| geneid | 353299 |
|---|---|
| ensemblid | ENSG00000121446.20 |
| hgncid | 18636 |
| symbol | RGSL1 |
| name | regulator of G protein signaling like 1 |
| refseq_nuc | NM_001137669.2 |
| refseq_prot | NP_001131141.1 |
| ensembl_nuc | ENST00000294854.13 |
| ensembl_prot | ENSP00000457748.1 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 182450146 |
| end | 182560597 |
| strand | + |
| ver | v1.2 |
| region | chr1:182450146-182560597 |
| region5000 | chr1:182445146-182565597 |
| regionname0 | RGSL1_chr1_182450146_182560597 |
| regionname5000 | RGSL1_chr1_182445146_182565597 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1076 | 170 | 53 | 36 | 54 | 10 | 15 | 38 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0002 | 0/0 | 1076 | 76 | 8 | 12 | 46 | 2 | 8 | 37 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0003 | 0/0 | 1076 | 68 | 12 | 10 | 40 | 1 | 5 | 31 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0004 | 0/0 | 1076 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0005 | 0/0 | 1076 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0006 | 0/0 | 1076 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0007 | 0/0 | 1076 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0008 | 0/0 | 1076 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0009 | 0/0 | 1076 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0010 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0011 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0012 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0013 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0014 | 0/0 | 1076 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0015 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0016 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0017 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3231 | 93 | 21 | 21 | 37 | 6 | 8 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0002 | 0/0 | 3231 | 76 | 8 | 12 | 46 | 2 | 8 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0003 | 0/0 | 3231 | 67 | 11 | 10 | 40 | 1 | 5 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0004 | 1/1 | 3231 | 59 | 14 | 15 | 17 | 4 | 7 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0005 | 0/0 | 3231 | 8 | 8 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0006 | 0/0 | 3231 | 5 | 5 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0007 | 0/0 | 3231 | 4 | 4 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0008 | 0/0 | 3231 | 3 | 0 | 0 | 0 | 1 | 2 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0009 | 0/0 | 3231 | 3 | 2 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0010 | 0/0 | 3231 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0011 | 0/0 | 3231 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0012 | 0/0 | 3231 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0013 | 0/0 | 3231 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0014 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0015 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0016 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0017 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0018 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0019 | 0/0 | 3231 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0020 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0021 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0022 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0023 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0024 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| c0025 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 505 | 295 | 78 | 50 | 125 | 14 | 26 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| t0002 | 0/0 | 505 | 43 | 8 | 10 | 21 | 0 | 4 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0322 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3231 | 93 | 21 | 21 | 37 | 6 | 8 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0004 | 1/1 | 3231 | 59 | 14 | 15 | 17 | 4 | 7 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0005 | 0/0 | 3231 | 8 | 8 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0006 | 0/0 | 3231 | 5 | 5 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0007 | 0/0 | 3231 | 4 | 4 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0017 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0002c0002 | 0/0 | 3231 | 76 | 8 | 12 | 46 | 2 | 8 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0003c0003 | 0/0 | 3231 | 67 | 11 | 10 | 40 | 1 | 5 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0003c0024 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0004c0009 | 0/0 | 3231 | 3 | 2 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0004c0012 | 0/0 | 3231 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0005c0008 | 0/0 | 3231 | 3 | 0 | 0 | 0 | 1 | 2 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0006c0013 | 0/0 | 3231 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0007c0018 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0007c0020 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0008c0010 | 0/0 | 3231 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0009c0011 | 0/0 | 3231 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0010c0025 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0011c0023 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0012c0015 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0013c0016 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0014c0019 | 0/0 | 3231 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0015c0021 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0016c0022 | 0/0 | 3231 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0017c0014 | 0/0 | 3231 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3735 | 93 | 21 | 21 | 37 | 6 | 8 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0004t0001 | 1/1 | 3735 | 51 | 14 | 14 | 10 | 4 | 7 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0004t0002 | 0/0 | 3735 | 8 | 0 | 1 | 7 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0005t0001 | 0/0 | 3735 | 8 | 8 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0006t0001 | 0/0 | 3735 | 5 | 5 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0007t0001 | 0/0 | 3735 | 4 | 4 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0001c0017t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0002c0002t0001 | 0/0 | 3735 | 74 | 8 | 11 | 46 | 2 | 7 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0002c0002t0002 | 0/0 | 3735 | 2 | 0 | 1 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0003c0003t0001 | 0/0 | 3735 | 35 | 3 | 2 | 27 | 1 | 2 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0003c0003t0002 | 0/0 | 3735 | 32 | 8 | 8 | 13 | 0 | 3 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0003c0024t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0004c0009t0001 | 0/0 | 3735 | 3 | 2 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0004c0012t0001 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0005c0008t0001 | 0/0 | 3735 | 3 | 0 | 0 | 0 | 1 | 2 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0006c0013t0001 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0007c0018t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0007c0020t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0008c0010t0001 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0009c0011t0001 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0010c0025t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0011c0023t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0012c0015t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0013c0016t0002 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0014c0019t0001 | 0/0 | 3735 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0015c0021t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0016c0022t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| a0017c0014t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | copy fasta | chr1 | 182445146 | 182565597 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0322 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0004t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0005t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0005t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0005t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0005t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0005t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0006t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0006t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0006t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0006t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0006t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0007t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0007t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0007t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0001c0017t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0003c0024t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0004c0009t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0004c0009t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0004c0009t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0004c0012t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0004c0012t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0005c0008t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0005c0008t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0005c0008t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0006c0013t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0006c0013t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0007c0018t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0007c0020t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0008c0010t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0008c0010t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0009c0011t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0009c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0010c0025t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0011c0023t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0012c0015t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0013c0016t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0014c0019t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0015c0021t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0016c0022t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| a0017c0014t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0001 | g0318 | EUR | GBR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0033 | EUR | GBR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0230 | EUR | GBR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00140 | hp2 | a0005 | c0008 | t0001 | g0080 | EUR | GBR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0150 | EUR | FIN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00423 | hp1 | a0013 | c0016 | t0002 | g0007 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00423 | hp2 | a0001 | c0004 | t0001 | g0285 