Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 3978 |
|---|---|
| ensemblid | ENSG00000105486.15 |
| hgncid | 6598 |
| symbol | LIG1 |
| name | DNA ligase 1 |
| refseq_nuc | NM_000234.3 |
| refseq_prot | NP_000225.1 |
| ensembl_nuc | ENST00000263274.12 |
| ensembl_prot | ENSP00000263274.6 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 48115445 |
| end | 48170344 |
| strand | - |
| ver | v1.2 |
| region | chr19:48115445-48170344 |
| region5000 | chr19:48110445-48175344 |
| regionname0 | LIG1_chr19_48115445_48170344 |
| regionname5000 | LIG1_chr19_48110445_48175344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001 | 1/1 | 919 | 310 | 78 | 56 | 130 | 9 | 35 | 97 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0002 | 0/0 | 919 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0003 | 0/0 | 919 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0004 | 0/0 | 919 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0005 | 0/0 | 919 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0006 | 0/0 | 919 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0007 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0008 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0009 | 0/0 | 919 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0010 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0011 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0012 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0013 | 0/0 | 919 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2760 | 117 | 23 | 20 | 59 | 6 | 8 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0002 | 0/0 | 2760 | 71 | 19 | 10 | 32 | 0 | 10 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0003 | 1/0 | 2760 | 69 | 13 | 20 | 22 | 1 | 12 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0004 | 0/0 | 2760 | 42 | 18 | 4 | 15 | 1 | 4 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0005 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0006 | 0/0 | 2760 | 4 | 3 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0007 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0008 | 0/0 | 2760 | 2 | 0 | 0 | 0 | 1 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0009 | 0/0 | 2760 | 2 | 0 | 0 | 2 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0010 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0011 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0012 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0013 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0014 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0015 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0016 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0017 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0018 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0019 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0020 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0021 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0022 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0023 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| c0024 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| 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 | 366 | 202 | 48 | 31 | 98 | 7 | 17 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| t0002 | 1/0 | 366 | 68 | 13 | 19 | 19 | 2 | 14 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| t0003 | 0/0 | 366 | 46 | 23 | 5 | 10 | 1 | 7 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| t0004 | 0/0 | 366 | 6 | 6 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| t0005 | 0/0 | 366 | 4 | 0 | 3 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| t0006 | 0/0 | 366 | 2 | 0 | 0 | 2 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| t0007 | 0/0 | 416 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| t0008 | 0/0 | 366 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| 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 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0309 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0013 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0001 | 0/1 | 2760 | 117 | 23 | 20 | 59 | 6 | 8 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0002 | 0/0 | 2760 | 71 | 19 | 10 | 32 | 0 | 10 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0003 | 1/0 | 2760 | 69 | 13 | 20 | 22 | 1 | 12 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0004 | 0/0 | 2760 | 42 | 18 | 4 | 15 | 1 | 4 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0007 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0009 | 0/0 | 2760 | 2 | 0 | 0 | 2 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0014 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0017 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0018 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0019 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0022 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0002c0005 | 0/0 | 2760 | 4 | 4 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0003c0006 | 0/0 | 2760 | 4 | 3 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0004c0008 | 0/0 | 2760 | 2 | 0 | 0 | 0 | 1 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0005c0011 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0006c0015 | 0/0 | 2760 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0007c0020 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0008c0012 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0009c0016 | 0/0 | 2760 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0010c0010 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0011c0021 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0012c0024 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0013c0023 | 0/0 | 2760 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0013t0007 | 0/0 | 3113 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0001t0001 | 0/1 | 3125 | 107 | 13 | 20 | 59 | 6 | 8 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0001t0003 | 0/0 | 3125 | 5 | 5 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0001t0004 | 0/0 | 3125 | 5 | 5 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0002t0001 | 0/0 | 3125 | 68 | 18 | 10 | 32 | 0 | 8 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0002t0003 | 0/0 | 3125 | 3 | 1 | 0 | 0 | 0 | 2 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0003t0002 | 1/0 | 3125 | 63 | 13 | 17 | 19 | 1 | 12 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0003t0005 | 0/0 | 3125 | 4 | 0 | 3 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0003t0006 | 0/0 | 3125 | 2 | 0 | 0 | 2 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0004t0001 | 0/0 | 3125 | 4 | 0 | 0 | 4 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0004t0003 | 0/0 | 3125 | 36 | 17 | 4 | 10 | 1 | 4 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0004t0004 | 0/0 | 3125 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0004t0008 | 0/0 | 3125 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0007t0001 | 0/0 | 3125 | 4 | 4 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0009t0001 | 0/0 | 3125 | 2 | 0 | 0 | 2 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0014t0003 | 0/0 | 3125 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0017t0002 | 0/0 | 3125 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0018t0001 | 0/0 | 3125 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0019t0002 | 0/0 | 3125 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0001c0022t0002 | 0/0 | 3125 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0002c0005t0001 | 0/0 | 3125 | 4 | 4 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0003c0006t0001 | 0/0 | 3125 | 4 | 3 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0004c0008t0001 | 0/0 | 3125 | 2 | 0 | 0 | 0 | 1 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0005c0011t0003 | 0/0 | 3125 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0006c0015t0002 | 0/0 | 3125 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0007c0020t0001 | 0/0 | 3125 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0008c0012t0001 | 0/0 | 3125 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0009c0016t0002 | 0/0 | 3125 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0010c0010t0001 | 0/0 | 3125 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0011c0021t0001 | 0/0 | 3125 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0012c0024t0001 | 0/0 | 3125 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| a0013c0023t0001 | 0/0 | 3125 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | copy fasta | chr19 | 48110445 | 48175344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0013t0007g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0309 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0002t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0059 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0003t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0004t0008g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0007t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0007t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0007t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0007t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0009t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0009t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0014t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0017t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0018t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0019t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0001c0022t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0002c0005t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0002c0005t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0002c0005t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0002c0005t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0003c0006t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0003c0006t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0003c0006t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0003c0006t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0004c0008t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0004c0008t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0005c0011t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0006c0015t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0007c0020t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0008c0012t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0009c0016t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0010c0010t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0011c0021t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0012c0024t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| a0013c0023t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0022 | t0002 | g0058 | EUR | GBR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | GBR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00140 | hp1 | a0001 | c0004 | t0003 | g0205 | EUR | GBR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00140 | hp2 | a0004 | c0008 | t0001 | g0268 | EUR | GBR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00621 | hp1 | a0001 | c0003 | t0002 | g0033 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0042 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00673 | hp1 | a0001 | c0004 | t0008 | g0328 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00673 | hp2 | a0001 | c0003 | t0002 | g0097 | EAS | CHS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00733 | hp1 | a0001 | c0003 | t0002 | g0083 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00733 | hp2 | a0003 | c0006 | t0001 | g0012 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0081 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0099 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00741 | hp1 | a0001 | c0003 | t0002 | g0024 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01071 | hp2 | a0001 | c0004 | t0003 | g0175 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01074 | hp1 | a0001 | c0003 | t0002 | g0065 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01109 | hp1 | a0001 | c0003 | t0005 | g0074 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01109 | hp2 | a0001 | c0004 | t0003 | g0195 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0060 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0158 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01175 | hp1 | a0001 | c0004 | t0003 | g0188 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01175 | hp2 | a0001 | c0003 | t0002 | g0092 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0093 | AMR | PUR | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01255 | hp2 | a0001 | c0003 | t0002 | g0071 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01257 | hp1 | a0001 | c0003 | t0002 | g0066 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0087 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01346 | hp2 | a0001 | c0003 | t0002 | g0061 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01358 | hp1 | a0001 | c0003 | t0002 | g0025 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0052 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0307 | EUR | IBS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0041 | EUR | IBS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0169 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01928 | hp1 | a0001 | c0003 | t0005 | g0075 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0110 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01934 | hp2 | a0001 | c0014 | t0003 | g0190 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0107 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02040 | hp2 | a0001 | c0004 | t0003 | g0212 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02056 | hp2 | a0001 | c0004 | t0003 | g0211 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02083 | hp1 | a0001 | c0004 | t0003 | g0191 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0023 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0067 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0035 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0080 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02155 | hp1 | a0001 | c0003 | t0002 | g0068 | EAS | CDX | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CDX | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02257 | hp2 | a0001 | c0004 | t0003 | g0197 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0325 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0078 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02273 | hp2 | a0001 | c0003 | t0005 | g0079 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02280 | hp2 | a0003 | c0006 | t0001 | g0010 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02293 | hp1 | a0001 | c0003 | t0002 | g0073 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02300 | hp2 | a0009 | c0016 | t0002 | g0027 | AMR | PEL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0072 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0172 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02523 | hp1 | a0008 | c0012 | t0001 | g0244 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02572 | hp1 | a0001 | c0004 | t0003 | g0204 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02572 | hp2 | a0002 | c0005 | t0001 | g0005 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0044 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02622 | hp1 | a0002 | c0005 | t0001 | g0007 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02622 | hp2 | a0001 | c0003 | t0002 | g0045 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02630 | hp1 | a0001 | c0004 | t0003 | g0176 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0053 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02647 | hp1 | a0001 | c0004 | t0003 | g0213 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0089 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02683 | hp1 | a0001 | c0003 | t0002 | g0098 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02683 | hp2 | a0004 | c0008 | t0001 | g0267 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02698 | hp1 | a0001 | c0003 | t0002 | g0063 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02717 | hp1 | a0001 | c0004 | t0003 | g0196 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0199 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02723 | hp1 | a0001 | c0007 | t0001 | g0136 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02723 | hp2 | a0002 | c0005 | t0001 | g0006 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02735 | hp1 | a0001 | c0017 | t0002 | g0055 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0076 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02738 | hp1 | a0001 | c0004 | t0003 | g0200 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02809 | hp1 | a0001 | c0004 | t0003 | g0208 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0100 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0324 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02886 | hp2 | a0001 | c0004 | t0003 | g0209 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02895 | hp2 | a0010 | c0010 | t0001 | g0085 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02896 | hp1 | a0001 | c0004 | t0003 | g0178 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0049 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0171 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02897 | hp2 | a0001 | c0003 | t0002 | g0048 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02965 | hp1 | a0001 | c0018 | t0001 | g0119 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02970 | hp1 | a0001 | c0004 | t0003 | g0186 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02976 | hp1 | a0001 | c0004 | t0003 | g0203 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02976 | hp2 | a0011 | c0021 | t0001 | g0103 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03017 | hp1 | a0006 | c0015 | t0002 | g0062 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03017 | hp2 | a0001 | c0004 | t0003 | g0185 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0170 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03098 | hp1 | a0013 | c0023 | t0001 | g0102 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03130 | hp1 | a0001 | c0004 | t0003 | g0181 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03130 | hp2 | a0003 | c0006 | t0001 | g0009 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03139 | hp2 | a0007 | c0020 | t0001 | g0151 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03195 | hp1 | a0001 | c0003 | t0002 | g0088 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03209 | hp2 | a0001 | c0004 | t0003 | g0216 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0173 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03453 | hp2 | a0001 | c0007 | t0001 | g0135 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03486 | hp1 | a0001 | c0003 | t0002 | g0054 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03490 | hp1 | a0001 | c0003 | t0002 | g0069 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0021 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03491 | hp2 | a0001 | c0004 | t0003 | g0193 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ESN | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0090 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0050 | AFR | GWD | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03669 | hp1 | a0001 | c0002 | t0003 | g0198 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0094 | SAS | PJL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | STU | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03688 | hp2 | a0001 | c0003 | t0002 | g0020 | SAS | STU | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03831 | hp1 | a0001 | c0003 | t0002 | g0082 | SAS | BEB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0043 | SAS | BEB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03834 | hp1 | a0005 | c0011 | t0003 | g0201 | SAS | BEB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | STU | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG04115 | hp2 | a0001 | c0003 | t0002 | g0026 | SAS | STU | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0022 | SAS | BEB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | BEB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | STU | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG04199 | hp2 | a0001 | c0004 | t0003 | g0215 | SAS | STU | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | STU | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0128 | SAS | STU | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18522 | hp1 | a0001 | c0004 | t0003 | g0002 | AFR | YRI | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | YRI | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | CHB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | CHB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0326 | AFR | YRI | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | YRI | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0056 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18944 | hp2 | a0001 | c0003 | t0006 | g0004 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18948 | hp2 | a0001 | c0009 | t0001 | g0126 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18950 | hp1 | a0001 | c0004 | t0003 | g0210 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0038 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18965 | hp1 | a0001 | c0004 | t0003 | g0179 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18966 | hp1 | a0001 | c0003 | t0002 | g0036 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18981 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18985 | hp1 | a0000 | c0013 | t0007 | g0182 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18989 | hp1 | a0001 | c0009 | t0001 | g0160 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18989 | hp2 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18990 | hp2 | a0001 | c0004 | t0001 | g0057 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18993 | hp1 | a0001 | c0003 | t0002 | g0040 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18994 | hp1 | a0001 | c0003 | t0002 | g0039 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18998 | hp2 | a0001 | c0004 | t0003 | g0214 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18999 | hp1 | a0001 | c0003 | t0006 | g0003 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19002 | hp2 | a0001 | c0004 | t0003 | g0184 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19007 | hp2 | a0001 | c0003 | t0002 | g0064 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19010 | hp1 | a0001 | c0003 | t0005 | g0077 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19012 | hp1 | a0001 | c0004 | t0003 | g0180 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19030 | hp1 | a0012 | c0024 | t0001 | g0101 | AFR | LWK | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19030 | hp2 | a0003 | c0006 | t0001 | g0011 | AFR | LWK | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0322 | AFR | LWK | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19043 | hp2 | a0001 | c0004 | t0004 | g0327 | AFR | LWK | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19057 | hp1 | a0001 | c0003 | t0002 | g0031 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19058 | hp2 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19066 | hp1 | a0001 | c0004 | t0003 | g0194 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19066 | hp2 | a0001 | c0003 | t0002 | g0034 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19068 | hp2 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0032 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0029 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19074 | hp1 | a0001 | c0003 | t0002 | g0030 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19085 | hp1 | a0001 | c0004 | t0003 | g0192 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | YRI | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA19240 | hp2 | a0001 | c0004 | t0003 | g0002 | AFR | YRI | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA20129 | hp1 | a0001 | c0007 | t0001 | g0162 | AFR | ASW | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ASW | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | TSI | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0218 | SAS | GIH | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | GIH | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01123 | hp1 | a0001 | c0019 | t0002 | g0084 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG01123 | hp2 | a0001 | c0004 | t0003 | g0187 | AMR | CLM | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0323 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02109 | hp2 | a0001 | c0004 | t0003 | g0189 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02486 | hp1 | a0002 | c0005 | t0001 | g0008 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | USA | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | USA | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18955 | hp1 | a0001 | c0004 | t0001 | g0096 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA20300 | hp1 | a0001 | c0004 | t0003 | g0206 | AFR | USA | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA20300 | hp2 | a0001 | c0007 | t0001 | g0137 | AFR | USA | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | LWK | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| NA21309 | hp2 | a0001 | c0004 | t0003 | g0174 | AFR | LWK | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0309 | REF | REF | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0059 | REF | REF | LIG1_chr19_48110445_48175344 | LIG1 | chr19 | 48110445 | 48175344 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48115647
|
GCTTAGTA others(56): Show |
G | 1 | a0000 | 1 | NA18985.hp1 | stop_lost&conservative_inframe_deletion | HIGH | c.2699_*1delAAAGTCAG others(55): Show |
p.Gln900_Ter920delin others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 2922/3125 | 2699/2760 | 900/919 | chr19 | 48115647 | ||
| chr19:48123268
|
G | T | 1 | a0009 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.2055C>A | p.Asn685Lys | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 22/28 | 2216/3125 | 2055/2760 | 685/919 | chr19 | 48123268 | ||
| chr19:48123283
|
C | G | 1 | a0008 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.2040G>C | p.Gln680His | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 22/28 | 2201/3125 | 2040/2760 | 680/919 | chr19 | 48123283 | ||
| chr19:48123293
|
C | A | 2 | a0012a0013 | 2 | HG03098.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.2030G>T | p.Arg677Leu | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 22/28 | 2191/3125 | 2030/2760 | 677/919 | chr19 | 48123293 | ||
