941 | ||||||
| chr4:18012001
|
C | G | 1 | a0001c0003t0003g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.154+9597G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18012001 | ||||||
| chr4:18012016
|
T | C | 43 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(40): Show | 44 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.154+9582A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18012016 | ||||||
| chr4:18012193
|
G | C | 4 | a0005c0006t0005g0231a0005c0006t0011g0208a0005c0006t0011g0229others(1): Show | 4 | HG02145.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+9405C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18012193 | ||||||
| chr4:18012529
|
C | G | 1 | a0001c0001t0007g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.154+9069G>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18012529 | ||||||
| chr4:18012545
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+9053G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18012545 | ||||||
| chr4:18012627
|
A | G | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+8971T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18012627 | ||||||
| chr4:18012679
|
G | GA | 11 | a0002c0002t0020g0275a0002c0002t0020g0276a0004c0024t0013g0088others(8): Show | 11 | HG01109.hp2 HG01243.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.154+8918dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18012679 | ||||||
| chr4:18013039
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+8559G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013039 | ||||||
| chr4:18013054
|
T | G | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+8544A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013054 | ||||||
| chr4:18013180
|
G | GT | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+8417dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013180 | ||||||
| chr4:18013533
|
T | A | 72 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0002g0025others(69): Show | 72 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.154+8065A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013533 | ||||||
| chr4:18013534
|
C | T | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+8064G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013534 | ||||||
| chr4:18013753
|
T | C | 1 | a0001c0001t0029g0232 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.154+7845A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013753 | ||||||
| chr4:18013761
|
G | C | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+7837C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013761 | ||||||
| chr4:18013817
|
A | AT | 88 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(85): Show | 89 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.154+7780dupA | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013817 | ||||||
| chr4:18013903
|
G | A | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+7695C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013903 | ||||||
| chr4:18013967
|
C | T | 3 | a0001c0003t0003g0233a0001c0003t0003g0234a0001c0003t0003g0270 | 3 | HG00738.hp2 HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.154+7631G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18013967 | ||||||
| chr4:18014495
|
T | A | 1 | a0002c0002t0002g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.154+7103A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18014495 | ||||||
| chr4:18014569
|
A | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+7029T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18014569 | ||||||
| chr4:18014706
|
T | A | 1 | a0001c0025t0026g0205 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.154+6892A>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18014706 | ||||||
| chr4:18014724
|
G | A | 1 | a0001c0003t0003g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.154+6874C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18014724 | ||||||
| chr4:18014739
|
C | A | 3 | a0007c0008t0013g0217a0007c0008t0013g0218a0007c0008t0013g0219 | 3 | HG01109.hp2 HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.154+6859G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18014739 | ||||||
| chr4:18014796
|
C | T | 1 | a0006c0007t0006g0272 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.154+6802G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18014796 | ||||||
| chr4:18015254
|
A | G | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+6344T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18015254 | ||||||
| chr4:18015568
|
T | C | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.154+6030A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18015568 | ||||||
| chr4:18015584
|
T | C | 2 | a0002c0002t0002g0080a0002c0002t0002g0081 | 2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.154+6014A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18015584 | ||||||
| chr4:18015694
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.154+5904G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18015694 | ||||||
| chr4:18015932
|
G | A | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+5666C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18015932 | ||||||
| chr4:18015980
|
T | C | 1 | a0003c0004t0004g0110 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.154+5618A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18015980 | ||||||
| chr4:18016107
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+5491A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016107 | ||||||
| chr4:18016177
|
C | CATA | 78 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(75): Show | 79 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.154+5418_154+5420d others(5): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016177 | ||||||
| chr4:18016315
|
A | T | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+5283T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016315 | ||||||
| chr4:18016488
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.154+5110T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016488 | ||||||
| chr4:18016602
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.154+4996A>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016602 | ||||||
| chr4:18016613
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+4985A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016613 | ||||||
| chr4:18016692
|
T | C | 2 | a0001c0001t0006g0120a0001c0001t0006g0121 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.154+4906A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016692 | ||||||
| chr4:18016706
|
C | T | 21 | a0003c0004t0002g0109a0003c0004t0004g0094a0003c0004t0004g0096others(18): Show | 21 | HG00673.hp1 HG02602.hp2 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+4892G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016706 | ||||||
| chr4:18016746
|
A | G | 1 | a0002c0002t0002g0009 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.154+4852T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016746 | ||||||
| chr4:18016817
|
G | T | 5 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 5 | HG01123.hp1 HG01943.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+4781C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016817 | ||||||
| chr4:18016848
|