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00544 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00558 | hp2 | a0015 | c0021 | t0001 | g0164 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00609 | hp2 | a0003 | c0003 | t0001 | g0039 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00639 | hp1 | a0003 | c0003 | t0002 | g0255 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0315 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0300 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0258 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00735 | hp1 | a0001 | c0004 | t0001 | g0319 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG00741 | hp2 | a0001 | c0004 | t0002 | g0130 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01069 | hp2 | a0003 | c0003 | t0002 | g0005 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01070 | hp2 | a0001 | c0004 | t0001 | g0111 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01071 | hp1 | a0003 | c0003 | t0002 | g0005 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0129 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01074 | hp1 | a0003 | c0003 | t0002 | g0215 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01099 | hp1 | a0001 | c0004 | t0001 | g0192 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01099 | hp2 | a0004 | c0009 | t0001 | g0221 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01109 | hp1 | a0001 | c0004 | t0001 | g0187 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0279 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0317 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01192 | hp1 | a0003 | c0003 | t0002 | g0310 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01243 | hp2 | a0014 | c0019 | t0001 | g0228 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01255 | hp1 | a0001 | c0004 | t0001 | g0257 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01255 | hp2 | a0001 | c0004 | t0001 | g0231 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0288 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0275 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01516 | hp2 | a0001 | c0004 | t0001 | g0232 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01884 | hp1 | a0009 | c0011 | t0001 | g0186 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01891 | hp1 | a0001 | c0006 | t0001 | g0209 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0180 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0235 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01975 | hp2 | a0001 | c0004 | t0001 | g0286 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01981 | hp1 | a0003 | c0003 | t0001 | g0292 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01981 | hp2 | a0003 | c0003 | t0002 | g0251 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0287 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0314 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02015 | hp2 | a0003 | c0003 | t0002 | g0236 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02027 | hp1 | a0003 | c0003 | t0002 | g0324 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0128 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0259 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02129 | hp2 | a0001 | c0004 | t0001 | g0312 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0053 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0329 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02148 | hp1 | a0003 | c0003 | t0002 | g0264 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | CDX | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CDX | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | CDX | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | CDX | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02257 | hp1 | a0004 | c0009 | t0001 | g0220 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02257 | hp2 | a0001 | c0004 | t0001 | g0177 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0105 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02258 | hp2 | a0001 | c0005 | t0001 | g0171 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0062 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02280 | hp1 | a0008 | c0010 | t0001 | g0206 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02280 | hp2 | a0003 | c0003 | t0002 | g0028 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02293 | hp1 | a0003 | c0003 | t0002 | g0291 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0217 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0110 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0325 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0112 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02602 | hp2 | a0001 | c0004 | t0001 | g0283 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02615 | hp2 | a0003 | c0003 | t0002 | g0026 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02622 | hp2 | a0001 | c0007 | t0001 | g0194 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0271 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0313 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0023 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02717 | hp1 | a0001 | c0005 | t0001 | g0268 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02717 | hp2 | a0001 | c0004 | t0001 | g0107 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02809 | hp2 | a0003 | c0003 | t0001 | g0029 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02818 | hp2 | a0003 | c0003 | t0001 | g0117 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02895 | hp1 | a0001 | c0017 | t0001 | g0065 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02895 | hp2 | a0003 | c0003 | t0002 | g0059 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0328 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02896 | hp2 | a0004 | c0012 | t0001 | g0326 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02897 | hp1 | a0004 | c0012 | t0001 | g0222 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02897 | hp2 | a0003 | c0003 | t0002 | g0025 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02922 | hp2 | a0003 | c0024 | t0001 | g0104 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02965 | hp1 | a0001 | c0007 | t0001 | g0212 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0188 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02970 | hp2 | a0012 | c0015 | t0001 | g0049 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02976 | hp1 | a0017 | c0014 | t0001 | g0167 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0016 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0203 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0211 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03130 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03130 | hp2 | a0001 | c0005 | t0001 | g0330 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03195 | hp1 | a0001 | c0006 | t0001 | g0174 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03195 | hp2 | a0001 | c0007 | t0001 | g0022 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03209 | hp1 | a0010 | c0025 | t0001 | g0226 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03225 | hp1 | a0004 | c0009 | t0001 | g0225 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03225 | hp2 | a0001 | c0005 | t0001 | g0010 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03239 | hp1 | a0005 | c0008 | t0001 | g0042 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03453 | hp1 | a0001 | c0005 | t0001 | g0108 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0270 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03486 | hp1 | a0008 | c0010 | t0001 | g0205 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03486 | hp2 | a0003 | c0003 | t0002 | g0057 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03490 | hp2 | a0001 | c0004 | t0001 | g0282 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0106 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0214 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0115 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0040 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0293 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03831 | hp1 | a0003 | c0003 | t0002 | g0015 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03834 | hp1 | a0005 | c0008 | t0001 | g0013 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0321 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0252 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03927 | hp2 | a0001 | c0004 | t0001 | g0009 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG04184 | hp2 | a0003 | c0003 | t0002 | g0256 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG04204 | hp1 | a0003 | c0003 | t0002 | g0058 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0229 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0116 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18522 | hp1 | a0006 | c0013 | t0001 | g0223 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18522 | hp2 | a0001 | c0006 | t0001 | g0210 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18612 | hp1 | a0003 | c0003 | t0001 | g0159 | EAS | CHB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18906 | hp1 | a0001 | c0005 | t0001 | g0327 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18906 | hp2 | a0009 | c0011 | t0001 | g0185 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18939 | hp2 | a0003 | c0003 | t0002 | g0132 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18941 | hp1 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18947 | hp1 | a0001 | c0004 | t0001 | g0124 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0262 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0145 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18950 | hp2 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18962 | hp2 | a0001 | c0004 | t0001 | g0276 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18965 | hp1 | a0001 | c0004 | t0002 | g0054 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18966 | hp1 | a0003 | c0003 | t0002 | g0024 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18966 | hp2 | a0016 | c0022 | t0001 | g0073 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18968 | hp1 | a0003 | c0003 | t0002 | g0061 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18969 | hp1 | a0003 | c0003 | t0001 | g0237 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18969 | hp2 | a0001 | c0004 | t0001 | g0125 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18973 | hp2 | a0003 | c0003 | t0002 | g0091 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18975 | hp1 | a0001 | c0004 | t0002 | g0281 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18980 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18986 | hp2 | a0001 | c0004 | t0001 | g0284 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18989 | hp1 | a0007 | c0018 | t0001 | g0298 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA18994 | hp2 | a0003 | c0003 | t0002 | g0060 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19004 | hp2 | a0001 | c0004 | t0002 | g0044 