| chr19:48127342
|
C | T | 1 | a0010 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.1939G>A | p.Asp647Asn | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/28 | 2100/3125 | 1939/2760 | 647/919 | chr19 | 48127342 | ||
| chr19:48128001
|
G | A | 1 | a0002 | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
missense_variant | MODERATE | c.1841C>T | p.Thr614Ile | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 20/28 | 2002/3125 | 1841/2760 | 614/919 | chr19 | 48128001 | ||
| chr19:48131087
|
G | A | 1 | a0007 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1810C>T | p.Arg604Cys | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/28 | 1971/3125 | 1810/2760 | 604/919 | chr19 | 48131087 | ||
| chr19:48131164
|
G | C | 1 | a0011 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1733C>G | p.Ala578Gly | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/28 | 1894/3125 | 1733/2760 | 578/919 | chr19 | 48131164 | ||
| chr19:48135765
|
T | C | 1 | a0002 | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
missense_variant | MODERATE | c.1438A>G | p.Met480Val | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/28 | 1599/3125 | 1438/2760 | 480/919 | chr19 | 48135765 | ||
| chr19:48136039
|
C | T | 1 | a0006 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1418G>A | p.Gly473Asp | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 15/28 | 1579/3125 | 1418/2760 | 473/919 | chr19 | 48136039 | ||
| chr19:48137068
|
A | G | 1 | a0013 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1271T>C | p.Ile424Thr | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/28 | 1432/3125 | 1271/2760 | 424/919 | chr19 | 48137068 | ||
| chr19:48137550
|
C | T | 1 | a0004 | 2 | HG00140.hp2 HG02683.hp2 |
missense_variant | MODERATE | c.1226G>A | p.Arg409His | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 13/28 | 1387/3125 | 1226/2760 | 409/919 | chr19 | 48137550 | ||
| chr19:48140013
|
C | T | 1 | a0005 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1045G>A | p.Val349Met | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/28 | 1206/3125 | 1045/2760 | 349/919 | chr19 | 48140013 | ||
| chr19:48143940
|
T | C | 1 | a0003 | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
missense_variant | MODERATE | c.800A>G | p.Asn267Ser | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 10/28 | 961/3125 | 800/2760 | 267/919 | chr19 | 48143940 | ||
| chr19:48162298
|
G | A | 2 | a0012a0013 | 2 | HG03098.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.71C>T | p.Ala24Val | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/28 | 232/3125 | 71/2760 | 24/919 | chr19 | 48162298 | ||
| chr19:48170243
|
T | C | 1 | a0001 | 6 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
splice_region_variant | LOW | c.-60A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/28 | chr19 | 48170243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48115709
|
T | C | 1 | a0003c0006 | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
synonymous_variant | LOW | c.2700A>G | p.Gln900Gln | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 2861/3125 | 2700/2760 | 900/919 | chr19 | 48115709 | ||
| chr19:48115897
|
C | T | 1 | a0001c0017 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.2652G>A | p.Pro884Pro | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 27/28 | 2813/3125 | 2652/2760 | 884/919 | chr19 | 48115897 | ||
| chr19:48117779
|
C | G | 12 | a0001c0001a0001c0002a0001c0009others(9): Show | 203 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(200): Show |
splice_region_variant&synonymous_variant | LOW | c.2442G>C | p.Ala814Ala | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/28 | 2603/3125 | 2442/2760 | 814/919 | chr19 | 48117779 | ||
| chr19:48119170
|
A | G | 18 | a0000c0013a0001c0001a0001c0002others(15): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
synonymous_variant | LOW | c.2406T>C | p.Asp802Asp | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/28 | 2567/3125 | 2406/2760 | 802/919 | chr19 | 48119170 | ||
| chr19:48121269
|
G | A | 1 | a0001c0018 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.2286C>T | p.Ile762Ile | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/28 | 2447/3125 | 2286/2760 | 762/919 | chr19 | 48121269 | ||
| chr19:48123310
|
T | C | 1 | a0001c0019 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.2013A>G | p.Val671Val | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 22/28 | 2174/3125 | 2013/2760 | 671/919 | chr19 | 48123310 | ||
| chr19:48136050
|
G | A | 1 | a0001c0014 | 1 | HG01934.hp2 | synonymous_variant | LOW | c.1407C>T | p.Leu469Leu | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 15/28 | 1568/3125 | 1407/2760 | 469/919 | chr19 | 48136050 | ||
| chr19:48136119
|
C | T | 1 | a0001c0009 | 2 | NA18948.hp2 NA18989.hp1 |
synonymous_variant | LOW | c.1338G>A | p.Leu446Leu | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 15/28 | 1499/3125 | 1338/2760 | 446/919 | chr19 | 48136119 | ||
| chr19:48137645
|
G | A | 1 | a0001c0022 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1131C>T | p.Gly377Gly | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 13/28 | 1292/3125 | 1131/2760 | 377/919 | chr19 | 48137645 | ||
| chr19:48151296
|
G | T | 12 | a0000c0013a0001c0001a0001c0004others(9): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
synonymous_variant | LOW | c.510C>A | p.Ala170Ala | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/28 | 671/3125 | 510/2760 | 170/919 | chr19 | 48151296 | ||
| chr19:48151299
|
C | T | 3 | a0010c0010a0012c0024a0013c0023 | 3 | HG02895.hp2 HG03098.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.507G>A | p.Val169Val | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/28 | 668/3125 | 507/2760 | 169/919 | chr19 | 48151299 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48115454
|
A | G | 24 | a0000c0013t0007a0001c0001t0001a0001c0001t0003others(21): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*195T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 195 | chr19 | 48115454 | |||||
| chr19:48115499
|
G | A | 1 | a0001c0003t0005 | 4 | HG01109.hp1 HG01928.hp1 HG02273.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*150C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 150 | chr19 | 48115499 | |||||
| chr19:48115540
|
C | G | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*109G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 109 | chr19 | 48115540 | |||||
| chr19:48115542
|
C | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*107G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 107 | chr19 | 48115542 | |||||
| chr19:48115543
|
A | ATATAAAG others(44): Show |
1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*105_*106insACACCT others(45): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 105 | chr19 | 48115543 | |||||
| chr19:48115548
|
C | G | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*101G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 101 | chr19 | 48115548 | |||||
| chr19:48115549
|
C | G | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 100 | chr19 | 48115549 | |||||
| chr19:48115553
|
G | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 96 | chr19 | 48115553 | |||||
| chr19:48115558
|
C | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 91 | chr19 | 48115558 | |||||
| chr19:48115559
|
C | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*90G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 90 | chr19 | 48115559 | |||||
| chr19:48115562
|
A | C | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 87 | chr19 | 48115562 | |||||
| chr19:48115563
|
G | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 86 | chr19 | 48115563 | |||||
| chr19:48115566
|
G | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*83C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 83 | chr19 | 48115566 | |||||
| chr19:48115570
|
T | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*79A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 79 | chr19 | 48115570 | |||||
| chr19:48115571
|
G | C | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*78C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 78 | chr19 | 48115571 | |||||
| chr19:48115572
|
C | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*77G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 77 | chr19 | 48115572 | |||||
| chr19:48115576
|
A | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*73T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 73 | chr19 | 48115576 | |||||
| chr19:48115580
|
C | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*69G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 69 | chr19 | 48115580 | |||||
| chr19:48115585
|
G | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*64C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 64 | chr19 | 48115585 | |||||
| chr19:48115586
|
C | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*63G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 63 | chr19 | 48115586 | |||||
| chr19:48115588
|
A | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*61T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 61 | chr19 | 48115588 | |||||
| chr19:48115589
|
T | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*60A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 60 | chr19 | 48115589 | |||||
| chr19:48115590
|
A | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 59 | chr19 | 48115590 | |||||
| chr19:48115594
|
A | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*55T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 55 | chr19 | 48115594 | |||||
| chr19:48115595
|
C | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 54 | chr19 | 48115595 | |||||
| chr19:48115596
|
C | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*53G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 53 | chr19 | 48115596 | |||||
| chr19:48115602
|
G | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*47C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 47 | chr19 | 48115602 | |||||
| chr19:48115604
|
C | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*45G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 45 | chr19 | 48115604 | |||||
| chr19:48115606
|
G | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 43 | chr19 | 48115606 | |||||
| chr19:48115610
|
A | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 39 | chr19 | 48115610 | |||||
| chr19:48115611
|
A | G | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 38 | chr19 | 48115611 | |||||
| chr19:48115618
|
C | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 31 | chr19 | 48115618 | |||||
| chr19:48115625
|
C | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 24 | chr19 | 48115625 | |||||
| chr19:48115626
|
C | G | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*23G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 23 | chr19 | 48115626 | |||||
| chr19:48115631
|
C | G | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*18G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 18 | chr19 | 48115631 | |||||
| chr19:48115632
|
C | G | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 17 | chr19 | 48115632 | |||||
| chr19:48115637
|
G | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 12 | chr19 | 48115637 | |||||
| chr19:48115643
|
G | T | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 6 | chr19 | 48115643 | |||||
| chr19:48115645
|
G | A | 1 | a0000c0013t0007 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 28/28 | 4 | chr19 | 48115645 | |||||
| chr19:48165573
|
G | A | 7 | a0000c0013t0007a0001c0001t0003a0001c0002t0003others(4): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-7C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/28 | chr19 | 48165573 | ||||||
| chr19:48170327
|
A | G | 1 | a0001c0003t0006 | 2 | NA18944.hp2 NA18999.hp1 |
5_prime_UTR_variant | MODIFIER | c.-144T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/28 | 4761 | chr19 | 48170327 | |||||
| chr19:48170333
|
G | A | 1 | a0001c0004t0008 | 1 | HG00673.hp1 | 5_prime_UTR_variant | MODIFIER | c.-150C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/28 | 4767 | chr19 | 48170333 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:48115798
|
C | G | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2677-66G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 27/27 | chr19 | 48115798 | ||||||
| chr19:48115847
|
C | A | 1 | a0001c0003t0002g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2676+26G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 27/27 | chr19 | 48115847 | ||||||
| chr19:48115970
|
G | A | 1 | a0001c0002t0001g0153 | 1 | HG02148.hp2 | splice_region_variant&intron_variant | LOW | c.2584-5C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48115970 | ||||||
| chr19:48116007
|
G | A | 1 | a0001c0003t0005g0077 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2584-42C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116007 | ||||||
| chr19:48116210
|
G | A | 1 | a0001c0004t0003g0181 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2584-245C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116210 | ||||||
| chr19:48116284
|
A | T | 1 | a0001c0003t0002g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2584-319T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116284 | ||||||
| chr19:48116303
|
A | G | 254 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(251): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.2584-338T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116303 | ||||||
| chr19:48116447
|
C | CA | 234 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(231): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.2584-483dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116447 | ||||||
| chr19:48116447
|
C | CAA | 15 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0001g0224others(12): Show | 15 | HG00597.hp2 HG02647.hp1 HG02738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2584-484_2584-483d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116447 | ||||||
| chr19:48116447
|
CA | C | 7 | a0001c0003t0002g0048a0001c0003t0002g0050a0001c0003t0002g0051others(4): Show | 7 | HG00733.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2584-483delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116447 | ||||||
| chr19:48116470
|
C | T | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2584-505G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116470 | ||||||
| chr19:48116529
|
G | A | 4 | a0001c0007t0001g0135a0001c0007t0001g0136a0001c0007t0001g0137others(1): Show | 4 | HG02723.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2584-564C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116529 | ||||||
| chr19:48116660
|
T | C | 1 | a0001c0003t0002g0045 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2584-695A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116660 | ||||||
| chr19:48116734
|
T | C | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2584-769A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116734 | ||||||
| chr19:48116759
|
TACAC | T | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2584-798_2584-795d others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116759 | ||||||
| chr19:48116916
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2583+722C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116916 | ||||||
| chr19:48116936
|
T | C | 1 | a0001c0004t0003g0189 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2583+702A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116936 | ||||||
| chr19:48116939
|
C | A | 43 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(40): Show | 44 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.2583+699G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48116939 | ||||||
| chr19:48117078
|
C | A | 1 | a0001c0001t0001g0303 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2583+560G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48117078 | ||||||
| chr19:48117112
|
G | A | 2 | a0001c0002t0001g0046a0001c0002t0001g0070 | 2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2583+526C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48117112 | ||||||
| chr19:48117246
|
G | A | 81 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(78): Show | 82 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.2583+392C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48117246 | ||||||
| chr19:48117411
|
C | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2583+227G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48117411 | ||||||
| chr19:48117491
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2583+147A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 26/27 | chr19 | 48117491 | ||||||
| chr19:48117965
|
G | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-184C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48117965 | ||||||
| chr19:48118036
|
T | A | 5 | a0001c0003t0002g0041a0001c0003t0002g0042a0001c0003t0002g0082others(2): Show | 5 | HG00099.hp1 HG00639.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2440-255A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118036 | ||||||
| chr19:48118078
|
G | A | 5 | a0001c0003t0002g0041a0001c0003t0002g0042a0001c0003t0002g0082others(2): Show | 5 | HG00099.hp1 HG00639.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.2440-297C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118078 | ||||||
| chr19:48118191
|
A | T | 1 | a0001c0002t0001g0110 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2440-410T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118191 | ||||||
| chr19:48118275
|
A | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2440-494T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118275 | ||||||
| chr19:48118290
|
G | A | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2440-509C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118290 | ||||||
| chr19:48118350
|
C | T | 3 | a0001c0003t0002g0054a0001c0003t0002g0089a0001c0003t0002g0090 | 3 | HG02647.hp2 HG03486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2440-569G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118350 | ||||||
| chr19:48118351
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2440-570C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118351 | ||||||
| chr19:48118431
|
T | C | 1 | a0001c0003t0002g0087 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2440-650A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118431 | ||||||
| chr19:48118534
|
C | CT | 87 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(84): Show | 88 | HG00558.hp2 HG00621.hp1 HG01167.hp1 others(85): Show |
intron_variant | MODIFIER | c.2439+602dupA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118534 | ||||||
| chr19:48118534
|
C | CTT | 8 | a0001c0002t0001g0018a0001c0002t0001g0113a0001c0002t0001g0144others(5): Show | 8 | HG00621.hp2 HG02148.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.2439+601_2439+602d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118534 | ||||||
| chr19:48118534
|
C | CTTT | 7 | a0001c0001t0001g0014a0001c0001t0001g0237a0001c0001t0001g0271others(4): Show | 7 | HG01070.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.2439+600_2439+602d others(5): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118534 | ||||||
| chr19:48118534
|
C | CTTTT | 90 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(87): Show | 90 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2439+599_2439+602d others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118534 | ||||||
| chr19:48118534
|
C | CTTTTT | 18 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0221others(15): Show | 18 | HG00597.hp2 HG01346.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.2439+598_2439+602d others(7): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118534 | ||||||
| chr19:48118562
|
A | G | 5 | a0001c0001t0001g0231a0001c0001t0001g0239a0001c0001t0001g0248others(2): Show | 5 | HG00741.hp2 HG01255.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2439+575T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118562 | ||||||
| chr19:48118597
|
G | A | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2439+540C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118597 | ||||||
| chr19:48118663
|
C | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439+474G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118663 | ||||||
| chr19:48118664
|
A | G | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439+473T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118664 | ||||||
| chr19:48118676
|
C | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439+461G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118676 | ||||||
| chr19:48118677
|
C | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439+460G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118677 | ||||||
| chr19:48118679
|
C | CAGGCATG others(128): Show |
5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439+457_2439+458i others(137): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118679 | ||||||
| chr19:48118687
|
C | A | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2439+450G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118687 | ||||||
| chr19:48118695
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2439+442G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118695 | ||||||
| chr19:48118700
|
G | A | 3 | a0001c0004t0003g0175a0001c0004t0003g0195a0001c0004t0003g0200 | 3 | HG01071.hp2 HG01109.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2439+437C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118700 | ||||||
| chr19:48118954
|
C | T | 52 | a0000c0013t0007g0182a0001c0002t0001g0168a0001c0002t0001g0169others(49): Show | 53 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.2439+183G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48118954 | ||||||
| chr19:48119085
|
C | T | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2439+52G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48119085 | ||||||
| chr19:48119096
|
G | A | 3 | a0001c0003t0002g0033a0001c0003t0002g0034a0001c0003t0002g0037 | 3 | HG00621.hp1 NA18981.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2439+41C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48119096 | ||||||
| chr19:48119118
|
C | T | 44 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.2439+19G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48119118 | ||||||
| chr19:48119125
|
G | A | 6 | a0001c0003t0002g0100a0003c0006t0001g0009a0003c0006t0001g0010others(3): Show | 6 | HG00733.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2439+12C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 25/27 | chr19 | 48119125 | ||||||
| chr19:48119226
|
A | G | 202 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(199): Show | 203 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.2386-36T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119226 | ||||||
| chr19:48119275
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2386-85A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119275 | ||||||
| chr19:48119288
|
A | G | 152 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(149): Show | 154 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(151): Show |
intron_variant | MODIFIER | c.2386-98T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119288 | ||||||
| chr19:48119294
|
G | A | 2 | a0001c0001t0001g0235a0001c0001t0001g0307 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2386-104C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119294 | ||||||
| chr19:48119299
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2386-109G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119299 | ||||||
| chr19:48119357
|
G | C | 1 | a0001c0001t0001g0311 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2386-167C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119357 | ||||||
| chr19:48119529
|
C | CT | 56 | a0000c0013t0007g0182a0001c0002t0001g0112a0001c0002t0001g0123others(53): Show | 57 | HG00140.hp1 HG00558.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.2386-340dupA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119529 | ||||||
| chr19:48119529
|
C | CTT | 11 | a0001c0004t0003g0181a0001c0004t0003g0194a0001c0004t0003g0197others(8): Show | 11 | HG02056.hp2 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2386-341_2386-340d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119529 | ||||||
| chr19:48119529
|
C | T | 1 | a0001c0003t0002g0034 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2386-339G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119529 | ||||||
| chr19:48119529
|
CT | C | 30 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(27): Show | 30 | HG00597.hp2 HG02056.hp1 HG02486.hp1 others(27): Show |
intron_variant | MODIFIER | c.2386-340delA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119529 | ||||||
| chr19:48119529
|
CTT | C | 96 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(93): Show | 96 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2386-341_2386-340d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119529 | ||||||
| chr19:48119529
|
CTTT | C | 13 | a0001c0001t0001g0222a0001c0001t0001g0226a0001c0001t0001g0237others(10): Show | 14 | HG00733.hp2 HG02132.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2386-342_2386-340d others(5): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119529 | ||||||
| chr19:48119688
|
A | G | 253 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(250): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.2386-498T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119688 | ||||||
| chr19:48119693
|
C | A | 1 | a0001c0002t0001g0125 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2386-503G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119693 | ||||||
| chr19:48119712
|
A | T | 1 | a0009c0016t0002g0027 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2386-522T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119712 | ||||||
| chr19:48119827
|
G | A | 1 | a0003c0006t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2386-637C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119827 | ||||||
| chr19:48119967
|
G | A | 26 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(23): Show | 26 | HG00673.hp1 HG01071.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.2386-777C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119967 | ||||||
| chr19:48119983
|
C | T | 5 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(2): Show | 5 | HG00733.hp2 HG02280.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2386-793G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48119983 | ||||||
| chr19:48120183
|
G | A | 66 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(63): Show | 67 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.2385+987C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48120183 | ||||||