C | A | 1 | a0001c0001t0001g0207 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.154+4750G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18016848 | ||||||
| chr4:18017240
|
T | C | 3 | a0001c0003t0003g0267a0001c0003t0003g0268a0001c0003t0003g0269 | 3 | HG02056.hp1 HG02129.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.154+4358A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18017240 | ||||||
| chr4:18017321
|
C | T | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+4277G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18017321 | ||||||
| chr4:18017402
|
T | C | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+4196A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18017402 | ||||||
| chr4:18017773
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.154+3825T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18017773 | ||||||
| chr4:18017790
|
C | T | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+3808G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18017790 | ||||||
| chr4:18017949
|
C | T | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+3649G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18017949 | ||||||
| chr4:18017965
|
T | C | 3 | a0001c0001t0012g0082a0002c0002t0002g0083a0002c0002t0002g0084 | 3 | NA18981.hp2 NA19062.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.154+3633A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18017965 | ||||||
| chr4:18018448
|
C | T | 2 | a0001c0001t0023g0007a0002c0002t0021g0008 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154+3150G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18018448 | ||||||
| chr4:18018533
|
G | A | 1 | a0002c0002t0001g0085 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.154+3065C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18018533 | ||||||
| chr4:18018622
|
C | A | 1 | a0002c0002t0002g0086 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.154+2976G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18018622 | ||||||
| chr4:18018635
|
G | C | 1 | a0002c0002t0002g0087 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.154+2963C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18018635 | ||||||
| chr4:18018925
|
G | T | 1 | a0002c0002t0002g0006 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.154+2673C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18018925 | ||||||
| chr4:18019199
|
C | T | 70 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.154+2399G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18019199 | ||||||
| chr4:18019529
|
C | T | 1 | a0004c0005t0004g0220 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.154+2069G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18019529 | ||||||
| chr4:18019684
|
C | T | 81 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(78): Show | 82 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.154+1914G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18019684 | ||||||
| chr4:18019687
|
G | GA | 90 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(87): Show | 91 | HG00423.hp2 HG00438.hp1 HG00642.hp2 others(88): Show |
intron_variant | MODIFIER | c.154+1910dupT | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18019687 | ||||||
| chr4:18019748
|
C | T | 70 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(67): Show | 71 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.154+1850G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18019748 | ||||||
| chr4:18020060
|
G | A | 26 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(23): Show | 26 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.154+1538C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020060 | ||||||
| chr4:18020147
|
C | A | 42 | a0001c0003t0001g0239a0001c0003t0003g0214a0001c0003t0003g0215others(39): Show | 43 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.154+1451G>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020147 | ||||||
| chr4:18020236
|
G | A | 1 | a0001c0003t0003g0271 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.154+1362C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020236 | ||||||
| chr4:18020273
|
G | C | 2 | a0002c0002t0005g0209a0002c0002t0005g0210 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.154+1325C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020273 | ||||||
| chr4:18020401
|
C | T | 1 | a0004c0005t0008g0282 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.154+1197G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020401 | ||||||
| chr4:18020515
|
A | T | 1 | a0020c0023t0002g0005 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.154+1083T>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020515 | ||||||
| chr4:18020572
|
A | G | 1 | a0001c0003t0003g0215 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.154+1026T>C | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020572 | ||||||
| chr4:18020750
|
G | T | 1 | a0002c0002t0002g0004 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.154+848C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020750 | ||||||
| chr4:18020756
|
A | ATG | 5 | a0001c0001t0001g0089a0001c0001t0001g0090a0004c0005t0008g0280others(2): Show | 5 | HG01358.hp2 HG02055.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+840_154+841dup others(2): Show |
LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020756 | ||||||
| chr4:18020839
|
G | C | 7 | a0002c0002t0020g0275a0002c0002t0020g0276a0006c0007t0006g0272others(4): Show | 7 | HG01358.hp2 HG02451.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+759C>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020839 | ||||||
| chr4:18020894
|
G | A | 3 | a0002c0002t0014g0211a0002c0002t0014g0212a0002c0002t0014g0213 | 3 | HG01891.hp2 HG02717.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.154+704C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18020894 | ||||||
| chr4:18021048
|
C | T | 1 | a0001c0003t0003g0214 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.154+550G>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18021048 | ||||||
| chr4:18021052
|
G | A | 1 | a0004c0020t0032g0279 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.154+546C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18021052 | ||||||
| chr4:18021069
|
T | C | 80 | a0001c0001t0010g0226a0001c0001t0010g0228a0001c0001t0021g0225others(77): Show | 81 | HG00423.hp1 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.154+529A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18021069 | ||||||
| chr4:18021123
|
G | A | 11 | a0004c0005t0008g0280a0004c0005t0008g0281a0004c0005t0008g0282others(8): Show | 11 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.154+475C>T | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18021123 | ||||||
| chr4:18021194
|
G | T | 1 | a0004c0024t0013g0088 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.154+404C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18021194 | ||||||
| chr4:18021211
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(203): Show | 208 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.154+387A>G | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18021211 | ||||||
| chr4:18021324
|
G | T | 1 | a0021c0018t0028g0003 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.154+274C>A | LCORL | ENSG00000178177.17 | transcript | ENST00000635767.2 | protein_coding | 1/7 | chr4 | 18021324 |