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19010 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0183 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19043 | hp1 | a0001 | c0004 | t0001 | g0170 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19043 | hp2 | a0003 | c0003 | t0002 | g0027 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19056 | hp1 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19058 | hp1 | a0001 | c0004 | t0002 | g0163 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19066 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19070 | hp1 | a0001 | c0004 | t0001 | g0082 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19070 | hp2 | a0001 | c0004 | t0002 | g0055 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19074 | hp1 | a0003 | c0003 | t0002 | g0161 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19078 | hp1 | a0001 | c0004 | t0001 | g0092 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19078 | hp2 | a0001 | c0004 | t0002 | g0123 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19079 | hp2 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19082 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19082 | hp2 | a0001 | c0004 | t0001 | g0234 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19084 | hp1 | a0007 | c0020 | t0001 | g0020 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0227 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19086 | hp1 | a0011 | c0023 | t0001 | g0134 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19087 | hp1 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19089 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19091 | hp1 | a0003 | c0003 | t0001 | g0089 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19240 | hp1 | a0001 | c0006 | t0001 | g0208 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0189 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA20752 | hp1 | a0001 | c0004 | t0001 | g0316 | EUR | TSI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0100 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02109 | hp1 | a0006 | c0013 | t0001 | g0224 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02559 | hp1 | a0001 | c0006 | t0001 | g0173 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG06807 | hp1 | a0003 | c0003 | t0002 | g0018 | AFR | USA | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | USA | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | USA | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0290 | AFR | USA | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| NA21309 | hp2 | a0003 | c0003 | t0002 | g0179 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0001 | g0323 | REF | REF | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0322 | REF | REF | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:182453959
|
G | T | 3 | a0004a0006a0010 | 8 | HG01099.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.15G>T | p.Glu5Asp | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/22 | 35/3735 | 15/3231 | 5/1076 | chr1 | 182453959 | ||
| chr1:182454011
|
G | A | 2 | a0005a0017 | 4 | HG00140.hp2 HG02976.hp1 HG03239.hp1 others(1): Show |
missense_variant | MODERATE | c.67G>A | p.Asp23Asn | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/22 | 87/3735 | 67/3231 | 23/1076 | chr1 | 182454011 | ||
| chr1:182472452
|
A | C | 1 | a0011 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.358A>C | p.Met120Leu | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/22 | 378/3735 | 358/3231 | 120/1076 | chr1 | 182472452 | ||
| chr1:182472552
|
A | G | 1 | a0016 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.458A>G | p.Asn153Ser | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/22 | 478/3735 | 458/3231 | 153/1076 | chr1 | 182472552 | ||
| chr1:182473626
|
G | A | 1 | a0012 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.515G>A | p.Arg172Lys | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 535/3735 | 515/3231 | 172/1076 | chr1 | 182473626 | ||
| chr1:182473879
|
G | C | 5 | a0003a0010a0012others(2): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
missense_variant | MODERATE | c.768G>C | p.Trp256Cys | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 788/3735 | 768/3231 | 256/1076 | chr1 | 182473879 | ||
| chr1:182474354
|
A | T | 1 | a0009 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1243A>T | p.Asn415Tyr | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 1263/3735 | 1243/3231 | 415/1076 | chr1 | 182474354 | ||
| chr1:182488987
|
A | G | 1 | a0009 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1502A>G | p.Asn501Ser | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/22 | 1522/3735 | 1502/3231 | 501/1076 | chr1 | 182488987 | ||
| chr1:182527656
|
T | G | 1 | a0009 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.2009T>G | p.Ile670Ser | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/22 | 2029/3735 | 2009/3231 | 670/1076 | chr1 | 182527656 | ||
| chr1:182527694
|
A | G | 6 | a0002a0005a0006others(3): Show | 84 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(81): Show |
missense_variant | MODERATE | c.2047A>G | p.Ile683Val | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/22 | 2067/3735 | 2047/3231 | 683/1076 | chr1 | 182527694 | ||
| chr1:182530295
|
G | A | 1 | a0013 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.2177G>A | p.Arg726His | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/22 | 2197/3735 | 2177/3231 | 726/1076 | chr1 | 182530295 | ||
| chr1:182530808
|
C | G | 1 | a0008 | 2 | HG02280.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.2262C>G | p.Asp754Glu | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/22 | 2282/3735 | 2262/3231 | 754/1076 | chr1 | 182530808 | ||
| chr1:182530821
|
C | T | 1 | a0009 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.2275C>T | p.His759Tyr | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/22 | 2295/3735 | 2275/3231 | 759/1076 | chr1 | 182530821 | ||
| chr1:182530822
|
A | G | 1 | a0009 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.2276A>G | p.His759Arg | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/22 | 2296/3735 | 2276/3231 | 759/1076 | chr1 | 182530822 | ||
| chr1:182540307
|
G | A | 1 | a0015 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.2555G>A | p.Ser852Asn | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/22 | 2575/3735 | 2555/3231 | 852/1076 | chr1 | 182540307 | ||
| chr1:182548782
|
C | G | 1 | a0014 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.2891C>G | p.Ala964Gly | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/22 | 2911/3735 | 2891/3231 | 964/1076 | chr1 | 182548782 | ||
| chr1:182553515
|
G | A | 1 | a0007 | 2 | NA18989.hp1 NA19084.hp1 |
missense_variant | MODERATE | c.3104G>A | p.Arg1035Gln | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/22 | 3124/3735 | 3104/3231 | 1035/1076 | chr1 | 182553515 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:182472433
|
C | T | 1 | a0003c0024 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.339C>T | p.Asn113Asn | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/22 | 359/3735 | 339/3231 | 113/1076 | chr1 | 182472433 | ||
| chr1:182473975
|
G | A | 2 | a0001c0006a0001c0017 | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
synonymous_variant | LOW | c.864G>A | p.Val288Val | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 884/3735 | 864/3231 | 288/1076 | chr1 | 182473975 | ||
| chr1:182474327
|
T | C | 15 | a0001c0001a0001c0005a0001c0006others(12): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
synonymous_variant | LOW | c.1216T>C | p.Leu406Leu | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 1236/3735 | 1216/3231 | 406/1076 | chr1 | 182474327 | ||
| chr1:182532766
|
C | T | 1 | a0009c0011 | 2 | HG01884.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.2469C>T | p.His823His | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/22 | 2489/3735 | 2469/3231 | 823/1076 | chr1 | 182532766 | ||
| chr1:182540254
|
C | T | 3 | a0001c0005a0001c0007a0001c0017 | 13 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(10): Show |
synonymous_variant | LOW | c.2502C>T | p.Thr834Thr | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/22 | 2522/3735 | 2502/3231 | 834/1076 | chr1 | 182540254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:182560449
|
T | C | 4 | a0001c0004t0002a0002c0002t0002a0003c0003t0002others(1): Show | 43 | HG00423.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*336T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 22/22 | 4392 | chr1 | 182560449 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:182450489
|
T | C | 100 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0017others(97): Show | 102 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.13+311T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450489 | ||||||
| chr1:182450505
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0114others(73): Show | 80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.13+327T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450505 | ||||||
| chr1:182450734
|
A | C | 2 | a0001c0001t0001g0103a0003c0024t0001g0104 | 2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.13+556A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450734 | ||||||
| chr1:182450809
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13+631C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450809 | ||||||
| chr1:182450819
|
T | C | 4 | a0001c0004t0001g0105a0001c0004t0001g0107a0001c0005t0001g0108others(1): Show | 4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+641T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450819 | ||||||
| chr1:182450907
|
G | C | 3 | a0001c0001t0001g0181a0001c0004t0001g0180a0003c0003t0002g0179 | 3 | HG01891.hp2 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.13+729G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450907 | ||||||
| chr1:182451038
|
G | T | 4 | a0001c0005t0001g0327a0001c0005t0001g0330a0002c0002t0001g0328others(1): Show | 4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+860G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451038 | ||||||
| chr1:182451070
|
T | G | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.13+892T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451070 | ||||||
| chr1:182451087
|
A | T | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.13+909A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451087 | ||||||
| chr1:182451143
|
C | A | 1 | a0003c0003t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.13+965C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451143 | ||||||
| chr1:182451143
|
C | CA | 101 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0030others(98): Show | 103 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.13+984dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451143 | |||||
| chr1:182451143
|
C | CAA | 9 | a0001c0001t0001g0008a0001c0001t0001g0102a0001c0001t0001g0182others(6): Show | 9 | HG00423.hp1 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+983_13+984dupAA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451143 | |||||