| chr19:48120445
|
C | A | 1 | a0012c0024t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2385+725G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48120445 | ||||||
| chr19:48120456
|
G | A | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2385+714C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48120456 | ||||||
| chr19:48120629
|
T | C | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2385+541A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48120629 | ||||||
| chr19:48120691
|
G | A | 68 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(65): Show | 69 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.2385+479C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48120691 | ||||||
| chr19:48120696
|
C | G | 68 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(65): Show | 69 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.2385+474G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48120696 | ||||||
| chr19:48120699
|
C | T | 2 | a0001c0003t0002g0048a0001c0003t0002g0049 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2385+471G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48120699 | ||||||
| chr19:48120796
|
G | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2385+374C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48120796 | ||||||
| chr19:48121105
|
A | C | 1 | a0001c0003t0002g0037 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2385+65T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 24/27 | chr19 | 48121105 | ||||||
| chr19:48121337
|
G | A | 1 | a0013c0023t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2233-15C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121337 | ||||||
| chr19:48121368
|
C | T | 193 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.2233-46G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121368 | ||||||
| chr19:48121469
|
G | A | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2233-147C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121469 | ||||||
| chr19:48121521
|
G | T | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2233-199C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121521 | ||||||
| chr19:48121528
|
A | G | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2233-206T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121528 | ||||||
| chr19:48121568
|
G | A | 4 | a0001c0001t0004g0323a0001c0001t0004g0324a0001c0001t0004g0325others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2233-246C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121568 | ||||||
| chr19:48121573
|
G | A | 1 | a0001c0002t0001g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2233-251C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121573 | ||||||
| chr19:48121638
|
T | C | 201 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(198): Show | 202 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.2233-316A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121638 | ||||||
| chr19:48121658
|
G | A | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2233-336C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121658 | ||||||
| chr19:48121693
|
T | C | 201 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(198): Show | 202 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.2233-371A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121693 | ||||||
| chr19:48121879
|
G | A | 1 | a0001c0003t0002g0022 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2233-557C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121879 | ||||||
| chr19:48121879
|
G | T | 1 | a0001c0002t0001g0122 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2233-557C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121879 | ||||||
| chr19:48121955
|
G | A | 102 | a0001c0001t0001g0095a0001c0001t0001g0219a0001c0001t0001g0220others(99): Show | 102 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.2233-633C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48121955 | ||||||
| chr19:48122010
|
G | C | 3 | a0001c0004t0003g0002a0001c0004t0003g0196a0001c0004t0003g0197 | 4 | HG02257.hp2 HG02717.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2233-688C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122010 | ||||||
| chr19:48122170
|
C | T | 1 | a0001c0003t0002g0034 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2232+764G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122170 | ||||||
| chr19:48122219
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0227a0001c0001t0001g0228others(1): Show | 4 | NA18950.hp2 NA18973.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.2232+715C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122219 | ||||||
| chr19:48122249
|
G | A | 4 | a0001c0007t0001g0135a0001c0007t0001g0136a0001c0007t0001g0137others(1): Show | 4 | HG02723.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2232+685C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122249 | ||||||
| chr19:48122411
|
C | T | 1 | a0003c0006t0001g0011 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2232+523G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122411 | ||||||
| chr19:48122416
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2232+518G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122416 | ||||||
| chr19:48122535
|
G | A | 44 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.2232+399C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122535 | ||||||
| chr19:48122542
|
C | T | 1 | a0001c0003t0002g0089 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2232+392G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122542 | ||||||
| chr19:48122564
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2232+370C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122564 | ||||||
| chr19:48122749
|
C | T | 1 | a0001c0002t0001g0113 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2232+185G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122749 | ||||||
| chr19:48122860
|
C | T | 1 | a0008c0012t0001g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2232+74G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122860 | ||||||
| chr19:48122874
|
T | C | 8 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(5): Show | 8 | HG00733.hp2 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2232+60A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122874 | ||||||
| chr19:48122902
|
T | C | 8 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(5): Show | 8 | HG00733.hp2 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2232+32A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122902 | ||||||
| chr19:48122924
|
C | T | 8 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(5): Show | 8 | HG00733.hp2 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2232+10G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 23/27 | chr19 | 48122924 | ||||||
| chr19:48123101
|
G | A | 4 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2149+73C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 22/27 | chr19 | 48123101 | ||||||
| chr19:48123132
|
C | T | 6 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(3): Show | 6 | HG03098.hp2 HG03139.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2149+42G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 22/27 | chr19 | 48123132 | ||||||
| chr19:48123347
|
G | A | 79 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(76): Show | 80 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(77): Show |
intron_variant | MODIFIER | c.2005-29C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123347 | ||||||
| chr19:48123365
|
T | C | 1 | a0001c0003t0002g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2005-47A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123365 | ||||||
| chr19:48123375
|
A | T | 2 | a0001c0004t0003g0176a0001c0004t0003g0178 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2005-57T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123375 | ||||||
| chr19:48123475
|
C | T | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2005-157G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123475 | ||||||
| chr19:48123524
|
A | G | 1 | a0001c0004t0003g0184 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2005-206T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123524 | ||||||
| chr19:48123649
|
G | A | 1 | a0001c0003t0005g0075 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2005-331C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123649 | ||||||
| chr19:48123681
|
G | A | 107 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.2005-363C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123681 | ||||||
| chr19:48123789
|
C | T | 1 | a0001c0002t0001g0163 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2005-471G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123789 | ||||||
| chr19:48123836
|
C | T | 1 | a0003c0006t0001g0012 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2005-518G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123836 | ||||||
| chr19:48123852
|
A | AT | 184 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(181): Show | 185 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.2005-535dupA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123852 | ||||||
| chr19:48123854
|
T | TTA | 3 | a0001c0001t0001g0270a0001c0001t0001g0296a0001c0001t0004g0324 | 3 | HG02818.hp2 NA19083.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2005-537_2005-536i others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123854 | ||||||
| chr19:48123855
|
A | T | 65 | a0000c0013t0007g0182a0001c0001t0001g0134a0001c0001t0001g0284others(62): Show | 66 | HG00140.hp1 HG00673.hp1 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.2005-537T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123855 | ||||||
| chr19:48123856
|
A | T | 3 | a0001c0004t0003g0208a0012c0024t0001g0101a0013c0023t0001g0102 | 3 | HG02809.hp1 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2005-538T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123856 | ||||||
| chr19:48123920
|
C | T | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2005-602G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123920 | ||||||
| chr19:48123969
|
C | A | 1 | a0001c0001t0001g0272 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2005-651G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123969 | ||||||
| chr19:48123976
|
G | C | 1 | a0001c0001t0001g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2005-658C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48123976 | ||||||
| chr19:48124005
|
G | A | 254 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(251): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.2005-687C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124005 | ||||||
| chr19:48124364
|
C | T | 4 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2005-1046G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124364 | ||||||
| chr19:48124376
|
G | A | 1 | a0001c0002t0001g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2005-1058C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124376 | ||||||
| chr19:48124486
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2005-1168C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124486 | ||||||
| chr19:48124641
|
A | G | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2005-1323T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124641 | ||||||
| chr19:48124678
|
T | C | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2005-1360A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124678 | ||||||
| chr19:48124681
|
G | A | 1 | a0001c0003t0002g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2005-1363C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124681 | ||||||
| chr19:48124790
|
G | A | 11 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(8): Show | 11 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.2005-1472C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124790 | ||||||
| chr19:48124843
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2005-1525G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124843 | ||||||
| chr19:48124857
|
A | C | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2005-1539T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48124857 | ||||||
| chr19:48125010
|
C | CA | 9 | a0001c0001t0001g0221a0001c0001t0001g0243a0001c0001t0001g0282others(6): Show | 9 | HG01175.hp2 HG01433.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.2005-1693dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125010 | ||||||
| chr19:48125010
|
CA | C | 84 | a0001c0001t0001g0302a0001c0001t0003g0177a0001c0001t0003g0183others(81): Show | 85 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(82): Show |
intron_variant | MODIFIER | c.2005-1693delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125010 | ||||||
| chr19:48125052
|
A | C | 1 | a0001c0004t0003g0206 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2005-1734T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125052 | ||||||
| chr19:48125166
|
C | A | 3 | a0001c0004t0003g0002a0001c0004t0003g0196a0001c0004t0003g0197 | 4 | HG02257.hp2 HG02717.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2005-1848G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125166 | ||||||
| chr19:48125173
|
T | C | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2005-1855A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125173 | ||||||
| chr19:48125238
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2005-1920T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125238 | ||||||
| chr19:48125493
|
G | A | 1 | a0001c0004t0003g0212 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2004+1784C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125493 | ||||||
| chr19:48125501
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2004+1776C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125501 | ||||||
| chr19:48125504
|
GA | G | 68 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(65): Show | 69 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.2004+1772delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125504 | ||||||
| chr19:48125526
|
A | T | 44 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.2004+1751T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125526 | ||||||
| chr19:48125569
|
G | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+1708C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125569 | ||||||
| chr19:48125601
|
C | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+1676G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125601 | ||||||
| chr19:48125904
|
C | A | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2004+1373G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125904 | ||||||
| chr19:48125932
|
G | T | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+1345C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125932 | ||||||
| chr19:48125947
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2004+1330G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125947 | ||||||
| chr19:48125987
|
C | CA | 24 | a0001c0003t0002g0024a0001c0003t0002g0025a0001c0003t0002g0026others(21): Show | 24 | HG00099.hp1 HG00639.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.2004+1289dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125987 | ||||||
| chr19:48125987
|
CA | C | 228 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(225): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.2004+1289delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125987 | ||||||
| chr19:48125987
|
CAA | C | 12 | a0001c0001t0001g0269a0001c0001t0001g0285a0001c0001t0001g0298others(9): Show | 12 | HG01070.hp1 HG01891.hp1 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.2004+1288_2004+128 others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48125987 | ||||||
| chr19:48126030
|
G | A | 4 | a0001c0007t0001g0135a0001c0007t0001g0136a0001c0007t0001g0137others(1): Show | 4 | HG02723.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+1247C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126030 | ||||||
| chr19:48126115
|
T | C | 193 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(190): Show | 194 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.2004+1162A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126115 | ||||||
| chr19:48126121
|
A | C | 2 | a0001c0002t0001g0046a0001c0002t0001g0070 | 2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2004+1156T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126121 | ||||||
| chr19:48126536
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2004+741C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126536 | ||||||
| chr19:48126558
|
A | G | 2 | a0001c0002t0001g0117a0011c0021t0001g0103 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2004+719T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126558 | ||||||
| chr19:48126606
|
C | CA | 18 | a0001c0001t0001g0248a0001c0001t0001g0292a0001c0001t0001g0310others(15): Show | 18 | HG00733.hp2 HG01123.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2004+670dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126606 | ||||||
| chr19:48126606
|
CA | C | 7 | a0001c0001t0001g0229a0001c0001t0001g0303a0001c0002t0001g0106others(4): Show | 7 | HG02895.hp2 HG02897.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2004+670delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126606 | ||||||
| chr19:48126745
|
AT | A | 8 | a0001c0001t0001g0266a0001c0001t0001g0302a0001c0001t0004g0322others(5): Show | 8 | HG01517.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2004+531delA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126745 | ||||||
| chr19:48126761
|
T | G | 106 | a0001c0001t0001g0095a0001c0001t0001g0219a0001c0001t0001g0220others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2004+516A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126761 | ||||||
| chr19:48126783
|
T | C | 14 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(11): Show | 14 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2004+494A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126783 | ||||||
| chr19:48126934
|
G | A | 1 | a0001c0001t0001g0310 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2004+343C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126934 | ||||||
| chr19:48126987
|
T | C | 69 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(66): Show | 70 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.2004+290A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48126987 | ||||||
| chr19:48127037
|
A | AG | 43 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(40): Show | 44 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.2004+239dupC | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 21/27 | chr19 | 48127037 | ||||||
| chr19:48127443
|
GCC | G | 250 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(247): Show | 252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1933-97_1933-96del others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 20/27 | chr19 | 48127443 | ||||||
| chr19:48127506
|
G | C | 207 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 208 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1933-158C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 20/27 | chr19 | 48127506 | ||||||
| chr19:48127511
|
C | T | 1 | a0001c0003t0002g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1933-163G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 20/27 | chr19 | 48127511 | ||||||
| chr19:48127518
|
C | T | 43 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(40): Show | 44 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.1933-170G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 20/27 | chr19 | 48127518 | ||||||
| chr19:48127549
|
C | G | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1933-201G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 20/27 | chr19 | 48127549 | ||||||
| chr19:48127643
|
G | A | 2 | a0002c0005t0001g0005a0002c0005t0001g0006 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1932+267C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 20/27 | chr19 | 48127643 | ||||||
| chr19:48127874
|
C | G | 3 | a0001c0003t0002g0041a0001c0003t0002g0173a0001c0022t0002g0058 | 3 | HG00099.hp1 HG01517.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1932+36G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 20/27 | chr19 | 48127874 | ||||||
| chr19:48128060
|
G | A | 6 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822-40C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48128060 | ||||||
| chr19:48128071
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1822-51A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48128071 | ||||||
| chr19:48128151
|
C | T | 107 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.1822-131G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48128151 | ||||||
| chr19:48128312
|
G | A | 15 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(12): Show | 15 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1822-292C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48128312 | ||||||
| chr19:48128459
|
T | A | 1 | a0001c0002t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1822-439A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48128459 | ||||||
| chr19:48128580
|
G | A | 254 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(251): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1822-560C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48128580 | ||||||
| chr19:48128801
|
C | T | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1822-781G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48128801 | ||||||
| chr19:48128956
|
C | T | 6 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1822-936G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48128956 | ||||||
| chr19:48129015
|
C | T | 4 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1822-995G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129015 | ||||||
| chr19:48129042
|
G | C | 1 | a0001c0003t0002g0047 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1822-1022C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129042 | ||||||
| chr19:48129051
|
C | T | 7 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(4): Show | 7 | HG02109.hp1 HG02258.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.1822-1031G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129051 | ||||||
| chr19:48129075
|
GAC | G | 43 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(40): Show | 44 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.1822-1057_1822-105 others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129075 | ||||||
| chr19:48129112
|
G | A | 24 | a0001c0003t0002g0024a0001c0003t0002g0025a0001c0003t0002g0026others(21): Show | 24 | HG00099.hp1 HG00639.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1822-1092C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129112 | ||||||
| chr19:48129148
|
G | A | 6 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(3): Show | 6 | HG03098.hp2 HG03139.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1822-1128C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129148 | ||||||
| chr19:48129151
|
C | T | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1822-1131G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129151 | ||||||
| chr19:48129201
|
C | T | 81 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(78): Show | 82 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(79): Show |
intron_variant | MODIFIER | c.1822-1181G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129201 | ||||||
| chr19:48129343
|
G | A | 7 | a0001c0002t0001g0138a0001c0002t0001g0150a0001c0002t0001g0163others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1822-1323C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129343 | ||||||
| chr19:48129391
|
G | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1822-1371C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129391 | ||||||
| chr19:48129399
|
C | T | 1 | a0001c0002t0001g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1822-1379G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129399 | ||||||
| chr19:48129466
|
G | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1822-1446C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129466 | ||||||
| chr19:48129625
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1821+1451G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129625 | ||||||
| chr19:48129672
|
A | G | 1 | a0001c0002t0001g0156 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1821+1404T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129672 | ||||||
| chr19:48129709
|
A | G | 259 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(256): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1821+1367T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129709 | ||||||
| chr19:48129792
|
G | A | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1821+1284C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129792 | ||||||
| chr19:48129944
|
T | C | 259 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(256): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1821+1132A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48129944 | ||||||
| chr19:48130086
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1821+990T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130086 | ||||||
| chr19:48130186
|
G | GAAATTAC others(13): Show |
1 | a0001c0003t0002g0049 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1821+870_1821+889d others(22): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130186 | ||||||
| chr19:48130253
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | NA18948.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1821+823G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130253 | ||||||
| chr19:48130277
|
T | C | 206 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(203): Show | 207 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.1821+799A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130277 | ||||||
| chr19:48130321
|
G | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821+755C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130321 | ||||||
| chr19:48130387
|
G | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1821+689C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130387 | ||||||
| chr19:48130404
|
C | T | 5 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(2): Show | 5 | HG03098.hp2 HG03139.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1821+672G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130404 | ||||||
| chr19:48130432
|
C | T | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1821+644G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130432 | ||||||