| chr1:182451143
|
CA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0113a0001c0001t0001g0114others(74): Show | 81 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.13+984delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451143 | |||||
| chr1:182451209
|
A | T | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.13+1031A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451209 | ||||||
| chr1:182451258
|
A | G | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.13+1080A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451258 | ||||||
| chr1:182451283
|
G | A | 1 | a0001c0005t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.13+1105G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451283 | ||||||
| chr1:182451313
|
G | A | 248 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0014others(245): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.13+1135G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451313 | ||||||
| chr1:182451340
|
A | G | 1 | a0001c0004t0001g0321 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.13+1162A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451340 | ||||||
| chr1:182451356
|
A | T | 1 | a0002c0002t0001g0178 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.13+1178A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451356 | ||||||
| chr1:182451422
|
C | G | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.13+1244C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451422 | ||||||
| chr1:182451455
|
G | A | 3 | a0001c0007t0001g0194a0002c0002t0001g0195a0002c0002t0001g0196 | 3 | HG02622.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+1277G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451455 | ||||||
| chr1:182451475
|
G | GGATATAC others(102): Show |
30 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0296others(27): Show | 30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1297_13+1298ins others(109): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451475 | ||||||
| chr1:182451476
|
C | T | 30 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0296others(27): Show | 30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1298C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451476 | ||||||
| chr1:182451478
|
G | A | 30 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0296others(27): Show | 30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1300G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451478 | ||||||
| chr1:182451485
|
C | T | 3 | a0001c0007t0001g0194a0002c0002t0001g0195a0002c0002t0001g0196 | 3 | HG02622.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+1307C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451485 | ||||||
| chr1:182451499
|
T | A | 30 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0296others(27): Show | 30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1321T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451499 | ||||||
| chr1:182451505
|
A | G | 23 | a0001c0001t0001g0006a0001c0001t0001g0190a0001c0001t0001g0277others(20): Show | 24 | HG00423.hp2 HG01081.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.13+1327A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451505 | ||||||
| chr1:182451705
|
G | GGACATCA others(304): Show |
1 | a0002c0002t0001g0012 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.13+1544_13+1545ins others(311): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | |||||
| chr1:182451705
|
G | GGACATCA others(318): Show |
4 | a0001c0001t0001g0014a0001c0005t0001g0010a0003c0003t0002g0015others(1): Show | 4 | HG03225.hp2 HG03831.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(325): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | |||||
| chr1:182451705
|
G | GGACATCA others(319): Show |
30 | a0001c0001t0001g0017a0001c0001t0001g0030a0001c0001t0001g0043others(27): Show | 30 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(326): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | |||||
| chr1:182451705
|
G | GGACATCA others(319): Show |
1 | a0001c0004t0002g0044 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.13+1544_13+1545ins others(326): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | |||||
| chr1:182451705
|
G | GGACATCA others(320): Show |
50 | a0001c0001t0001g0008a0001c0001t0001g0048a0001c0001t0001g0052others(47): Show | 52 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(327): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | |||||
| chr1:182451705
|
G | GGACATCA others(321): Show |
8 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0004t0001g0009others(5): Show | 8 | HG00438.hp1 HG00741.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(328): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | |||||
| chr1:182451705
|
G | GGACATCA others(322): Show |
2 | a0002c0002t0001g0097a0002c0002t0001g0098 | 2 | HG00738.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(329): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | |||||
| chr1:182451705
|
G | GGACATCA others(323): Show |
1 | a0002c0002t0001g0099 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.13+1544_13+1545ins others(330): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | |||||
| chr1:182451776
|
G | A | 4 | a0001c0001t0001g0296a0001c0001t0001g0297a0003c0003t0001g0295others(1): Show | 4 | HG00438.hp2 NA18962.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+1598G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451776 | ||||||
| chr1:182451837
|
T | C | 4 | a0001c0005t0001g0327a0001c0005t0001g0330a0002c0002t0001g0328others(1): Show | 4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+1659T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451837 | ||||||
| chr1:182451923
|
G | A | 3 | a0001c0007t0001g0194a0002c0002t0001g0195a0002c0002t0001g0196 | 3 | HG02622.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+1745G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451923 | ||||||
| chr1:182452141
|
G | T | 1 | a0003c0003t0001g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.14-1817G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452141 | ||||||
| chr1:182452292
|
G | A | 1 | a0001c0004t0001g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14-1666G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452292 | ||||||
| chr1:182452518
|
T | C | 5 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG01069.hp1 HG02055.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-1440T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452518 | ||||||
| chr1:182452556
|
G | A | 5 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0004t0001g0183others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-1402G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452556 | ||||||
| chr1:182452657
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.14-1301T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452657 | ||||||
| chr1:182453037
|
T | C | 9 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0004t0001g0105others(6): Show | 9 | HG01346.hp2 HG02258.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.14-921T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453037 | ||||||
| chr1:182453052
|
A | G | 4 | a0001c0005t0001g0327a0001c0005t0001g0330a0002c0002t0001g0328others(1): Show | 4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-906A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453052 | ||||||
| chr1:182453532
|
G | A | 30 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0296others(27): Show | 30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.14-426G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453532 | ||||||
| chr1:182453565
|
G | A | 6 | a0002c0002t0001g0118a0002c0002t0001g0119a0002c0002t0001g0120others(3): Show | 6 | NA18941.hp2 NA18953.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-393G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453565 | ||||||
| chr1:182453877
|
T | C | 11 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0004t0001g0214others(8): Show | 11 | HG01891.hp1 HG02280.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.14-81T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453877 | ||||||
| chr1:182453888
|
G | C | 1 | a0003c0003t0001g0016 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.14-70G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453888 | ||||||
| chr1:182453920
|
T | G | 1 | a0003c0003t0002g0215 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.14-38T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453920 | ||||||
| chr1:182454076
|
C | T | 4 | a0001c0001t0001g0181a0001c0007t0001g0194a0002c0002t0001g0195others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+36C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454076 | ||||||
| chr1:182454077
|
A | G | 4 | a0001c0005t0001g0327a0001c0005t0001g0330a0002c0002t0001g0328others(1): Show | 4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+37A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454077 | ||||||
| chr1:182454100
|
A | C | 15 | a0001c0001t0001g0102a0001c0001t0001g0181a0001c0001t0001g0201others(12): Show | 15 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+60A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454100 | ||||||
| chr1:182454163
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.96+123A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454163 | ||||||
| chr1:182454164
|
T | TA | 15 | a0001c0001t0001g0102a0001c0001t0001g0181a0001c0001t0001g0201others(12): Show | 15 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+131dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454164 | |||||
| chr1:182454323
|
C | T | 9 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0004t0001g0180others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+283C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454323 | ||||||
| chr1:182454441
|
A | G | 31 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0296others(28): Show | 31 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+401A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454441 | ||||||
| chr1:182454446
|
C | T | 1 | a0001c0004t0001g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.96+406C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454446 | ||||||
| chr1:182454447
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.96+407G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454447 | ||||||
| chr1:182454524
|
C | A | 1 | a0003c0003t0002g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.96+484C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454524 | ||||||
| chr1:182454586
|
A | ATG | 5 | a0001c0001t0001g0043a0001c0001t0001g0103a0001c0005t0001g0268others(2): Show | 5 | HG00639.hp2 HG02148.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+585_96+586dupTG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | |||||
| chr1:182454586
|
A | ATGTG | 9 | a0001c0001t0001g0201a0001c0001t0001g0265a0001c0001t0001g0266others(6): Show | 9 | HG01258.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+583_96+586dupTG others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | |||||
| chr1:182454586
|
A | ATGTGTG | 3 | a0001c0004t0001g0187a0001c0004t0001g0188a0001c0004t0001g0189 | 3 | HG01109.hp1 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+581_96+586dupTG others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | |||||
| chr1:182454586
|
ATG | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0191a0001c0001t0001g0296others(29): Show | 32 | HG00438.hp2 HG00642.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.96+585_96+586delTG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | |||||
| chr1:182454586
|
ATGTG | A | 108 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0048others(105): Show | 110 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.96+583_96+586delTG others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | |||||
| chr1:182454586
|
ATGTGTG | A | 71 | a0001c0001t0001g0017a0001c0001t0001g0114a0001c0001t0001g0131others(68): Show | 73 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.96+581_96+586delTG others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | |||||
| chr1:182454586
|
ATGTGTGT others(1): Show |
A | 28 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0182others(25): Show | 31 | HG00423.hp2 HG01070.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+579_96+586delTG others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | |||||
| chr1:182454586
|
ATGTGTGT others(3): Show |
A | 11 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0181others(8): Show | 11 | HG01069.hp1 HG01346.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+577_96+586delTG others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | |||||
| chr1:182454586
|
ATGTGTGT others(5): Show |
A | 4 | a0001c0005t0001g0327a0001c0005t0001g0330a0002c0002t0001g0328others(1): Show | 4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+575_96+586delTG others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | |||||
| chr1:182454602
|
G | A | 10 | a0001c0001t0001g0102a0001c0001t0001g0113a0001c0001t0001g0181others(7): Show | 10 | HG01069.hp1 HG01346.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+562G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454602 | ||||||
| chr1:182454630
|
C | G | 2 | a0001c0004t0001g0188a0001c0004t0001g0189 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+590C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454630 | ||||||
| chr1:182454667
|
A | C | 16 | a0001c0004t0001g0180a0001c0005t0001g0327a0001c0005t0001g0330others(13): Show | 16 | HG01099.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+627A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454667 | ||||||
| chr1:182454753
|
A | G | 17 | a0001c0001t0001g0114a0001c0001t0001g0166a0001c0001t0001g0168others(14): Show | 17 | HG01123.hp2 HG01192.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.96+713A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454753 | ||||||
| chr1:182454887
|
C | G | 1 | a0001c0001t0001g0297 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.96+847C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454887 | ||||||
| chr1:182454901
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0200 | 2 | HG01069.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.96+861C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454901 | ||||||
| chr1:182454958
|
C | T | 6 | a0004c0009t0001g0225a0004c0012t0001g0222a0004c0012t0001g0326others(3): Show | 6 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+918C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454958 | ||||||
| chr1:182455350
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0090others(84): Show | 89 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.96+1310G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455350 | ||||||
| chr1:182455439
|
G | A | 1 | a0001c0005t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.96+1399G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455439 | ||||||
| chr1:182455479
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.96+1439G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455479 | ||||||
| chr1:182455591
|
G | A | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.96+1551G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455591 | ||||||
| chr1:182455591
|
GA | G | 116 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0081others(113): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.96+1562delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182455591 | |||||
| chr1:182455591
|
GAA | G | 45 | a0001c0001t0001g0048a0001c0001t0001g0083a0001c0001t0001g0090others(42): Show | 46 | HG00280.hp2 HG00558.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+1561_96+1562del others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182455591 | |||||
| chr1:182455592
|
A | G | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.96+1552A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455592 | ||||||
| chr1:182455612
|
T | C | 5 | a0001c0001t0001g0102a0001c0001t0001g0140a0001c0001t0001g0199others(2): Show | 5 | HG02055.hp1 HG02055.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1572T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455612 | ||||||
| chr1:182455799
|
G | A | 1 | a0003c0003t0002g0132 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.96+1759G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455799 | ||||||
| chr1:182455850
|
C | T | 128 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0030others(125): Show | 131 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.96+1810C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455850 | ||||||
| chr1:182455912
|
C | T | 301 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0014others(298): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.96+1872C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455912 | ||||||
| chr1:182455946
|
G | A | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.96+1906G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455946 | ||||||
| chr1:182455959
|
C | T | 3 | a0001c0004t0001g0038a0001c0004t0001g0107a0001c0004t0001g0217 | 3 | HG02451.hp2 HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.96+1919C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455959 | ||||||
| chr1:182455980
|
G | A | 2 | a0001c0007t0001g0021a0001c0007t0001g0022 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.96+1940G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455980 | ||||||
| chr1:182456063
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0056others(25): Show | 28 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.96+2023G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456063 | ||||||
| chr1:182456063
|
G | T | 1 | a0002c0002t0001g0011 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.96+2023G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456063 | ||||||
| chr1:182456221
|
C | T | 158 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0014others(155): Show | 164 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.97-2098C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456221 | ||||||
| chr1:182456299
|
C | CT | 63 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(60): Show | 64 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.97-2005dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182456299 | |||||
| chr1:182456539
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.97-1780C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456539 | ||||||
| chr1:182456564
|
C | T | 1 | a0003c0003t0002g0005 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.97-1755C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456564 | ||||||
| chr1:182456582
|
G | A | 1 | a0001c0007t0001g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-1737G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456582 | ||||||
| chr1:182456617
|
C | T | 2 | a0001c0004t0001g0279a0002c0002t0002g0288 | 2 | HG01169.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.97-1702C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456617 | ||||||
| chr1:182456651
|
A | T | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.97-1668A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456651 | ||||||
| chr1:182456839
|
G | A | 2 | a0003c0003t0002g0018a0003c0003t0002g0215 | 2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.97-1480G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456839 | ||||||
| chr1:182456912
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.97-1407C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456912 | ||||||
| chr1:182456913
|
G | A | 1 | a0003c0003t0002g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.97-1406G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456913 | ||||||
| chr1:182456934
|
G | T | 99 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0052others(96): Show | 99 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.97-1385G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456934 | ||||||
| chr1:182456994
|
A | T | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.97-1325A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456994 | ||||||
| chr1:182457148
|
A | AAAAC | 131 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(128): Show | 132 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.97-1155_97-1152dup others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182457148 | |||||
| chr1:182457177
|
T | C | 1 | a0001c0004t0001g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.97-1142T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457177 | ||||||
| chr1:182457230
|
G | C | 4 | a0001c0001t0001g0201a0001c0001t0001g0272a0001c0001t0001g0273others(1): Show | 4 | HG02145.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-1089G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457230 | ||||||
| chr1:182457336
|
A | G | 1 | a0009c0011t0001g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-983A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457336 | ||||||
| chr1:182457400
|
G | T | 11 | a0001c0001t0001g0103a0001c0001t0001g0181a0001c0001t0001g0184others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-919G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457400 | ||||||
| chr1:182457462
|
C | A | 126 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(123): Show | 127 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.97-857C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457462 | ||||||
| chr1:182457487
|
T | A | 1 | a0002c0002t0001g0109 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.97-832T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457487 | ||||||
| chr1:182457532
|
G | T | 1 | a0003c0003t0001g0156 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.97-787G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457532 | ||||||
| chr1:182457570
|
G | A | 130 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(127): Show | 131 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.97-749G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457570 | ||||||
| chr1:182457682
|
G | A | 2 | a0001c0001t0001g0181a0014c0019t0001g0228 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.97-637G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457682 | ||||||