| chr19:48130590
|
C | T | 68 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(65): Show | 69 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.1821+486G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130590 | ||||||
| chr19:48130907
|
T | C | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1821+169A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130907 | ||||||
| chr19:48130915
|
T | C | 2 | a0001c0001t0003g0183a0001c0001t0003g0217 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1821+161A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130915 | ||||||
| chr19:48130923
|
G | A | 1 | a0001c0003t0002g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1821+153C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48130923 | ||||||
| chr19:48131007
|
A | T | 6 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1821+69T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48131007 | ||||||
| chr19:48131041
|
C | T | 43 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(40): Show | 44 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.1821+35G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48131041 | ||||||
| chr19:48131059
|
G | C | 2 | a0002c0005t0001g0007a0002c0005t0001g0008 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1821+17C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48131059 | ||||||
| chr19:48131062
|
T | A | 207 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 208 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1821+14A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 19/27 | chr19 | 48131062 | ||||||
| chr19:48131302
|
A | G | 1 | a0001c0004t0003g0210 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1726-131T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131302 | ||||||
| chr19:48131393
|
C | A | 1 | a0001c0003t0002g0039 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1726-222G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131393 | ||||||
| chr19:48131411
|
A | G | 252 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(249): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1726-240T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131411 | ||||||
| chr19:48131424
|
CATGTGGG others(15): Show |
C | 1 | a0001c0002t0001g0146 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1726-275_1726-254d others(24): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131424 | ||||||
| chr19:48131534
|
A | C | 207 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 208 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1726-363T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131534 | ||||||
| chr19:48131570
|
C | T | 1 | a0001c0004t0003g0215 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1726-399G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131570 | ||||||
| chr19:48131703
|
T | C | 105 | a0001c0001t0001g0095a0001c0001t0001g0219a0001c0001t0001g0220others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1726-532A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131703 | ||||||
| chr19:48131788
|
C | T | 1 | a0001c0003t0002g0041 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1726-617G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131788 | ||||||
| chr19:48131790
|
G | GCATATAT others(19): Show |
1 | a0001c0004t0001g0086 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1726-645_1726-620d others(28): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131790 | ||||||
| chr19:48131934
|
CT | C | 209 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(206): Show | 211 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.1726-764delA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131934 | ||||||
| chr19:48131934
|
CTT | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0236a0001c0001t0001g0252others(6): Show | 9 | HG01070.hp2 HG01169.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1726-765_1726-764d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131934 | ||||||
| chr19:48131991
|
T | A | 4 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726-820A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48131991 | ||||||
| chr19:48132176
|
G | C | 208 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(205): Show | 209 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.1725+806C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132176 | ||||||
| chr19:48132327
|
C | A | 1 | a0001c0004t0003g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1725+655G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132327 | ||||||
| chr19:48132445
|
G | A | 43 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(40): Show | 44 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.1725+537C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132445 | ||||||
| chr19:48132645
|
G | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0315 | 3 | HG00597.hp2 HG00609.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1725+337C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132645 | ||||||
| chr19:48132648
|
G | A | 1 | a0001c0002t0001g0147 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1725+334C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132648 | ||||||
| chr19:48132653
|
C | T | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1725+329G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132653 | ||||||
| chr19:48132660
|
G | A | 6 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+322C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132660 | ||||||
| chr19:48132715
|
C | T | 207 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 208 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1725+267G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132715 | ||||||
| chr19:48132723
|
G | A | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1725+259C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132723 | ||||||
| chr19:48132790
|
C | CA | 49 | a0000c0013t0007g0182a0001c0003t0002g0020a0001c0003t0002g0024others(46): Show | 50 | HG00140.hp1 HG00673.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1725+191dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
C | CAA | 10 | a0001c0003t0002g0044a0001c0004t0003g0188a0001c0004t0003g0189others(7): Show | 10 | HG00673.hp1 HG01175.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1725+190_1725+191d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
C | CAAAAAA | 6 | a0001c0001t0003g0202a0001c0001t0003g0207a0001c0001t0003g0217others(3): Show | 6 | HG03098.hp2 HG03139.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1725+186_1725+191d others(8): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
C | CAAAAAAA | 8 | a0001c0001t0003g0183a0001c0001t0004g0322a0001c0002t0001g0107others(5): Show | 8 | HG01975.hp1 HG02717.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1725+185_1725+191d others(9): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
C | CAAAAAAA others(1): Show |
18 | a0001c0001t0003g0177a0001c0002t0001g0001a0001c0002t0001g0105others(15): Show | 19 | HG00621.hp2 HG01891.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.1725+184_1725+191d others(10): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
C | CAAAAAAA others(2): Show |
24 | a0001c0002t0001g0109a0001c0002t0001g0110a0001c0002t0001g0111others(21): Show | 24 | HG00558.hp2 HG01169.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.1725+183_1725+191d others(11): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
C | CAAAAAAA others(3): Show |
12 | a0001c0002t0001g0104a0001c0002t0001g0120a0001c0002t0001g0125others(9): Show | 12 | HG01167.hp1 HG01243.hp1 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.1725+182_1725+191d others(12): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
C | CAAAAAAA others(4): Show |
8 | a0001c0002t0001g0124a0001c0002t0001g0130a0001c0002t0001g0150others(5): Show | 8 | HG02145.hp2 HG02148.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1725+181_1725+191d others(13): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
C | CAAAAAAA others(5): Show |
4 | a0001c0002t0001g0043a0001c0002t0001g0091a0001c0002t0001g0117others(1): Show | 4 | HG01358.hp2 HG03516.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+180_1725+191d others(14): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
C | CAAAAAAA others(6): Show |
1 | a0001c0002t0001g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1725+179_1725+191d others(15): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
CA | C | 9 | a0001c0003t0002g0021a0001c0003t0002g0029a0001c0003t0002g0030others(6): Show | 9 | HG00140.hp2 HG02723.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.1725+191delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
CAA | C | 10 | a0001c0001t0001g0228a0001c0001t0001g0253a0001c0001t0001g0266others(7): Show | 10 | HG01928.hp2 HG02486.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.1725+190_1725+191d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
CAAA | C | 97 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 97 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1725+189_1725+191d others(5): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48132790
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0241a0001c0001t0001g0294 | 2 | HG02602.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1725+180_1725+191d others(14): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 18/27 | chr19 | 48132790 | ||||||
| chr19:48133277
|
T | G | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1610-180A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 17/27 | chr19 | 48133277 | ||||||
| chr19:48133401
|
A | C | 1 | a0001c0003t0002g0039 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1610-304T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 17/27 | chr19 | 48133401 | ||||||
| chr19:48133484
|
G | A | 78 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(75): Show | 79 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.1610-387C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 17/27 | chr19 | 48133484 | ||||||
| chr19:48133503
|
G | A | 80 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(77): Show | 81 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(78): Show |
intron_variant | MODIFIER | c.1610-406C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 17/27 | chr19 | 48133503 | ||||||
| chr19:48133752
|
C | T | 5 | a0001c0001t0001g0235a0001c0001t0001g0274a0001c0001t0001g0284others(2): Show | 5 | HG01074.hp2 HG01167.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1609+229G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 17/27 | chr19 | 48133752 | ||||||
| chr19:48133900
|
C | T | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609+81G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 17/27 | chr19 | 48133900 | ||||||
| chr19:48133925
|
G | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609+56C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 17/27 | chr19 | 48133925 | ||||||
| chr19:48134257
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG01981.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1524-191G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48134257 | ||||||
| chr19:48134328
|
G | T | 176 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1524-262C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48134328 | ||||||
| chr19:48134606
|
T | G | 68 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(65): Show | 69 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.1524-540A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48134606 | ||||||
| chr19:48135102
|
C | A | 207 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(204): Show | 208 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.1523+578G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135102 | ||||||
| chr19:48135147
|
G | A | 1 | a0001c0018t0001g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1523+533C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135147 | ||||||
| chr19:48135353
|
C | A | 1 | a0001c0001t0001g0295 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1523+327G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135353 | ||||||
| chr19:48135407
|
C | A | 4 | a0001c0007t0001g0135a0001c0007t0001g0136a0001c0007t0001g0137others(1): Show | 4 | HG02723.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523+273G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135407 | ||||||
| chr19:48135407
|
C | T | 3 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0172 | 3 | HG02451.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1523+273G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135407 | ||||||
| chr19:48135430
|
C | T | 68 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(65): Show | 69 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.1523+250G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135430 | ||||||
| chr19:48135452
|
G | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523+228C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135452 | ||||||
| chr19:48135457
|
C | T | 4 | a0001c0007t0001g0135a0001c0007t0001g0136a0001c0007t0001g0137others(1): Show | 4 | HG02723.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1523+223G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135457 | ||||||
| chr19:48135550
|
A | G | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1523+130T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135550 | ||||||
| chr19:48135560
|
C | A | 1 | a0001c0002t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1523+120G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135560 | ||||||
| chr19:48135638
|
G | C | 1 | a0001c0004t0003g0206 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1523+42C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135638 | ||||||
| chr19:48135668
|
C | T | 5 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(2): Show | 5 | HG03098.hp2 HG03139.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1523+12G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135668 | ||||||
| chr19:48135672
|
G | A | 1 | a0003c0006t0001g0012 | 1 | HG00733.hp2 | splice_region_variant&intron_variant | LOW | c.1523+8C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 16/27 | chr19 | 48135672 | ||||||
| chr19:48135904
|
C | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1424-125G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 15/27 | chr19 | 48135904 | ||||||
| chr19:48135904
|
C | T | 4 | a0001c0004t0003g0206a0001c0004t0003g0208a0001c0004t0003g0209others(1): Show | 4 | HG02809.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1424-125G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 15/27 | chr19 | 48135904 | ||||||
| chr19:48135978
|
G | A | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1423+56C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 15/27 | chr19 | 48135978 | ||||||
| chr19:48135984
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1423+50C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 15/27 | chr19 | 48135984 | ||||||
| chr19:48136215
|
T | C | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1332-90A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136215 | ||||||
| chr19:48136318
|
A | G | 1 | a0001c0003t0005g0075 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1332-193T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136318 | ||||||
| chr19:48136437
|
G | A | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1332-312C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136437 | ||||||
| chr19:48136464
|
A | G | 254 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(251): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1332-339T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136464 | ||||||
| chr19:48136601
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1331+407C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136601 | ||||||
| chr19:48136655
|
C | T | 78 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(75): Show | 79 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.1331+353G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136655 | ||||||
| chr19:48136725
|
G | A | 5 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(2): Show | 5 | HG03098.hp2 HG03139.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1331+283C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136725 | ||||||
| chr19:48136731
|
G | A | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331+277C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136731 | ||||||
| chr19:48136846
|
A | T | 4 | a0001c0001t0001g0231a0001c0001t0001g0239a0001c0001t0001g0254others(1): Show | 4 | HG00741.hp2 HG01255.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331+162T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136846 | ||||||
| chr19:48136974
|
C | A | 1 | a0001c0003t0002g0097 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1331+34G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136974 | ||||||
| chr19:48136977
|
C | G | 78 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(75): Show | 79 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.1331+31G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 14/27 | chr19 | 48136977 | ||||||
| chr19:48137106
|
C | T | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-22G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 13/27 | chr19 | 48137106 | ||||||
| chr19:48137173
|
G | C | 1 | a0001c0003t0002g0021 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1255-89C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 13/27 | chr19 | 48137173 | ||||||
| chr19:48137354
|
G | A | 1 | a0008c0012t0001g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1254+168C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 13/27 | chr19 | 48137354 | ||||||
| chr19:48137368
|
A | C | 254 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(251): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1254+154T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 13/27 | chr19 | 48137368 | ||||||
| chr19:48137380
|
AAGG | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0315 | 3 | HG00597.hp2 HG00609.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.1254+139_1254+141d others(5): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 13/27 | chr19 | 48137380 | ||||||
| chr19:48137483
|
G | C | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0255 | 3 | HG02132.hp2 NA18612.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1254+39C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 13/27 | chr19 | 48137483 | ||||||
| chr19:48137895
|
T | C | 1 | a0003c0006t0001g0012 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1088-207A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48137895 | ||||||
| chr19:48137916
|
GGTGGATG others(7): Show |
G | 1 | a0001c0002t0001g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1088-242_1088-229d others(16): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48137916 | ||||||
| chr19:48137961
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0296 | 2 | NA19083.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1088-273C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48137961 | ||||||
| chr19:48138062
|
C | T | 1 | a0001c0018t0001g0119 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1088-374G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138062 | ||||||
| chr19:48138205
|
G | C | 10 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1088-517C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138205 | ||||||
| chr19:48138249
|
T | A | 2 | a0002c0005t0001g0007a0002c0005t0001g0008 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1088-561A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138249 | ||||||
| chr19:48138317
|
A | G | 254 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(251): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1088-629T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138317 | ||||||
| chr19:48138424
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1088-736G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138424 | ||||||
| chr19:48138450
|
C | T | 3 | a0001c0004t0003g0175a0001c0004t0003g0195a0001c0004t0003g0200 | 3 | HG01071.hp2 HG01109.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1088-762G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138450 | ||||||
| chr19:48138512
|
C | G | 1 | a0001c0003t0002g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1088-824G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138512 | ||||||
| chr19:48138631
|
A | G | 4 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02970.hp2 HG03516.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1088-943T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138631 | ||||||
| chr19:48138640
|
G | A | 4 | a0001c0002t0001g0106a0001c0002t0001g0149a0001c0002t0001g0164others(1): Show | 4 | NA18973.hp1 NA18991.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-952C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138640 | ||||||
| chr19:48138758
|
A | G | 6 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088-1070T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138758 | ||||||
| chr19:48138767
|
GATCCTTC others(9): Show |
G | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1088-1095_1088-108 others(20): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138767 | ||||||
| chr19:48138780
|
C | G | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1088-1092G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48138780 | ||||||
| chr19:48139009
|
T | C | 201 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(198): Show | 202 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1087+962A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139009 | ||||||
| chr19:48139011
|
C | A | 90 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(87): Show | 91 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(88): Show |
intron_variant | MODIFIER | c.1087+960G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139011 | ||||||
| chr19:48139042
|
A | G | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+929T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139042 | ||||||
| chr19:48139069
|
C | A | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1087+902G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139069 | ||||||
| chr19:48139080
|
C | T | 43 | a0000c0013t0007g0182a0001c0004t0001g0032a0001c0004t0001g0057others(40): Show | 44 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.1087+891G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139080 | ||||||
| chr19:48139130
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1087+841C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139130 | ||||||
| chr19:48139234
|
G | A | 2 | a0012c0024t0001g0101a0013c0023t0001g0102 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1087+737C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139234 | ||||||
| chr19:48139274
|
C | T | 95 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(92): Show | 96 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(93): Show |
intron_variant | MODIFIER | c.1087+697G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139274 | ||||||
| chr19:48139497
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1087+474G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139497 | ||||||
| chr19:48139521
|
G | A | 1 | a0001c0002t0001g0167 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1087+450C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139521 | ||||||
| chr19:48139532
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1087+439C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139532 | ||||||
| chr19:48139554
|
G | C | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1087+417C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139554 | ||||||
| chr19:48139592
|
A | C | 1 | a0001c0004t0003g0194 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1087+379T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139592 | ||||||
| chr19:48139594
|
A | C | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1087+377T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139594 | ||||||
| chr19:48139595
|
C | A | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1087+376G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139595 | ||||||
| chr19:48139696
|
C | G | 2 | a0001c0004t0003g0195a0001c0004t0003g0200 | 2 | HG01109.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1087+275G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139696 | ||||||
| chr19:48139714
|
T | C | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1087+257A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139714 | ||||||
| chr19:48139750
|
T | C | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+221A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139750 | ||||||
| chr19:48139793
|
CCT | C | 111 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1087+176_1087+177d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139793 | ||||||
| chr19:48139867
|
T | C | 91 | a0001c0001t0003g0177a0001c0001t0003g0183a0001c0001t0003g0202others(88): Show | 92 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(89): Show |
intron_variant | MODIFIER | c.1087+104A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 12/27 | chr19 | 48139867 | ||||||
| chr19:48140343
|
C | T | 1 | a0001c0004t0003g0205 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.915-200G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140343 | ||||||
| chr19:48140425
|
T | C | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.915-282A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140425 | ||||||
| chr19:48140472
|
G | A | 1 | a0001c0002t0001g0114 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.915-329C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140472 | ||||||
| chr19:48140489
|
C | T | 2 | a0001c0004t0003g0195a0001c0004t0003g0200 | 2 | HG01109.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.915-346G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140489 | ||||||
| chr19:48140860
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.915-717G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140860 | ||||||
| chr19:48140892
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.915-749A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140892 | ||||||
| chr19:48140911
|
G | A | 2 | a0001c0002t0001g0109a0001c0002t0001g0152 | 2 | HG03490.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.915-768C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140911 | ||||||
| chr19:48140918
|
C | T | 1 | a0001c0004t0003g0215 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.915-775G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140918 | ||||||
| chr19:48140934
|