| chr1:182457693
|
G | A | 7 | a0001c0001t0001g0218a0001c0006t0001g0173a0001c0006t0001g0174others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-626G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457693 | ||||||
| chr1:182457762
|
G | T | 142 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(139): Show | 143 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.97-557G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457762 | ||||||
| chr1:182458097
|
G | A | 2 | a0002c0002t0001g0094a0002c0002t0001g0097 | 2 | NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.97-222G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182458097 | ||||||
| chr1:182458220
|
G | A | 51 | a0001c0001t0001g0052a0001c0001t0001g0133a0001c0001t0001g0142others(48): Show | 51 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.97-99G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182458220 | ||||||
| chr1:182458524
|
C | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0017others(124): Show | 128 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.171+131C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182458524 | ||||||
| chr1:182458627
|
G | A | 66 | a0001c0001t0001g0052a0001c0001t0001g0103a0001c0001t0001g0133others(63): Show | 66 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.171+234G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182458627 | ||||||
| chr1:182458857
|
G | A | 1 | a0003c0003t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.171+464G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182458857 | ||||||
| chr1:182459205
|
A | C | 1 | a0001c0001t0001g0311 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.172-799A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459205 | ||||||
| chr1:182459470
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.172-534G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459470 | ||||||
| chr1:182459578
|
A | G | 2 | a0001c0007t0001g0021a0001c0007t0001g0022 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.172-426A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459578 | ||||||
| chr1:182459657
|
A | G | 2 | a0001c0001t0001g0296a0007c0018t0001g0298 | 2 | NA18962.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.172-347A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459657 | ||||||
| chr1:182459659
|
C | A | 1 | a0001c0005t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.172-345C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459659 | ||||||
| chr1:182459704
|
G | A | 3 | a0001c0001t0001g0218a0003c0003t0001g0117a0017c0014t0001g0167 | 3 | HG01884.hp2 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.172-300G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459704 | ||||||
| chr1:182459749
|
G | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0001t0001g0199others(8): Show | 11 | HG01069.hp1 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.172-255G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459749 | ||||||
| chr1:182459892
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.172-112T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459892 | ||||||
| chr1:182459945
|
A | AT | 4 | a0001c0006t0001g0173a0001c0006t0001g0174a0002c0002t0001g0195others(1): Show | 4 | HG02559.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-52dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 182459945 | |||||
| chr1:182460160
|
C | CTGTG | 3 | a0001c0001t0001g0017a0001c0001t0001g0141a0001c0001t0001g0253 | 3 | HG02040.hp2 HG02155.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.301+49_301+52dupGT others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460160 | |||||
| chr1:182460160
|
CTG | C | 209 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0030others(206): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.301+51_301+52delGT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460160 | |||||
| chr1:182460160
|
CTGTG | C | 5 | a0001c0001t0001g0083a0001c0001t0001g0113a0001c0001t0001g0140others(2): Show | 5 | HG00735.hp2 HG01069.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+49_301+52delGT others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460160 | |||||
| chr1:182460164
|
GTGTGTGT others(57): Show |
G | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.301+51_301+114delG others(63): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460164 | |||||
| chr1:182460166
|
GTGTGTGT others(55): Show |
G | 1 | a0001c0004t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.301+81_301+142delA others(61): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460166 | |||||
| chr1:182460184
|
G | GTGTA | 7 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(4): Show | 7 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+52_301+53insGT others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460184 | |||||
| chr1:182460184
|
G | GTGTGTA | 4 | a0001c0001t0001g0181a0009c0011t0001g0185a0009c0011t0001g0186others(1): Show | 4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+52_301+53insGT others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460184 | |||||
| chr1:182460226
|
GTA | G | 11 | a0001c0001t0001g0103a0001c0001t0001g0181a0001c0001t0001g0184others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.301+95_301+96delAT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460226 | |||||
| chr1:182460228
|
A | ATG | 3 | a0001c0001t0001g0048a0001c0004t0001g0252a0003c0003t0001g0089 | 3 | HG03927.hp1 NA19091.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.301+113_301+114dup others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460228 | |||||
| chr1:182460228
|
A | T | 3 | a0001c0001t0001g0218a0003c0003t0001g0117a0017c0014t0001g0167 | 3 | HG01884.hp2 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.301+95A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460228 | ||||||
| chr1:182460240
|
G | A | 32 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0056others(29): Show | 32 | HG00438.hp2 HG00673.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.301+107G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460240 | ||||||
| chr1:182460338
|
A | G | 1 | a0002c0002t0001g0079 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.301+205A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460338 | ||||||
| chr1:182460398
|
G | T | 1 | a0002c0002t0001g0078 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.301+265G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460398 | ||||||
| chr1:182460437
|
A | G | 2 | a0002c0002t0001g0195a0002c0002t0001g0196 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.301+304A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460437 | ||||||
| chr1:182460439
|
T | C | 5 | a0001c0001t0001g0191a0001c0001t0001g0301a0001c0001t0001g0302others(2): Show | 5 | NA18977.hp2 NA19000.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+306T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460439 | ||||||
| chr1:182460470
|
C | A | 34 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0056others(31): Show | 34 | HG00438.hp2 HG00673.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.301+337C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460470 | ||||||
| chr1:182460593
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(273): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.301+460T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460593 | ||||||
| chr1:182460650
|
A | G | 5 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0075others(2): Show | 7 | NA18951.hp1 NA18970.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+517A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460650 | ||||||
| chr1:182460752
|
A | G | 1 | a0002c0002t0001g0260 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.301+619A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460752 | ||||||
| chr1:182460807
|
G | A | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.301+674G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460807 | ||||||
| chr1:182460860
|
C | A | 43 | a0001c0001t0001g0048a0001c0001t0001g0052a0001c0001t0001g0081others(40): Show | 43 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.301+727C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460860 | ||||||
| chr1:182460920
|
G | C | 2 | a0004c0012t0001g0222a0004c0012t0001g0326 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.301+787G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460920 | ||||||
| chr1:182460941
|
G | C | 1 | a0001c0004t0001g0082 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.301+808G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460941 | ||||||
| chr1:182460992
|
T | C | 1 | a0003c0003t0002g0132 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.301+859T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460992 | ||||||
| chr1:182461026
|
G | A | 2 | a0001c0004t0001g0231a0001c0004t0001g0232 | 2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.301+893G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461026 | ||||||
| chr1:182461103
|
A | G | 67 | a0001c0004t0001g0111a0001c0004t0001g0129a0003c0003t0001g0029others(64): Show | 69 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.301+970A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461103 | ||||||
| chr1:182461136
|
C | CT | 67 | a0001c0004t0001g0111a0001c0004t0001g0129a0003c0003t0001g0029others(64): Show | 69 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.301+1013dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182461136 | |||||
| chr1:182461200
|
T | A | 1 | a0001c0001t0001g0008 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.301+1067T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461200 | ||||||
| chr1:182461313
|
G | GTAA | 73 | a0001c0001t0001g0140a0001c0001t0001g0200a0001c0001t0001g0216others(70): Show | 76 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.301+1199_301+1201d others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182461313 | |||||
| chr1:182461313
|
G | GTAATAA | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0003c0003t0001g0029others(3): Show | 6 | HG02809.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+1196_301+1201d others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182461313 | |||||
| chr1:182461359
|
A | C | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301+1226A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461359 | ||||||
| chr1:182461366
|
C | A | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.301+1233C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461366 | ||||||
| chr1:182461395
|
G | A | 70 | a0001c0004t0001g0111a0001c0004t0001g0129a0003c0003t0001g0029others(67): Show | 73 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.301+1262G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461395 | ||||||
| chr1:182461544
|
T | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 48 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.301+1411T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461544 | ||||||
| chr1:182461581
|
A | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0268 | 3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.301+1448A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461581 | ||||||
| chr1:182461585
|
T | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+1452T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461585 | ||||||
| chr1:182461663
|
A | G | 7 | a0001c0001t0001g0113a0001c0001t0001g0181a0001c0001t0001g0216others(4): Show | 8 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+1530A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461663 | ||||||
| chr1:182461780
|
ATAGGACA others(8): Show |
A | 101 | a0001c0001t0001g0274a0001c0004t0001g0038a0001c0004t0001g0082others(98): Show | 103 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.301+1650_301+1664d others(17): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182461780 | |||||
| chr1:182461783
|
G | A | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.301+1650G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461783 | ||||||
| chr1:182461896
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+1763A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461896 | ||||||
| chr1:182461962
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.301+1829G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461962 | ||||||
| chr1:182461963
|
G | T | 66 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(63): Show | 69 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.301+1830G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461963 | ||||||
| chr1:182462030
|
T | G | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+1897T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462030 | ||||||
| chr1:182462073
|
T | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+1940T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462073 | ||||||
| chr1:182462182
|
T | G | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+2049T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462182 | ||||||
| chr1:182462309
|
A | G | 1 | a0001c0001t0001g0250 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.301+2176A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462309 | ||||||
| chr1:182462459
|
T | G | 1 | a0001c0005t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.301+2326T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462459 | ||||||
| chr1:182462560
|
G | A | 12 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(9): Show | 12 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+2427G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462560 | ||||||
| chr1:182462578
|
A | T | 71 | a0001c0004t0001g0111a0001c0004t0001g0129a0003c0003t0001g0016others(68): Show | 74 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.301+2445A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462578 | ||||||
| chr1:182463029
|
C | T | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+2896C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463029 | ||||||
| chr1:182463046
|
A | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(316): Show | 327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.301+2913A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463046 | ||||||
| chr1:182463064
|
C | T | 5 | a0001c0004t0001g0009a0001c0004t0001g0257a0001c0004t0001g0286others(2): Show | 5 | HG00735.hp1 HG01255.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+2931C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463064 | ||||||
| chr1:182463110
|
G | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+2977G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463110 | ||||||
| chr1:182463118
|
C | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(40): Show | 45 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.301+2985C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463118 | ||||||
| chr1:182463167
|
G | A | 1 | a0001c0004t0001g0180 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.301+3034G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463167 | ||||||
| chr1:182463183
|
A | C | 4 | a0003c0003t0001g0051a0003c0003t0001g0154a0003c0003t0001g0155others(1): Show | 4 | NA18951.hp2 NA18952.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+3050A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463183 | ||||||
| chr1:182463193
|
T | C | 1 | a0002c0002t0001g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.301+3060T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463193 | ||||||
| chr1:182463272
|
C | T | 2 | a0003c0003t0001g0115a0003c0003t0002g0015 | 2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.301+3139C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463272 | ||||||
| chr1:182463293
|
C | CA | 54 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(51): Show | 56 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.301+3178dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182463293 | |||||
| chr1:182463359
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.301+3226C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463359 | ||||||
| chr1:182463472
|
A | G | 2 | a0001c0004t0001g0231a0001c0004t0001g0232 | 2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.301+3339A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463472 | ||||||
| chr1:182463515
|
A | G | 2 | a0001c0001t0001g0181a0014c0019t0001g0228 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.301+3382A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463515 | ||||||
| chr1:182463551
|
T | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0274 | 2 | NA18944.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.301+3418T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463551 | ||||||
| chr1:182463680
|
T | G | 3 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0268 | 3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.301+3547T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463680 | ||||||
| chr1:182463749
|
A | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.301+3616A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463749 | ||||||
| chr1:182464259
|
T | C | 8 | a0001c0001t0001g0274a0001c0004t0001g0082a0001c0004t0001g0124others(5): Show | 8 | HG02071.hp1 NA18947.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+4126T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464259 | ||||||
| chr1:182464365
|
T | C | 1 | a0002c0002t0001g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.301+4232T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464365 | ||||||
| chr1:182464462
|
G | A | 1 | a0002c0002t0001g0075 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.301+4329G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464462 | ||||||
| chr1:182464727
|
G | GA | 10 | a0001c0001t0001g0081a0001c0001t0001g0238a0001c0001t0001g0239others(7): Show | 10 | HG00738.hp1 HG01243.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.301+4607dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182464727 | |||||
| chr1:182464761
|
T | C | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.301+4628T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464761 | ||||||
| chr1:182464852
|
T | C | 71 | a0001c0004t0001g0111a0001c0004t0001g0129a0003c0003t0001g0016others(68): Show | 74 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.301+4719T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464852 | ||||||
| chr1:182464854
|
G | C | 1 | a0001c0005t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.301+4721G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464854 | ||||||
| chr1:182464916
|
G | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(33): Show | 38 | HG00673.hp2 HG00735.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.301+4783G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464916 | ||||||
| chr1:182465082
|
A | AATAATAA others(215): Show |
1 | a0001c0005t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301+4961_301+4962i others(224): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | |||||
| chr1:182465082
|
A | AATAATAA others(213): Show |
2 | a0001c0001t0001g0200a0001c0001t0001g0216 | 2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.301+4961_301+4962i others(222): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | |||||
| chr1:182465082
|
A | AATAATAA others(211): Show |
2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.301+4961_301+4962i others(220): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | |||||
| chr1:182465082
|
A | AATAATAA others(219): Show |
2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.301+4961_301+4962i others(228): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | |||||
| chr1:182465082
|
A | AATAATAA others(211): Show |
1 | a0001c0001t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.301+4961_301+4962i others(220): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | |||||
| chr1:182465100
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+4967A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465100 | ||||||
| chr1:182465190
|
T | C | 1 | a0003c0003t0001g0145 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.301+5057T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465190 | ||||||
| chr1:182465196
|
AGATAGAA others(1): Show |
A | 8 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(5): Show | 8 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+5067_301+5074d others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465196 | |||||
| chr1:182465351
|
A | G | 69 | a0001c0004t0001g0111a0001c0004t0001g0129a0003c0003t0001g0016others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.301+5218A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465351 | ||||||
| chr1:182465380
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(32): Show | 37 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.301+5247G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465380 | ||||||
| chr1:182465469
|
G | C | 9 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+5336G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465469 | ||||||
| chr1:182465470
|
G | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+5337G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465470 | ||||||
| chr1:182465606
|
T | TATA | 2 | a0002c0002t0001g0004a0002c0002t0001g0076 | 3 | NA18977.hp1 NA19011.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.301+5487_301+5489d others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465606 | |||||
| chr1:182465647
|
C | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(42): Show | 47 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.301+5514C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465647 | ||||||
| chr1:182465702
|
G | A | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.301+5569G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465702 | ||||||
| chr1:182465870
|
G | C | 1 | a0002c0002t0001g0118 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.301+5737G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465870 | ||||||
| chr1:182466039
|
C | T | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.301+5906C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466039 | ||||||