C | T | 112 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.915-791G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140934 | ||||||
| chr19:48140980
|
G | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG02523.hp2 NA19065.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.915-837C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48140980 | ||||||
| chr19:48141014
|
C | T | 14 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0269others(11): Show | 14 | HG00597.hp2 HG00609.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.915-871G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141014 | ||||||
| chr19:48141015
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG00735.hp1 HG00738.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.915-872C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141015 | ||||||
| chr19:48141017
|
A | G | 52 | a0000c0013t0007g0182a0001c0001t0004g0322a0001c0001t0004g0323others(49): Show | 52 | HG00140.hp1 HG00673.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.915-874T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141017 | ||||||
| chr19:48141291
|
G | A | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.915-1148C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141291 | ||||||
| chr19:48141296
|
A | T | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.915-1153T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141296 | ||||||
| chr19:48141369
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.915-1226A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141369 | ||||||
| chr19:48141378
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.915-1235G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141378 | ||||||
| chr19:48141384
|
G | A | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.915-1241C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141384 | ||||||
| chr19:48141407
|
C | CA | 48 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(45): Show | 49 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.915-1265dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141407 | ||||||
| chr19:48141481
|
G | A | 1 | a0001c0002t0001g0111 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.915-1338C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141481 | ||||||
| chr19:48141536
|
G | A | 1 | a0002c0005t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.915-1393C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141536 | ||||||
| chr19:48141621
|
A | T | 1 | a0001c0004t0001g0086 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.915-1478T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141621 | ||||||
| chr19:48141712
|
G | A | 4 | a0001c0007t0001g0135a0001c0007t0001g0136a0001c0007t0001g0137others(1): Show | 4 | HG02723.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.915-1569C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141712 | ||||||
| chr19:48141748
|
G | A | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.915-1605C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141748 | ||||||
| chr19:48141825
|
T | C | 2 | a0002c0005t0001g0007a0002c0005t0001g0008 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.915-1682A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141825 | ||||||
| chr19:48141842
|
C | A | 1 | a0001c0004t0003g0180 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.915-1699G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141842 | ||||||
| chr19:48141972
|
G | T | 248 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(245): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.914+1571C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48141972 | ||||||
| chr19:48142077
|
C | G | 252 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(249): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.914+1466G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142077 | ||||||
| chr19:48142117
|
C | G | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.914+1426G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142117 | ||||||
| chr19:48142127
|
C | A | 7 | a0001c0002t0001g0138a0001c0002t0001g0150a0001c0002t0001g0163others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.914+1416G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142127 | ||||||
| chr19:48142165
|
C | T | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.914+1378G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142165 | ||||||
| chr19:48142169
|
G | A | 1 | a0001c0002t0001g0123 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.914+1374C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142169 | ||||||
| chr19:48142254
|
A | G | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+1289T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142254 | ||||||
| chr19:48142271
|
A | G | 1 | a0008c0012t0001g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.914+1272T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142271 | ||||||
| chr19:48142287
|
C | A | 58 | a0001c0002t0001g0001a0001c0002t0001g0043a0001c0002t0001g0104others(55): Show | 59 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.914+1256G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142287 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(3): Show |
1 | a0002c0005t0001g0008 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.914+1091_914+1100d others(12): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(5): Show |
2 | a0012c0024t0001g0101a0013c0023t0001g0102 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.914+1089_914+1100d others(14): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(7): Show |
2 | a0001c0002t0001g0139a0011c0021t0001g0103 | 2 | HG02976.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.914+1087_914+1100d others(16): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(8): Show |
42 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(39): Show | 43 | HG00558.hp2 HG01167.hp1 HG01169.hp2 others(40): Show |
intron_variant | MODIFIER | c.914+1086_914+1100d others(17): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(9): Show |
23 | a0001c0001t0001g0302a0001c0002t0001g0091a0001c0002t0001g0106others(20): Show | 23 | HG00621.hp2 HG01358.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.914+1100_914+1101i others(18): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(10): Show |
6 | a0001c0001t0001g0281a0001c0001t0001g0291a0001c0002t0001g0019others(3): Show | 6 | HG00639.hp1 HG02148.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.914+1100_914+1101i others(19): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(11): Show |
40 | a0001c0001t0001g0095a0001c0001t0001g0221a0001c0001t0001g0222others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.914+1100_914+1101i others(20): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(12): Show |
41 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0224others(38): Show | 41 | HG00741.hp2 HG01070.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.914+1100_914+1101i others(21): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(13): Show |
15 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0228others(12): Show | 15 | HG00140.hp2 HG00423.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.914+1100_914+1101i others(22): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(14): Show |
6 | a0001c0001t0001g0232a0001c0001t0001g0276a0001c0001t0001g0294others(3): Show | 6 | HG00558.hp1 HG00597.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.914+1100_914+1101i others(23): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(15): Show |
5 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(2): Show | 5 | HG00735.hp1 HG00738.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.914+1100_914+1101i others(24): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0303a0002c0005t0001g0005 | 2 | HG02572.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.914+1100_914+1101i others(25): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
C | CAAAAAAA others(17): Show |
1 | a0002c0005t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.914+1100_914+1101i others(26): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142442
|
CA | C | 50 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(47): Show | 51 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(48): Show |
intron_variant | MODIFIER | c.914+1100delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142442 | ||||||
| chr19:48142444
|
A | AAAAAAAA others(12): Show |
3 | a0001c0001t0004g0325a0001c0001t0004g0326a0001c0007t0001g0135 | 3 | HG02258.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.914+1098_914+1099i others(21): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142444 | ||||||
| chr19:48142444
|
A | AAAAAAAA others(11): Show |
7 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(4): Show | 7 | HG02109.hp1 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.914+1098_914+1099i others(20): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142444 | ||||||
| chr19:48142445
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.914+1097_914+1098i others(20): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142445 | ||||||
| chr19:48142457
|
A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0266 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.914+1085_914+1086i others(20): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142457 | ||||||
| chr19:48142522
|
A | T | 1 | a0001c0003t0002g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.914+1021T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142522 | ||||||
| chr19:48142630
|
C | T | 9 | a0001c0001t0004g0322a0001c0001t0004g0324a0001c0001t0004g0325others(6): Show | 9 | HG02258.hp2 HG02723.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.914+913G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142630 | ||||||
| chr19:48142694
|
A | G | 200 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(197): Show | 201 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.914+849T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142694 | ||||||
| chr19:48142713
|
G | A | 196 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(193): Show | 197 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.914+830C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142713 | ||||||
| chr19:48142719
|
C | G | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.914+824G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142719 | ||||||
| chr19:48142755
|
T | C | 73 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0019others(70): Show | 74 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(71): Show |
intron_variant | MODIFIER | c.914+788A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142755 | ||||||
| chr19:48142761
|
A | C | 75 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0019others(72): Show | 76 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(73): Show |
intron_variant | MODIFIER | c.914+782T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142761 | ||||||
| chr19:48142776
|
C | T | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.914+767G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142776 | ||||||
| chr19:48142777
|
G | T | 1 | a0001c0001t0001g0302 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.914+766C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142777 | ||||||
| chr19:48142871
|
G | A | 1 | a0004c0008t0001g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.914+672C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48142871 | ||||||
| chr19:48143067
|
C | T | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.914+476G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48143067 | ||||||
| chr19:48143181
|
T | A | 1 | a0001c0001t0001g0302 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.914+362A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48143181 | ||||||
| chr19:48143325
|
C | T | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.914+218G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48143325 | ||||||
| chr19:48143385
|
C | T | 1 | a0001c0001t0004g0322 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.914+158G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48143385 | ||||||
| chr19:48143420
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0271 | 2 | NA19010.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.914+123G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48143420 | ||||||
| chr19:48143475
|
A | G | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.914+68T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48143475 | ||||||
| chr19:48143480
|
G | A | 3 | a0001c0002t0001g0146a0001c0002t0001g0147a0001c0002t0001g0148 | 3 | HG00621.hp2 NA18952.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.914+63C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48143480 | ||||||
| chr19:48143518
|
C | G | 4 | a0001c0002t0001g0046a0001c0002t0001g0070a0001c0002t0001g0113others(1): Show | 4 | HG03239.hp2 HG04184.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.914+25G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 11/27 | chr19 | 48143518 | ||||||
| chr19:48143626
|
T | C | 242 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(239): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.858-27A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 10/27 | chr19 | 48143626 | ||||||
| chr19:48143968
|
G | A | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.777-5C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48143968 | ||||||
| chr19:48143984
|
T | C | 48 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(45): Show | 49 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.777-21A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48143984 | ||||||
| chr19:48144160
|
T | A | 4 | a0001c0007t0001g0135a0001c0007t0001g0136a0001c0007t0001g0137others(1): Show | 4 | HG02723.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.777-197A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144160 | ||||||
| chr19:48144265
|
C | T | 2 | a0001c0001t0003g0183a0001c0001t0003g0217 | 2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.777-302G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144265 | ||||||
| chr19:48144355
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG00735.hp1 HG00738.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-392G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144355 | ||||||
| chr19:48144379
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.777-416T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144379 | ||||||
| chr19:48144397
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.777-434C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144397 | ||||||
| chr19:48144490
|
A | C | 252 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(249): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.777-527T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144490 | ||||||
| chr19:48144692
|
C | T | 4 | a0001c0002t0001g0120a0001c0002t0001g0121a0001c0002t0001g0122others(1): Show | 4 | HG02970.hp2 HG03516.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-729G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144692 | ||||||
| chr19:48144784
|
G | A | 2 | a0012c0024t0001g0101a0013c0023t0001g0102 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.777-821C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144784 | ||||||
| chr19:48144893
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.777-930G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144893 | ||||||
| chr19:48144894
|
G | A | 75 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0019others(72): Show | 76 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(73): Show |
intron_variant | MODIFIER | c.777-931C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144894 | ||||||
| chr19:48144969
|
T | C | 4 | a0001c0004t0003g0206a0001c0004t0003g0208a0001c0004t0003g0209others(1): Show | 4 | HG02809.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.777-1006A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144969 | ||||||
| chr19:48144980
|
G | A | 124 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(121): Show | 126 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(123): Show |
intron_variant | MODIFIER | c.777-1017C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48144980 | ||||||
| chr19:48145000
|
A | T | 252 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(249): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.777-1037T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145000 | ||||||
| chr19:48145066
|
C | T | 118 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.777-1103G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145066 | ||||||
| chr19:48145128
|
G | A | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.777-1165C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145128 | ||||||
| chr19:48145159
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777-1196T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145159 | ||||||
| chr19:48145174
|
T | C | 1 | a0001c0003t0002g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.777-1211A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145174 | ||||||
| chr19:48145212
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.777-1249G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145212 | ||||||
| chr19:48145213
|
G | C | 1 | a0001c0003t0002g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.777-1250C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145213 | ||||||
| chr19:48145214
|
T | C | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.777-1251A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145214 | ||||||
| chr19:48145246
|
G | A | 1 | a0001c0003t0002g0069 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.777-1283C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145246 | ||||||
| chr19:48145418
|
A | G | 1 | a0000c0013t0007g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.777-1455T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145418 | ||||||
| chr19:48145434
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.777-1471G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145434 | ||||||
| chr19:48145546
|
T | TGATGC | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 110 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.777-1588_777-1584d others(7): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145546 | ||||||
| chr19:48145581
|
T | C | 118 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.777-1618A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145581 | ||||||
| chr19:48145729
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.777-1766G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145729 | ||||||
| chr19:48145873
|
C | T | 48 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(45): Show | 49 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.777-1910G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145873 | ||||||
| chr19:48145922
|
A | G | 123 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.777-1959T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145922 | ||||||
| chr19:48145989
|
T | A | 1 | a0001c0017t0002g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.777-2026A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48145989 | ||||||
| chr19:48146026
|
C | G | 248 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(245): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.777-2063G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146026 | ||||||
| chr19:48146242
|
G | A | 8 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(5): Show | 8 | HG00733.hp2 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.777-2279C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146242 | ||||||
| chr19:48146441
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.777-2478T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146441 | ||||||
| chr19:48146537
|
G | A | 10 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.777-2574C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146537 | ||||||
| chr19:48146549
|
G | A | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.777-2586C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146549 | ||||||
| chr19:48146604
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.777-2641G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146604 | ||||||
| chr19:48146605
|
G | A | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.777-2642C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146605 | ||||||
| chr19:48146799
|
C | T | 1 | a0001c0002t0001g0153 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.777-2836G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146799 | ||||||
| chr19:48146978
|
G | C | 1 | a0001c0001t0001g0222 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.776+2785C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146978 | ||||||
| chr19:48146996
|
C | T | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.776+2767G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48146996 | ||||||
| chr19:48147066
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.776+2697G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147066 | ||||||
| chr19:48147067
|
G | A | 1 | a0001c0004t0003g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.776+2696C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147067 | ||||||
| chr19:48147105
|
T | C | 10 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.776+2658A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147105 | ||||||
| chr19:48147185
|
G | A | 1 | a0001c0003t0002g0042 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.776+2578C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147185 | ||||||
| chr19:48147474
|
C | T | 121 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(118): Show | 123 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.776+2289G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147474 | ||||||
| chr19:48147552
|
A | ACCACCTG others(4): Show |
1 | a0001c0002t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.776+2210_776+2211i others(13): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147552 | ||||||
| chr19:48147555
|
T | A | 1 | a0001c0002t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.776+2208A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147555 | ||||||
| chr19:48147563
|
C | G | 1 | a0001c0002t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.776+2200G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147563 | ||||||
| chr19:48147564
|
T | G | 1 | a0001c0002t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.776+2199A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147564 | ||||||
| chr19:48147568
|
G | C | 1 | a0001c0002t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.776+2195C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147568 | ||||||
| chr19:48147569
|
A | T | 1 | a0001c0002t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.776+2194T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147569 | ||||||
| chr19:48147645
|
TA | T | 242 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(239): Show | 244 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.776+2117delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147645 | ||||||
| chr19:48147680
|
CA | C | 48 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(45): Show | 49 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.776+2082delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147680 | ||||||
| chr19:48147708
|
T | C | 48 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(45): Show | 49 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.776+2055A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147708 | ||||||
| chr19:48147766
|
G | A | 2 | a0001c0002t0001g0091a0001c0018t0001g0119 | 2 | HG01358.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.776+1997C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147766 | ||||||
| chr19:48147777
|
T | C | 2 | a0001c0002t0001g0118a0001c0002t0001g0143 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.776+1986A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147777 | ||||||
| chr19:48147824
|
G | GA | 105 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.776+1938dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147824 | ||||||
| chr19:48147824
|
GA | G | 68 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0043others(65): Show | 69 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.776+1938delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147824 | ||||||
| chr19:48147933
|
C | A | 1 | a0001c0001t0001g0266 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.776+1830G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147933 | ||||||
| chr19:48147933
|
C | T | 111 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.776+1830G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48147933 | ||||||
| chr19:48148045
|
G | A | 130 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(127): Show | 132 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.776+1718C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148045 | ||||||
| chr19:48148064
|
A | AAGGGAG | 105 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.776+1693_776+1698d others(8): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148064 | ||||||
| chr19:48148127
|
C | A | 105 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.776+1636G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148127 | ||||||
| chr19:48148305
|
C | T | 4 | a0001c0007t0001g0135a0001c0007t0001g0136a0001c0007t0001g0137others(1): Show | 4 | HG02723.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.776+1458G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148305 | ||||||
| chr19:48148326
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.776+1437A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148326 | ||||||
| chr19:48148348
|
A | G | 130 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(127): Show | 132 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.776+1415T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148348 | ||||||
| chr19:48148371
|
A | G | 4 | a0003c0006t0001g0009a0003c0006t0001g0010a0003c0006t0001g0011others(1): Show | 4 | HG00733.hp2 HG02280.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.776+1392T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148371 | ||||||
| chr19:48148464
|
G | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.776+1299C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148464 | ||||||
| chr19:48148474
|
C | CA | 10 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0003t0002g0039others(7): Show | 10 | HG01109.hp1 HG01433.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.776+1288dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148474 | ||||||
| chr19:48148474
|
C | CAA | 6 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+1287_776+1288d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148474 | ||||||
| chr19:48148474
|
CA | C | 6 | a0001c0001t0001g0233a0001c0001t0001g0270a0001c0001t0001g0271others(3): Show | 6 | HG02895.hp2 HG03098.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.776+1288delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148474 | ||||||
| chr19:48148474
|
CAA | C | 82 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(79): Show | 83 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.776+1287_776+1288d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148474 | ||||||
| chr19:48148474
|
CAAA | C | 48 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(45): Show | 49 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.776+1286_776+1288d others(5): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148474 | ||||||
| chr19:48148630
|
G | A | 2 | a0001c0002t0001g0118a0001c0002t0001g0143 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.776+1133C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148630 | ||||||
| chr19:48148640
|
G | A | 1 | a0001c0003t0002g0022 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.776+1123C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148640 | ||||||
| chr19:48148708
|
C | G | 1 | a0001c0001t0001g0294 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.776+1055G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148708 | ||||||
| chr19:48148745
|
G | A | 130 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(127): Show | 132 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.776+1018C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148745 | ||||||
| chr19:48148812
|
T | C | 73 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0019others(70): Show | 74 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(71): Show |
intron_variant | MODIFIER | c.776+951A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148812 | ||||||
| chr19:48148888
|
C | A | 130 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(127): Show | 132 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.776+875G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148888 | ||||||
| chr19:48148983
|
C | T | 10 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.776+780G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48148983 | ||||||
| chr19:48149038
|
A | C | 121 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(118): Show | 123 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.776+725T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48149038 | ||||||
| chr19:48149127
|
C | T | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.776+636G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48149127 | ||||||
| chr19:48149257
|
A | T | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0305 | 3 | HG01346.hp1 HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.776+506T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48149257 | ||||||
| chr19:48149320
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.776+443G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48149320 | ||||||
| chr19:48149369
|
G | A | 121 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(118): Show | 123 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.776+394C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48149369 | ||||||
| chr19:48149543
|
G | A | 120 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(117): Show | 122 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.776+220C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48149543 | ||||||
| chr19:48149578
|
G | T | 48 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(45): Show | 49 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.776+185C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48149578 | ||||||
| chr19:48149616
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.776+147C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 9/27 | chr19 | 48149616 | ||||||
| chr19:48149928
|
T | C | 3 | a0001c0004t0003g0191a0001c0004t0003g0192a0001c0004t0008g0328 | 3 | HG00673.hp1 HG02083.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.698-87A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 8/27 | chr19 | 48149928 | ||||||
| chr19:48149953
|
G | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.698-112C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 8/27 | chr19 | 48149953 | ||||||
| chr19:48150039
|
C | A | 1 | a0001c0002t0001g0153 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.697+49G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 8/27 | chr19 | 48150039 | ||||||
| chr19:48150237
|
T | C | 1 | a0001c0002t0001g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.575-27A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/27 | chr19 | 48150237 | ||||||
| chr19:48150373
|
G | A | 1 | a0001c0003t0002g0060 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.575-163C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/27 | chr19 | 48150373 | ||||||
| chr19:48150396
|
C | A | 4 | a0001c0007t0001g0135a0001c0007t0001g0136a0001c0007t0001g0137others(1): Show | 4 | HG02723.hp1 HG03453.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-186G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/27 | chr19 | 48150396 | ||||||
| chr19:48150452
|
T | C | 1 | a0001c0001t0001g0315 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.575-242A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/27 | chr19 | 48150452 | ||||||
| chr19:48150543
|
G | A | 66 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0091others(63): Show | 67 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.575-333C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/27 | chr19 | 48150543 | ||||||
| chr19:48150654
|
T | C | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.575-444A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/27 | chr19 | 48150654 | ||||||
| chr19:48150957
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.574+275A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/27 | chr19 | 48150957 | ||||||
| chr19:48151114
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.574+118G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 7/27 | chr19 | 48151114 | ||||||
| chr19:48151356
|
C | T | 1 | a0001c0001t0001g0313 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.467-17G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151356 | ||||||
| chr19:48151393
|
G | A | 1 | a0001c0002t0001g0133 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.467-54C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151393 | ||||||
| chr19:48151455
|
G | A | 7 | a0001c0002t0001g0117a0001c0002t0001g0118a0001c0002t0001g0143others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.467-116C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151455 | ||||||
| chr19:48151459
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.467-120G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151459 | ||||||
| chr19:48151460
|
G | A | 1 | a0001c0003t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.467-121C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151460 | ||||||
| chr19:48151480
|
A | G | 15 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 15 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.467-141T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151480 | ||||||
| chr19:48151522
|
T | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 9 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.467-183A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151522 | ||||||
| chr19:48151630
|
C | T | 67 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0091others(64): Show | 68 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.467-291G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151630 | ||||||
| chr19:48151655
|
T | A | 1 | a0001c0001t0001g0282 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.467-316A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151655 | ||||||
| chr19:48151701
|
T | G | 15 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 15 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.467-362A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151701 | ||||||
| chr19:48151702
|
C | T | 15 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 15 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.467-363G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151702 | ||||||
| chr19:48151800
|
G | T | 1 | a0001c0003t0002g0061 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.467-461C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151800 | ||||||
| chr19:48151812
|
C | CCT | 176 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.467-474_467-473ins others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151812 | ||||||
| chr19:48151817
|
G | A | 2 | a0002c0005t0001g0005a0002c0005t0001g0006 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.467-478C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151817 | ||||||
| chr19:48151835
|
T | C | 2 | a0012c0024t0001g0101a0013c0023t0001g0102 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.467-496A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151835 | ||||||
| chr19:48151956
|
T | TA | 15 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(12): Show | 15 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.467-618dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151956 | ||||||
| chr19:48151966
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.467-627T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48151966 | ||||||
| chr19:48152192
|
G | A | 86 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 87 | HG00558.hp2 HG00621.hp2 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.467-853C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48152192 | ||||||
| chr19:48152205
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.467-866G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48152205 | ||||||
| chr19:48152295
|
A | G | 251 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(248): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.467-956T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48152295 | ||||||
| chr19:48152312
|
G | A | 3 | a0010c0010t0001g0085a0012c0024t0001g0101a0013c0023t0001g0102 | 3 | HG02895.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.467-973C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48152312 | ||||||
| chr19:48152502
|
T | C | 256 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(253): Show | 258 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.467-1163A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48152502 | ||||||
| chr19:48152615
|
G | A | 176 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.466+1257C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48152615 | ||||||
| chr19:48152816
|
G | T | 1 | a0001c0002t0001g0161 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.466+1056C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48152816 | ||||||
| chr19:48152923
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.466+949C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48152923 | ||||||
| chr19:48152943
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.466+929A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48152943 | ||||||
| chr19:48153077
|
C | T | 67 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0091others(64): Show | 68 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.466+795G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153077 | ||||||
| chr19:48153082
|
C | T | 1 | a0001c0004t0003g0215 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.466+790G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153082 | ||||||
| chr19:48153167
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.466+705G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153167 | ||||||
| chr19:48153192
|
C | CA | 37 | a0001c0001t0001g0234a0001c0001t0001g0241a0001c0001t0001g0252others(34): Show | 37 | HG00639.hp2 HG01891.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.466+679dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153192 | ||||||
| chr19:48153192
|
CA | C | 62 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(59): Show | 63 | HG00140.hp1 HG00673.hp1 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.466+679delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153192 | ||||||
| chr19:48153192
|
CAA | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+678_466+679del others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153192 | ||||||
| chr19:48153314
|
T | G | 160 | a0000c0013t0007g0182a0001c0001t0001g0095a0001c0001t0001g0134others(157): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.466+558A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153314 | ||||||
| chr19:48153367
|
T | C | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.466+505A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153367 | ||||||
| chr19:48153413
|
GA | G | 105 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.466+458delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153413 | ||||||
| chr19:48153536
|
C | T | 1 | a0001c0002t0001g0046 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.466+336G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153536 | ||||||
| chr19:48153622
|
C | A | 71 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0091others(68): Show | 72 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(69): Show |
intron_variant | MODIFIER | c.466+250G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153622 | ||||||
| chr19:48153625
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.466+247A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153625 | ||||||
| chr19:48153634
|
CA | C | 4 | a0001c0002t0001g0146a0001c0003t0002g0052a0001c0003t0002g0173others(1): Show | 4 | HG01433.hp2 HG03239.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+237delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153634 | ||||||
| chr19:48153635
|
AAAACACA others(3): Show |
A | 1 | a0000c0013t0007g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.466+227_466+236del others(10): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153635 | ||||||
| chr19:48153636
|
AAAC | A | 3 | a0001c0001t0004g0322a0001c0002t0001g0124a0001c0003t0002g0094 | 3 | HG03669.hp2 HG03688.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.466+233_466+235del others(3): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153636 | ||||||
| chr19:48153637
|
A | AAC | 26 | a0001c0001t0001g0221a0001c0001t0001g0235a0001c0001t0001g0236others(23): Show | 26 | HG00597.hp2 HG00735.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.466+233_466+234dup others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
A | AACAC | 11 | a0001c0001t0001g0234a0001c0001t0001g0254a0001c0001t0001g0266others(8): Show | 11 | HG00673.hp2 HG01070.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.466+231_466+234dup others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
A | AACACAC | 4 | a0001c0001t0001g0231a0001c0001t0001g0265a0001c0003t0002g0025others(1): Show | 4 | HG01255.hp1 HG01358.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+229_466+234dup others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
A | C | 1 | a0001c0003t0002g0078 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.466+235T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AAC | A | 63 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0225others(60): Show | 63 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.466+233_466+234del others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACAC | A | 65 | a0001c0001t0001g0227a0001c0001t0001g0237a0001c0001t0001g0238others(62): Show | 66 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.466+231_466+234del others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACACAC | A | 41 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0283others(38): Show | 41 | HG00140.hp2 HG00558.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.466+229_466+234del others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACACACA others(1): Show |
A | 32 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(29): Show | 33 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.466+227_466+234del others(8): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACACACA others(3): Show |
A | 10 | a0001c0002t0001g0156a0001c0003t0002g0056a0001c0004t0001g0032others(7): Show | 10 | HG00673.hp1 HG00733.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.466+225_466+234del others(10): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACACACA others(5): Show |
A | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0004t0003g0193 | 3 | HG01070.hp2 HG01071.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.466+223_466+234del others(12): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACACACA others(7): Show |
A | 2 | a0001c0004t0001g0057a0002c0005t0001g0008 | 2 | HG02486.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.466+221_466+234del others(14): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACACACA others(9): Show |
A | 3 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007 | 3 | HG02572.hp2 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.466+219_466+234del others(16): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACACACA others(11): Show |
A | 1 | a0001c0003t0002g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.466+217_466+234del others(18): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACACACA others(13): Show |
A | 1 | a0001c0002t0001g0147 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.466+215_466+234del others(20): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153637
|
AACACACA others(17): Show |
A | 3 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0172 | 3 | HG02451.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.466+211_466+234del others(24): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153637 | ||||||
| chr19:48153690
|
A | C | 2 | a0001c0002t0001g0118a0001c0002t0001g0143 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.466+182T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153690 | ||||||
| chr19:48153738
|
T | TCA | 97 | a0001c0001t0001g0242a0001c0001t0001g0260a0001c0001t0001g0273others(94): Show | 98 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.466+132_466+133dup others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153738 | ||||||
| chr19:48153738
|
T | TCACA | 23 | a0001c0001t0001g0261a0001c0001t0003g0217a0001c0003t0002g0022others(20): Show | 23 | HG00140.hp1 HG00673.hp1 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.466+130_466+133dup others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153738 | ||||||
| chr19:48153738
|
T | TCACACA | 8 | a0000c0013t0007g0182a0001c0003t0002g0047a0001c0003t0002g0097others(5): Show | 8 | HG00673.hp2 HG01123.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+128_466+133dup others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153738 | ||||||
| chr19:48153738
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0001g0225a0001c0001t0001g0227a0013c0023t0001g0102 | 3 | HG03098.hp1 NA18973.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.466+124_466+133dup others(10): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153738 | ||||||
| chr19:48153738
|
T | TCACACAC others(5): Show |
2 | a0001c0001t0001g0228a0012c0024t0001g0101 | 2 | NA18950.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.466+122_466+133dup others(12): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153738 | ||||||
| chr19:48153738
|
TCA | T | 10 | a0001c0001t0001g0264a0001c0003t0002g0076a0001c0003t0002g0083others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.466+132_466+133del others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153738 | ||||||
| chr19:48153738
|
TCACA | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(4): Show | 7 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.466+130_466+133del others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153738 | ||||||
| chr19:48153738
|
TCACACA | T | 4 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0002t0001g0123others(1): Show | 4 | HG02895.hp2 NA18948.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+128_466+133del others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153738 | ||||||
| chr19:48153772
|
A | ACACACC | 11 | a0001c0002t0001g0018a0001c0002t0001g0120a0001c0002t0001g0121others(8): Show | 11 | HG00099.hp1 HG02717.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.466+99_466+100insG others(5): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153772 | ||||||
| chr19:48153772
|
A | ACACC | 40 | a0001c0002t0001g0104a0001c0002t0001g0106a0001c0002t0001g0107others(37): Show | 40 | HG00558.hp2 HG01934.hp1 HG01952.hp1 others(37): Show |
intron_variant | MODIFIER | c.466+99_466+100insG others(3): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153772 | ||||||
| chr19:48153772
|
A | C | 14 | a0001c0002t0001g0001a0001c0002t0001g0105a0001c0002t0001g0117others(11): Show | 15 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.466+100T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153772 | ||||||
| chr19:48153773
|
C | T | 4 | a0001c0001t0004g0323a0001c0001t0004g0324a0001c0001t0004g0325others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+99G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153773 | ||||||
| chr19:48153819
|
T | TCCAC | 3 | a0001c0001t0004g0322a0001c0001t0004g0326a0001c0004t0004g0327 | 3 | NA18906.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.466+52_466+53insGT others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153819 | ||||||
| chr19:48153819
|
T | TCCACAC | 3 | a0001c0001t0004g0323a0001c0001t0004g0324a0001c0001t0004g0325 | 3 | HG02109.hp1 HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.466+52_466+53insGT others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153819 | ||||||
| chr19:48153819
|
T | TCCACACA others(1): Show |
8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 8 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+52_466+53insGT others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153819 | ||||||
| chr19:48153819
|
T | TCCACACA others(7): Show |
1 | a0003c0006t0001g0012 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.466+52_466+53insGT others(12): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153819 | ||||||
| chr19:48153819
|
T | TCCTCTTG others(5): Show |
1 | a0001c0003t0002g0028 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.466+52_466+53insGA others(10): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153819 | ||||||
| chr19:48153820
|
T | A | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.466+52A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCA | 40 | a0001c0002t0001g0043a0001c0002t0001g0046a0001c0002t0001g0070others(37): Show | 40 | HG00621.hp1 HG00733.hp1 HG01123.hp1 others(37): Show |
intron_variant | MODIFIER | c.466+50_466+51dupTG | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACA | 9 | a0001c0003t0002g0022a0001c0003t0002g0045a0001c0003t0002g0076others(6): Show | 9 | HG00738.hp2 HG01109.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.466+48_466+51dupTG others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACACA | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.466+46_466+51dupTG others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACACAC others(1): Show |
4 | a0001c0001t0001g0281a0001c0001t0001g0295a0001c0004t0003g0195others(1): Show | 4 | HG00639.hp1 HG01109.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+44_466+51dupTG others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACACAC others(3): Show |
9 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0226others(6): Show | 9 | HG01981.hp2 HG02148.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.466+42_466+51dupTG others(8): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACACAC others(5): Show |
49 | a0000c0013t0007g0182a0001c0001t0001g0225a0001c0001t0001g0227others(46): Show | 50 | HG00597.hp1 HG00673.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.466+40_466+51dupTG others(10): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACACAC others(7): Show |
27 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0223others(24): Show | 27 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.466+38_466+51dupTG others(12): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACACAC others(9): Show |
35 | a0001c0001t0001g0222a0001c0001t0001g0232a0001c0001t0001g0233others(32): Show | 35 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.466+36_466+51dupTG others(14): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACACAC others(11): Show |
21 | a0001c0001t0001g0221a0001c0001t0001g0241a0001c0001t0001g0242others(18): Show | 21 | HG00597.hp2 HG01167.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.466+34_466+51dupTG others(16): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACACAC others(13): Show |
8 | a0001c0001t0001g0274a0001c0001t0001g0280a0001c0001t0001g0286others(5): Show | 8 | HG00609.hp2 HG01975.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.466+32_466+51dupTG others(18): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
T | TCACACAC others(15): Show |
1 | a0001c0001t0001g0275 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.466+30_466+51dupTG others(20): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153820
|
TCACA | T | 4 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(1): Show | 4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.466+48_466+51delTG others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153820 | ||||||
| chr19:48153822
|
A | C | 1 | a0001c0002t0001g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.466+50T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 6/27 | chr19 | 48153822 | ||||||
| chr19:48153995
|
T | C | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.371-28A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48153995 | ||||||
| chr19:48154251
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.371-284T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48154251 | ||||||
| chr19:48154363
|
G | A | 75 | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0002t0001g0091others(72): Show | 76 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(73): Show |
intron_variant | MODIFIER | c.371-396C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48154363 | ||||||
| chr19:48154604
|
A | C | 1 | a0001c0003t0002g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.371-637T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48154604 | ||||||
| chr19:48154779
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.371-812G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48154779 | ||||||
| chr19:48154811
|
C | T | 1 | a0001c0003t0006g0004 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.371-844G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48154811 | ||||||
| chr19:48154829
|
G | A | 4 | a0001c0004t0003g0206a0001c0004t0003g0208a0001c0004t0003g0209others(1): Show | 4 | HG02809.hp1 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.371-862C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48154829 | ||||||
| chr19:48154896
|
C | T | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.371-929G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48154896 | ||||||
| chr19:48154902
|
T | G | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.371-935A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48154902 | ||||||
| chr19:48155025
|
A | G | 3 | a0001c0004t0003g0002a0001c0004t0003g0196a0001c0004t0003g0197 | 4 | HG02257.hp2 HG02717.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-1058T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155025 | ||||||
| chr19:48155038
|
T | C | 176 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.371-1071A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155038 | ||||||
| chr19:48155039
|
G | A | 10 | a0001c0001t0001g0237a0001c0001t0001g0276a0001c0001t0001g0277others(7): Show | 10 | HG00558.hp1 HG01975.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.371-1072C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155039 | ||||||
| chr19:48155263
|
C | T | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.371-1296G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155263 | ||||||
| chr19:48155281
|
C | T | 6 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.371-1314G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155281 | ||||||
| chr19:48155350
|
C | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-1383G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155350 | ||||||
| chr19:48155416
|
C | T | 1 | a0008c0012t0001g0244 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.371-1449G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155416 | ||||||
| chr19:48155425
|
G | A | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.371-1458C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155425 | ||||||
| chr19:48155493
|
A | C | 5 | a0001c0002t0001g0118a0001c0002t0001g0143a0001c0002t0001g0157others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.370+1521T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155493 | ||||||
| chr19:48155675
|
A | G | 160 | a0000c0013t0007g0182a0001c0001t0001g0095a0001c0001t0001g0134others(157): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.370+1339T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155675 | ||||||
| chr19:48155736
|
AAAATCC | A | 8 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0109others(5): Show | 8 | HG01934.hp1 HG01952.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.370+1272_370+1277d others(8): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155736 | ||||||
| chr19:48155794
|
T | A | 2 | a0001c0001t0001g0281a0001c0001t0001g0307 | 2 | HG00639.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.370+1220A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155794 | ||||||
| chr19:48155992
|
G | A | 2 | a0012c0024t0001g0101a0013c0023t0001g0102 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.370+1022C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48155992 | ||||||
| chr19:48156016
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017 | 3 | HG00735.hp1 HG00738.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.370+998G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156016 | ||||||
| chr19:48156021
|
T | C | 44 | a0001c0002t0001g0001a0001c0002t0001g0043a0001c0002t0001g0104others(41): Show | 45 | HG00558.hp2 HG00621.hp2 HG01934.hp1 others(42): Show |
intron_variant | MODIFIER | c.370+993A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156021 | ||||||
| chr19:48156048
|
A | C | 171 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(168): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.370+966T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156048 | ||||||
| chr19:48156071
|
C | T | 4 | a0001c0004t0001g0032a0001c0004t0001g0057a0001c0004t0001g0086others(1): Show | 4 | NA18955.hp1 NA18990.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.370+943G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156071 | ||||||
| chr19:48156152
|
G | A | 84 | a0001c0002t0001g0001a0001c0002t0001g0043a0001c0002t0001g0091others(81): Show | 85 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(82): Show |
intron_variant | MODIFIER | c.370+862C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156152 | ||||||
| chr19:48156166
|
C | T | 1 | a0001c0004t0003g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.370+848G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156166 | ||||||
| chr19:48156202
|
T | C | 1 | a0001c0002t0001g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.370+812A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156202 | ||||||
| chr19:48156300
|
G | GTCTCCC | 105 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.370+708_370+713dup others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156300 | ||||||
| chr19:48156413
|
C | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.370+601G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156413 | ||||||
| chr19:48156434
|
G | A | 44 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.370+580C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156434 | ||||||
| chr19:48156481
|
A | G | 252 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(249): Show | 254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.370+533T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156481 | ||||||
| chr19:48156608
|
G | T | 1 | a0001c0004t0003g0203 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.370+406C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156608 | ||||||
| chr19:48156634
|
T | A | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.370+380A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156634 | ||||||
| chr19:48156718
|
G | A | 1 | a0000c0013t0007g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.370+296C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156718 | ||||||
| chr19:48156770
|
G | A | 111 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.370+244C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156770 | ||||||
| chr19:48156810
|
G | A | 111 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.370+204C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156810 | ||||||
| chr19:48156938
|
C | CA | 41 | a0001c0001t0001g0228a0001c0001t0001g0238a0001c0001t0001g0282others(38): Show | 41 | HG00597.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.370+75dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156938 | ||||||
| chr19:48156938
|
CA | C | 19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG00733.hp2 HG00738.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.370+75delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156938 | ||||||
| chr19:48156938
|
CAA | C | 8 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.370+74_370+75delTT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156938 | ||||||
| chr19:48156941
|
A | G | 2 | a0001c0002t0001g0150a0007c0020t0001g0151 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.370+73T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156941 | ||||||
| chr19:48156959
|
A | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.370+55T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156959 | ||||||
| chr19:48156961
|
A | G | 19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.370+53T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156961 | ||||||
| chr19:48156981
|
C | T | 44 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.370+33G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156981 | ||||||
| chr19:48156986
|
GAAGGGGC others(1): Show |
G | 155 | a0000c0013t0007g0182a0001c0001t0001g0095a0001c0001t0001g0134others(152): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.370+20_370+27delTG others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48156986 | ||||||
| chr19:48157007
|
T | C | 3 | a0001c0004t0003g0002a0001c0004t0003g0196a0001c0004t0003g0197 | 4 | HG02257.hp2 HG02717.hp1 NA18522.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.370+7A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 5/27 | chr19 | 48157007 | ||||||
| chr19:48157188
|
T | C | 106 | a0001c0001t0001g0095a0001c0001t0001g0134a0001c0001t0001g0219others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.244-48A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157188 | ||||||
| chr19:48157254
|
A | G | 3 | a0001c0003t0002g0024a0001c0003t0002g0025a0001c0003t0002g0026 | 3 | HG00741.hp1 HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.244-114T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157254 | ||||||
| chr19:48157309
|
C | T | 16 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(13): Show | 16 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.244-169G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157309 | ||||||
| chr19:48157380
|
C | A | 2 | a0001c0002t0001g0138a0001c0002t0001g0163 | 2 | HG02257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.244-240G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157380 | ||||||
| chr19:48157380
|
C | T | 2 | a0001c0004t0003g0208a0001c0004t0003g0209 | 2 | HG02809.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.244-240G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157380 | ||||||
| chr19:48157404
|
A | G | 1 | a0001c0001t0001g0295 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.244-264T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157404 | ||||||
| chr19:48157434
|
T | C | 1 | a0001c0002t0001g0164 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.244-294A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157434 | ||||||
| chr19:48157682
|
T | C | 1 | a0001c0003t0002g0173 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.244-542A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157682 | ||||||
| chr19:48157693
|
C | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.244-553G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157693 | ||||||
| chr19:48157726
|
T | G | 1 | a0001c0001t0003g0207 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.244-586A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157726 | ||||||
| chr19:48157728
|
A | G | 1 | a0001c0002t0001g0156 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.244-588T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48157728 | ||||||
| chr19:48158036
|
A | G | 1 | a0001c0017t0002g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.244-896T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158036 | ||||||
| chr19:48158056
|
G | A | 1 | a0010c0010t0001g0085 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.244-916C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158056 | ||||||
| chr19:48158278
|
G | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.244-1138C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158278 | ||||||
| chr19:48158350
|
C | T | 104 | a0001c0001t0001g0095a0001c0001t0001g0219a0001c0001t0001g0220others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.244-1210G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158350 | ||||||
| chr19:48158366
|
G | GCCT | 150 | a0000c0013t0007g0182a0001c0001t0001g0095a0001c0001t0001g0219others(147): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.244-1229_244-1227d others(5): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158366 | ||||||
| chr19:48158421
|
G | C | 1 | a0001c0002t0001g0148 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.244-1281C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158421 | ||||||
| chr19:48158459
|
G | A | 2 | a0001c0002t0001g0139a0001c0002t0001g0140 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.244-1319C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158459 | ||||||
| chr19:48158612
|
G | A | 3 | a0001c0003t0002g0028a0001c0003t0002g0029a0001c0003t0002g0039 | 3 | NA18994.hp1 NA19058.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.244-1472C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158612 | ||||||
| chr19:48158616
|
C | G | 2 | a0001c0003t0002g0028a0001c0003t0002g0029 | 2 | NA19058.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.244-1476G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158616 | ||||||
| chr19:48158628
|
G | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0315 | 3 | HG00597.hp2 HG00609.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.244-1488C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158628 | ||||||
| chr19:48158678
|
C | T | 44 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.244-1538G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158678 | ||||||
| chr19:48158743
|
C | T | 1 | a0000c0013t0007g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.244-1603G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158743 | ||||||
| chr19:48158752
|
T | G | 44 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.244-1612A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158752 | ||||||
| chr19:48158830
|
C | G | 1 | a0013c0023t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.244-1690G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158830 | ||||||
| chr19:48158899
|
G | C | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-1759C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158899 | ||||||
| chr19:48158954
|
T | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.244-1814A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48158954 | ||||||
| chr19:48159080
|
A | ATT | 104 | a0001c0001t0001g0095a0001c0001t0001g0219a0001c0001t0001g0220others(101): Show | 104 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.244-1942_244-1941d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159080 | ||||||
| chr19:48159085
|
T | TTC | 44 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.244-1946_244-1945i others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159085 | ||||||
| chr19:48159147
|
G | T | 1 | a0001c0003t0002g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.244-2007C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159147 | ||||||
| chr19:48159284
|
C | T | 7 | a0001c0003t0002g0045a0001c0003t0002g0052a0001c0003t0002g0053others(4): Show | 7 | HG01433.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.243+2088G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159284 | ||||||
| chr19:48159336
|
T | C | 175 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(172): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.243+2036A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159336 | ||||||
| chr19:48159349
|
CGTGA | C | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.243+2019_243+2022d others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159349 | ||||||
| chr19:48159360
|
A | G | 251 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(248): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.243+2012T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159360 | ||||||
| chr19:48159366
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(1): Show | 4 | HG00423.hp2 NA18969.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+2006C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159366 | ||||||
| chr19:48159526
|
G | A | 106 | a0001c0001t0001g0095a0001c0001t0001g0219a0001c0001t0001g0220others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.243+1846C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159526 | ||||||
| chr19:48159601
|
G | C | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1771C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159601 | ||||||
| chr19:48159706
|
CTTAT | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.243+1662_243+1665d others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159706 | ||||||
| chr19:48159731
|
T | TTATC | 44 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.243+1640_243+1641i others(6): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159731 | ||||||
| chr19:48159780
|
C | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1592G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159780 | ||||||
| chr19:48159836
|
T | G | 170 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(167): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.243+1536A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159836 | ||||||
| chr19:48159862
|
C | T | 52 | a0000c0013t0007g0182a0001c0001t0001g0225a0001c0001t0001g0226others(49): Show | 53 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.243+1510G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159862 | ||||||
| chr19:48159867
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.243+1505C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159867 | ||||||
| chr19:48159875
|
G | A | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | NA18950.hp2 NA18973.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.243+1497C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159875 | ||||||
| chr19:48159925
|
GC | G | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1446delG | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159925 | ||||||
| chr19:48159939
|
A | G | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.243+1433T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48159939 | ||||||
| chr19:48160103
|
C | T | 2 | a0012c0024t0001g0101a0013c0023t0001g0102 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.243+1269G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160103 | ||||||
| chr19:48160157
|
G | A | 1 | a0001c0003t0002g0023 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.243+1215C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160157 | ||||||
| chr19:48160201
|
C | G | 2 | a0001c0002t0001g0106a0001c0002t0001g0165 | 2 | NA18991.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.243+1171G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160201 | ||||||
| chr19:48160204
|
C | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.243+1168G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160204 | ||||||
| chr19:48160322
|
G | A | 1 | a0005c0011t0003g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.243+1050C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160322 | ||||||
| chr19:48160340
|
G | C | 1 | a0002c0005t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.243+1032C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160340 | ||||||
| chr19:48160391
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+981C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160391 | ||||||
| chr19:48160414
|
C | T | 103 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.243+958G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160414 | ||||||
| chr19:48160556
|
A | G | 1 | a0001c0002t0001g0117 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.243+816T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160556 | ||||||
| chr19:48160595
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.243+777C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160595 | ||||||
| chr19:48160647
|
G | A | 1 | a0001c0004t0003g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.243+725C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160647 | ||||||
| chr19:48160654
|
G | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+718C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160654 | ||||||
| chr19:48160755
|
C | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+617G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160755 | ||||||
| chr19:48160819
|
A | G | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+553T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48160819 | ||||||
| chr19:48161236
|
G | C | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+136C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48161236 | ||||||
| chr19:48161267
|
G | A | 1 | a0001c0002t0001g0141 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.243+105C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48161267 | ||||||
| chr19:48161342
|
G | A | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+30C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 4/27 | chr19 | 48161342 | ||||||
| chr19:48161531
|
G | A | 1 | a0002c0005t0001g0006 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.108-24C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161531 | ||||||
| chr19:48161541
|
G | A | 103 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.108-34C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161541 | ||||||
| chr19:48161572
|
G | A | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.108-65C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161572 | ||||||
| chr19:48161608
|
C | T | 1 | a0001c0003t0002g0020 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.108-101G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161608 | ||||||
| chr19:48161690
|
G | A | 44 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.108-183C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161690 | ||||||
| chr19:48161794
|
T | C | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-287A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161794 | ||||||
| chr19:48161802
|
G | A | 105 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(102): Show | 105 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.108-295C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161802 | ||||||
| chr19:48161826
|
C | CT | 216 | a0000c0013t0007g0182a0001c0001t0001g0134a0001c0001t0001g0219others(213): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.108-320dupA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161826 | ||||||
| chr19:48161826
|
C | CTT | 9 | a0001c0001t0001g0220a0001c0001t0001g0238a0001c0001t0001g0245others(6): Show | 9 | HG02148.hp1 HG02486.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.108-321_108-320dup others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161826 | ||||||
| chr19:48161852
|
A | G | 174 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(171): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.108-345T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161852 | ||||||
| chr19:48161897
|
A | G | 174 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(171): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.107+365T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161897 | ||||||
| chr19:48161988
|
C | CGTGGCCA | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.107+267_107+273dup others(7): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161988 | ||||||
| chr19:48161999
|
G | A | 1 | a0001c0004t0003g0215 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107+263C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48161999 | ||||||
| chr19:48162161
|
T | C | 1 | a0001c0004t0004g0327 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.107+101A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 3/27 | chr19 | 48162161 | ||||||
| chr19:48162401
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.18-50G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162401 | ||||||
| chr19:48162433
|
C | CT | 22 | a0001c0001t0001g0219a0001c0001t0001g0239a0001c0001t0001g0240others(19): Show | 22 | HG00741.hp2 HG01346.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.18-83dupA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162433 | ||||||
| chr19:48162433
|
CT | C | 7 | a0001c0001t0001g0291a0001c0002t0001g0001a0001c0002t0001g0142others(4): Show | 8 | HG00639.hp2 HG02630.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.18-83delA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162433 | ||||||
| chr19:48162463
|
T | G | 1 | a0001c0001t0001g0317 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.18-112A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162463 | ||||||
| chr19:48162502
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.18-151G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162502 | ||||||
| chr19:48162519
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.18-168G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162519 | ||||||
| chr19:48162560
|
A | C | 4 | a0001c0004t0003g0174a0001c0004t0003g0203a0001c0004t0003g0204others(1): Show | 4 | HG00140.hp1 HG02572.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-209T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162560 | ||||||
| chr19:48162629
|
A | T | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.18-278T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162629 | ||||||
| chr19:48162634
|
C | T | 1 | a0001c0002t0001g0046 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.18-283G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162634 | ||||||
| chr19:48162635
|
G | A | 6 | a0001c0001t0004g0322a0001c0001t0004g0323a0001c0001t0004g0324others(3): Show | 6 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.18-284C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162635 | ||||||
| chr19:48162708
|
A | G | 174 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(171): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.18-357T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162708 | ||||||
| chr19:48162772
|
G | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-421C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162772 | ||||||
| chr19:48162852
|
C | T | 1 | a0001c0003t0002g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18-501G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162852 | ||||||
| chr19:48162923
|
C | CT | 176 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(173): Show | 177 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.18-573dupA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162923 | ||||||
| chr19:48162933
|
T | C | 1 | a0001c0002t0001g0111 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.18-582A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48162933 | ||||||
| chr19:48163017
|
C | T | 1 | a0001c0003t0002g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.18-666G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163017 | ||||||
| chr19:48163018
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.18-667C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163018 | ||||||
| chr19:48163107
|
G | A | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.18-756C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163107 | ||||||
| chr19:48163107
|
G | T | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-756C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163107 | ||||||
| chr19:48163201
|
T | A | 177 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.18-850A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163201 | ||||||
| chr19:48163208
|
G | A | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-857C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163208 | ||||||
| chr19:48163209
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.18-858G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163209 | ||||||
| chr19:48163210
|
G | A | 103 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.18-859C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163210 | ||||||
| chr19:48163225
|
AT | A | 153 | a0000c0013t0007g0182a0001c0001t0001g0219a0001c0001t0001g0220others(150): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.18-875delA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163225 | ||||||
| chr19:48163226
|
T | A | 1 | a0001c0003t0002g0087 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.18-875A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163226 | ||||||
| chr19:48163279
|
T | C | 5 | a0001c0001t0004g0323a0001c0001t0004g0324a0001c0001t0004g0325others(2): Show | 5 | HG02109.hp1 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.18-928A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163279 | ||||||
| chr19:48163291
|
G | A | 103 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.18-940C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163291 | ||||||
| chr19:48163332
|
C | G | 21 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(18): Show | 21 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.18-981G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163332 | ||||||
| chr19:48163341
|
C | G | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.18-990G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163341 | ||||||
| chr19:48163371
|
G | A | 2 | a0012c0024t0001g0101a0013c0023t0001g0102 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.18-1020C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163371 | ||||||
| chr19:48163379
|
G | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-1028C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163379 | ||||||
| chr19:48163468
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.18-1117C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163468 | ||||||
| chr19:48163511
|
G | A | 1 | a0001c0002t0001g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.18-1160C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163511 | ||||||
| chr19:48163583
|
C | T | 177 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.18-1232G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163583 | ||||||
| chr19:48163621
|
G | A | 1 | a0001c0003t0002g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.18-1270C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163621 | ||||||
| chr19:48163662
|
G | T | 103 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.18-1311C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163662 | ||||||
| chr19:48163726
|
G | A | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.18-1375C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163726 | ||||||
| chr19:48163742
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.18-1391C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163742 | ||||||
| chr19:48163817
|
C | G | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.18-1466G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163817 | ||||||
| chr19:48163818
|
G | C | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.18-1467C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163818 | ||||||
| chr19:48163860
|
G | A | 1 | a0001c0003t0002g0023 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.18-1509C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163860 | ||||||
| chr19:48163874
|
G | T | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.18-1523C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163874 | ||||||
| chr19:48163899
|
C | G | 67 | a0001c0001t0001g0134a0001c0002t0001g0001a0001c0002t0001g0104others(64): Show | 68 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.18-1548G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163899 | ||||||
| chr19:48163924
|
G | A | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.18-1573C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163924 | ||||||
| chr19:48163944
|
C | CA | 17 | a0001c0002t0001g0091a0001c0002t0001g0143a0001c0002t0001g0144others(14): Show | 17 | HG00673.hp2 HG01175.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.18-1594dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163944 | ||||||
| chr19:48163944
|
CA | C | 146 | a0000c0013t0007g0182a0001c0001t0001g0219a0001c0001t0001g0220others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.18-1594delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163944 | ||||||
| chr19:48163982
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.17+1568T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48163982 | ||||||
| chr19:48164034
|
A | C | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.17+1516T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164034 | ||||||
| chr19:48164117
|
G | A | 103 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.17+1433C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164117 | ||||||
| chr19:48164185
|
G | A | 3 | a0001c0002t0001g0146a0001c0002t0001g0147a0001c0002t0001g0148 | 3 | HG00621.hp2 NA18952.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.17+1365C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164185 | ||||||
| chr19:48164295
|
C | T | 1 | a0001c0004t0003g0180 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.17+1255G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164295 | ||||||
| chr19:48164431
|
T | C | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.17+1119A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164431 | ||||||
| chr19:48164432
|
C | T | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.17+1118G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164432 | ||||||
| chr19:48164481
|
T | C | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.17+1069A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164481 | ||||||
| chr19:48164552
|
C | T | 1 | a0002c0005t0001g0007 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.17+998G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164552 | ||||||
| chr19:48164586
|
C | A | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.17+964G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164586 | ||||||
| chr19:48164601
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.17+949G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164601 | ||||||
| chr19:48164670
|
G | C | 1 | a0005c0011t0003g0201 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.17+880C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164670 | ||||||
| chr19:48164679
|
T | A | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.17+871A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164679 | ||||||
| chr19:48164687
|
A | C | 1 | a0012c0024t0001g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.17+863T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164687 | ||||||
| chr19:48164719
|
T | G | 1 | a0013c0023t0001g0102 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.17+831A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164719 | ||||||
| chr19:48164861
|
G | C | 2 | a0001c0001t0004g0326a0001c0004t0004g0327 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.17+689C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164861 | ||||||
| chr19:48164879
|
T | C | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.17+671A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164879 | ||||||
| chr19:48164932
|
A | G | 2 | a0012c0024t0001g0101a0013c0023t0001g0102 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.17+618T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164932 | ||||||
| chr19:48164959
|
C | G | 1 | a0001c0003t0002g0044 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.17+591G>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164959 | ||||||
| chr19:48164986
|
C | T | 2 | a0012c0024t0001g0101a0013c0023t0001g0102 | 2 | HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.17+564G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48164986 | ||||||
| chr19:48165238
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.17+312C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48165238 | ||||||
| chr19:48165272
|
C | T | 2 | a0003c0006t0001g0009a0003c0006t0001g0010 | 2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.17+278G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48165272 | ||||||
| chr19:48165452
|
A | G | 177 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.17+98T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48165452 | ||||||
| chr19:48165473
|
T | G | 2 | a0001c0001t0004g0326a0001c0004t0004g0327 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.17+77A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48165473 | ||||||
| chr19:48165506
|
G | A | 2 | a0002c0005t0001g0007a0002c0005t0001g0008 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.17+44C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48165506 | ||||||
| chr19:48165538
|
G | A | 103 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.17+12C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 2/27 | chr19 | 48165538 | ||||||
| chr19:48165657
|
T | C | 68 | a0001c0001t0001g0134a0001c0002t0001g0001a0001c0002t0001g0043others(65): Show | 69 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.-57-34A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48165657 | ||||||
| chr19:48165709
|
G | GA | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.-57-87dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48165709 | ||||||
| chr19:48165709
|
G | GAA | 48 | a0000c0013t0007g0182a0001c0001t0001g0234a0001c0001t0003g0177others(45): Show | 49 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.-57-88_-57-87dupTT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48165709 | ||||||
| chr19:48165903
|
GT | G | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57-281delA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48165903 | ||||||
| chr19:48166015
|
T | C | 154 | a0000c0013t0007g0182a0001c0001t0001g0219a0001c0001t0001g0220others(151): Show | 155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.-57-392A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166015 | ||||||
| chr19:48166115
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-57-492C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166115 | ||||||
| chr19:48166117
|
T | C | 171 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(168): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-57-494A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166117 | ||||||
| chr19:48166170
|
G | A | 1 | a0001c0003t0002g0094 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-57-547C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166170 | ||||||
| chr19:48166200
|
C | A | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-57-577G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166200 | ||||||
| chr19:48166256
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | NA18950.hp2 NA18973.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-633C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166256 | ||||||
| chr19:48166371
|
T | A | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0305 | 3 | HG01346.hp1 HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-57-748A>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166371 | ||||||
| chr19:48166491
|
C | T | 107 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-57-868G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166491 | ||||||
| chr19:48166493
|
C | T | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.-57-870G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166493 | ||||||
| chr19:48166493
|
CCTCAGGA others(8): Show |
C | 68 | a0001c0001t0001g0134a0001c0002t0001g0001a0001c0002t0001g0043others(65): Show | 69 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(66): Show |
intron_variant | MODIFIER | c.-57-885_-57-871del others(15): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166493 | ||||||
| chr19:48166608
|
A | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57-985T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166608 | ||||||
| chr19:48166701
|
T | G | 1 | a0001c0001t0001g0095 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-57-1078A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166701 | ||||||
| chr19:48166795
|
A | C | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57-1172T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166795 | ||||||
| chr19:48166902
|
T | C | 160 | a0000c0013t0007g0182a0001c0001t0001g0219a0001c0001t0001g0220others(157): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.-57-1279A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166902 | ||||||
| chr19:48166950
|
ACT | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57-1329_-57-1328d others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166950 | ||||||
| chr19:48166959
|
C | CA | 10 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(7): Show | 10 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-57-1337dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166959 | ||||||
| chr19:48166959
|
CA | C | 112 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-57-1337delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166959 | ||||||
| chr19:48166969
|
AAAAAAGA others(3): Show |
A | 46 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(43): Show | 47 | HG00140.hp1 HG01071.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.-57-1356_-57-1347d others(12): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166969 | ||||||
| chr19:48166975
|
G | C | 4 | a0001c0002t0001g0106a0001c0002t0001g0149a0001c0002t0001g0164others(1): Show | 4 | NA18973.hp1 NA18991.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-1352C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48166975 | ||||||
| chr19:48167094
|
C | T | 8 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0109others(5): Show | 8 | HG01934.hp1 HG01952.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57-1471G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167094 | ||||||
| chr19:48167204
|
G | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57-1581C>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167204 | ||||||
| chr19:48167233
|
A | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57-1610T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167233 | ||||||
| chr19:48167396
|
T | C | 1 | a0001c0002t0001g0165 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-57-1773A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167396 | ||||||
| chr19:48167419
|
G | A | 2 | a0001c0002t0001g0150a0007c0020t0001g0151 | 2 | HG02145.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-57-1796C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167419 | ||||||
| chr19:48167456
|
G | A | 103 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-57-1833C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167456 | ||||||
| chr19:48167553
|
A | G | 177 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-57-1930T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167553 | ||||||
| chr19:48167751
|
A | T | 1 | a0001c0001t0001g0234 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-57-2128T>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167751 | ||||||
| chr19:48167818
|
C | T | 171 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(168): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-57-2195G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167818 | ||||||
| chr19:48167825
|
T | TA | 18 | a0001c0002t0001g0152a0001c0002t0001g0153a0001c0002t0001g0154others(15): Show | 18 | HG00673.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57-2203dupT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167825 | ||||||
| chr19:48167825
|
TA | T | 27 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(24): Show | 27 | HG00639.hp2 HG00733.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-57-2203delT | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167825 | ||||||
| chr19:48167825
|
TAAAAAAA | T | 13 | a0001c0003t0002g0028a0001c0003t0002g0029a0001c0003t0002g0030others(10): Show | 13 | HG00621.hp1 HG02135.hp2 NA18961.hp2 others(10): Show |
intron_variant | MODIFIER | c.-57-2209_-57-2203d others(9): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167825 | ||||||
| chr19:48167835
|
A | C | 1 | a0001c0001t0001g0232 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-57-2212T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167835 | ||||||
| chr19:48167840
|
A | AC | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0321 | 3 | HG02559.hp1 HG03453.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-57-2218_-57-2217i others(3): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167840 | ||||||
| chr19:48167840
|
A | C | 169 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(166): Show | 170 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.-57-2217T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167840 | ||||||
| chr19:48167845
|
A | C | 177 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-57-2222T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167845 | ||||||
| chr19:48167851
|
C | A | 4 | a0001c0002t0001g0166a0001c0002t0001g0167a0001c0002t0001g0172others(1): Show | 4 | HG02451.hp2 HG02683.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57-2228G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167851 | ||||||
| chr19:48167856
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57-2233T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48167856 | ||||||
| chr19:48168005
|
G | A | 4 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(1): Show | 4 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+2236C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168005 | ||||||
| chr19:48168146
|
G | A | 107 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-58+2095C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168146 | ||||||
| chr19:48168146
|
G | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(3): Show | 6 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.-58+2095C>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168146 | ||||||
| chr19:48168235
|
C | T | 1 | a0009c0016t0002g0027 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-58+2006G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168235 | ||||||
| chr19:48168332
|
A | C | 177 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-58+1909T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168332 | ||||||
| chr19:48168346
|
A | G | 107 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(104): Show | 107 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-58+1895T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168346 | ||||||
| chr19:48168418
|
A | C | 6 | a0001c0002t0001g0168a0001c0002t0001g0169a0001c0002t0001g0170others(3): Show | 6 | HG01891.hp1 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-58+1823T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168418 | ||||||
| chr19:48168521
|
G | A | 1 | a0001c0004t0003g0178 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-58+1720C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168521 | ||||||
| chr19:48168721
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-58+1520A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168721 | ||||||
| chr19:48168874
|
C | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+1367G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168874 | ||||||
| chr19:48168880
|
A | G | 1 | a0001c0002t0001g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-58+1361T>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168880 | ||||||
| chr19:48168885
|
G | A | 177 | a0000c0013t0007g0182a0001c0001t0001g0013a0001c0001t0001g0014others(174): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-58+1356C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48168885 | ||||||
| chr19:48169130
|
TC | T | 3 | a0001c0003t0002g0024a0001c0003t0002g0025a0001c0003t0002g0026 | 3 | HG00741.hp1 HG01358.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-58+1110delG | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169130 | ||||||
| chr19:48169302
|
C | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+939G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169302 | ||||||
| chr19:48169381
|
A | C | 4 | a0001c0003t0002g0020a0001c0003t0002g0021a0001c0003t0002g0022others(1): Show | 4 | HG02083.hp2 HG03491.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+860T>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169381 | ||||||
| chr19:48169415
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-58+826A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169415 | ||||||
| chr19:48169460
|
T | G | 1 | a0001c0002t0001g0019 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-58+781A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169460 | ||||||
| chr19:48169617
|
G | A | 2 | a0001c0004t0003g0203a0001c0004t0003g0204 | 2 | HG02572.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-58+624C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169617 | ||||||
| chr19:48169641
|
G | A | 1 | a0001c0001t0001g0308 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-58+600C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169641 | ||||||
| chr19:48169691
|
G | GCCCCGCC others(21): Show |
1 | a0001c0001t0001g0309 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-58+522_-58+549dup others(28): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169691 | ||||||
| chr19:48169743
|
T | C | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.-58+498A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169743 | ||||||
| chr19:48169790
|
G | A | 1 | a0001c0003t0002g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-58+451C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169790 | ||||||
| chr19:48169907
|
G | GT | 10 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(7): Show | 10 | HG01981.hp2 HG02148.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.-58+333dupA | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169907 | ||||||
| chr19:48169909
|
T | TC | 27 | a0000c0013t0007g0182a0001c0001t0003g0183a0001c0001t0003g0202others(24): Show | 28 | HG01109.hp2 HG01123.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-58+331_-58+332ins others(1): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169909 | ||||||
| chr19:48169909
|
T | TCC | 11 | a0001c0001t0003g0207a0001c0004t0003g0205a0001c0004t0003g0206others(8): Show | 11 | HG00140.hp1 HG02040.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.-58+331_-58+332ins others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169909 | ||||||
| chr19:48169909
|
T | TCCC | 4 | a0001c0001t0003g0217a0001c0002t0003g0218a0001c0004t0003g0216others(1): Show | 4 | HG00673.hp1 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-58+331_-58+332ins others(3): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169909 | ||||||
| chr19:48169910
|
T | C | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.-58+331A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169910 | ||||||
| chr19:48169911
|
T | C | 51 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(48): Show | 52 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.-58+330A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169911 | ||||||
| chr19:48169911
|
T | TTC | 78 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.-58+329_-58+330ins others(2): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169911 | ||||||
| chr19:48169911
|
T | TTCC | 9 | a0001c0001t0001g0310a0001c0001t0001g0311a0001c0001t0001g0312others(6): Show | 9 | HG00597.hp1 HG00597.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.-58+329_-58+330ins others(3): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169911 | ||||||
| chr19:48169911
|
T | TTCCC | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG01074.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-58+329_-58+330ins others(4): Show |
LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169911 | ||||||
| chr19:48169911
|
TC | T | 19 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(16): Show | 19 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-58+329delG | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169911 | ||||||
| chr19:48169912
|
C | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+329G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169912 | ||||||
| chr19:48169913
|
C | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(14): Show | 17 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.-58+328G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169913 | ||||||
| chr19:48169916
|
C | A | 1 | a0001c0003t0002g0100 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-58+325G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169916 | ||||||
| chr19:48169946
|
C | A | 1 | a0001c0002t0001g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-58+295G>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169946 | ||||||
| chr19:48169955
|
T | C | 197 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(194): Show | 198 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.-58+286A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48169955 | ||||||
| chr19:48170034
|
T | C | 1 | a0001c0003t0002g0173 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-58+207A>G | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48170034 | ||||||
| chr19:48170047
|
T | G | 47 | a0000c0013t0007g0182a0001c0001t0003g0177a0001c0001t0003g0183others(44): Show | 48 | HG00140.hp1 HG00673.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.-58+194A>C | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48170047 | ||||||
| chr19:48170171
|
C | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(8): Show | 11 | HG00733.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.-58+70G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48170171 | ||||||
| chr19:48170201
|
G | A | 103 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0221others(100): Show | 103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-58+40C>T | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48170201 | ||||||
| chr19:48170207
|
C | T | 4 | a0002c0005t0001g0005a0002c0005t0001g0006a0002c0005t0001g0007others(1): Show | 4 | HG02486.hp1 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-58+34G>A | LIG1 | ENSG00000105486.15 | transcript | ENST00000263274.12 | protein_coding | 1/27 | chr19 | 48170207 |