| chr1:182466103
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.301+5970A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466103 | ||||||
| chr1:182466123
|
GA | G | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.301+5999delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182466123 | |||||
| chr1:182466217
|
A | G | 3 | a0001c0006t0001g0208a0001c0006t0001g0209a0001c0006t0001g0210 | 3 | HG01891.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.301+6084A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466217 | ||||||
| chr1:182466539
|
G | C | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-5857G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466539 | ||||||
| chr1:182466577
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.302-5819A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466577 | ||||||
| chr1:182466586
|
C | T | 1 | a0003c0003t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.302-5810C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466586 | ||||||
| chr1:182466603
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.302-5793T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466603 | ||||||
| chr1:182466621
|
A | G | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.302-5775A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466621 | ||||||
| chr1:182466649
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.302-5747C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466649 | ||||||
| chr1:182466749
|
A | C | 9 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-5647A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466749 | ||||||
| chr1:182466821
|
T | C | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-5575T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466821 | ||||||
| chr1:182466874
|
T | A | 1 | a0002c0002t0001g0275 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.302-5522T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466874 | ||||||
| chr1:182466879
|
A | G | 25 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0040others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.302-5517A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466879 | ||||||
| chr1:182466945
|
T | C | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-5451T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466945 | ||||||
| chr1:182467021
|
T | C | 1 | a0011c0023t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-5375T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467021 | ||||||
| chr1:182467023
|
C | A | 1 | a0011c0023t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-5373C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467023 | ||||||
| chr1:182467056
|
C | A | 43 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(40): Show | 45 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.302-5340C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467056 | ||||||
| chr1:182467103
|
A | G | 1 | a0001c0001t0001g0063 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.302-5293A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467103 | ||||||
| chr1:182467135
|
G | T | 1 | a0001c0004t0001g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.302-5261G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467135 | ||||||
| chr1:182467268
|
T | C | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.302-5128T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467268 | ||||||
| chr1:182467304
|
C | T | 40 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(37): Show | 41 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.302-5092C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467304 | ||||||
| chr1:182467427
|
C | T | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-4969C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467427 | ||||||
| chr1:182467431
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(132): Show | 140 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-4965C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467431 | ||||||
| chr1:182467441
|
C | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.302-4955C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467441 | ||||||
| chr1:182467584
|
G | T | 68 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(65): Show | 71 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.302-4812G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467584 | ||||||
| chr1:182467647
|
C | T | 1 | a0002c0002t0001g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.302-4749C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467647 | ||||||
| chr1:182467746
|
T | C | 1 | a0003c0003t0002g0132 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.302-4650T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467746 | ||||||
| chr1:182467844
|
A | G | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-4552A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467844 | ||||||
| chr1:182467904
|
C | A | 3 | a0002c0002t0001g0106a0006c0013t0001g0223a0006c0013t0001g0224 | 3 | HG02109.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.302-4492C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467904 | ||||||
| chr1:182467961
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.302-4435A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467961 | ||||||
| chr1:182468071
|
A | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(141): Show | 149 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.302-4325A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468071 | ||||||
| chr1:182468094
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.302-4302C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468094 | ||||||
| chr1:182468095
|
G | A | 1 | a0001c0001t0001g0309 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.302-4301G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468095 | ||||||
| chr1:182468193
|
G | T | 1 | a0003c0003t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.302-4203G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468193 | ||||||
| chr1:182468275
|
T | C | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-4121T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468275 | ||||||
| chr1:182468307
|
C | T | 1 | a0002c0002t0001g0011 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.302-4089C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468307 | ||||||
| chr1:182468333
|
C | T | 28 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0040others(25): Show | 28 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.302-4063C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468333 | ||||||
| chr1:182468374
|
C | T | 1 | a0001c0005t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.302-4022C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468374 | ||||||
| chr1:182468422
|
G | A | 1 | a0011c0023t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-3974G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468422 | ||||||
| chr1:182468424
|
A | T | 1 | a0011c0023t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-3972A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468424 | ||||||
| chr1:182468425
|
T | A | 1 | a0011c0023t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-3971T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468425 | ||||||
| chr1:182468488
|
A | G | 1 | a0004c0009t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.302-3908A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468488 | ||||||
| chr1:182468778
|
T | A | 3 | a0001c0001t0001g0190a0001c0001t0001g0261a0001c0001t0001g0294 | 3 | HG01978.hp1 HG02738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.302-3618T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468778 | ||||||
| chr1:182468780
|
A | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0261a0001c0001t0001g0294 | 3 | HG01978.hp1 HG02738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.302-3616A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468780 | ||||||
| chr1:182468808
|
G | T | 1 | a0011c0023t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-3588G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468808 | ||||||
| chr1:182468835
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(132): Show | 140 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-3561A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468835 | ||||||
| chr1:182468968
|
G | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(132): Show | 140 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-3428G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468968 | ||||||
| chr1:182468971
|
C | T | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.302-3425C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468971 | ||||||
| chr1:182469001
|
A | T | 1 | a0003c0003t0002g0251 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.302-3395A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469001 | ||||||
| chr1:182469032
|
G | A | 3 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0268 | 3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.302-3364G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469032 | ||||||
| chr1:182469367
|
C | A | 37 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(34): Show | 38 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.302-3029C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469367 | ||||||
| chr1:182469404
|
C | A | 2 | a0001c0004t0001g0170a0001c0004t0001g0270 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.302-2992C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469404 | ||||||
| chr1:182469422
|
G | A | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-2974G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469422 | ||||||
| chr1:182469436
|
G | A | 1 | a0002c0002t0001g0219 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.302-2960G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469436 | ||||||
| chr1:182469511
|
G | A | 68 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(65): Show | 71 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.302-2885G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469511 | ||||||
| chr1:182469519
|
G | T | 1 | a0015c0021t0001g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.302-2877G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469519 | ||||||
| chr1:182469577
|
A | T | 9 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-2819A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469577 | ||||||
| chr1:182469593
|
T | C | 2 | a0001c0004t0001g0314a0001c0004t0001g0315 | 2 | HG00642.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.302-2803T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469593 | ||||||
| chr1:182469604
|
C | T | 1 | a0008c0010t0001g0206 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.302-2792C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469604 | ||||||
| chr1:182469675
|
G | A | 1 | a0003c0003t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.302-2721G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469675 | ||||||
| chr1:182469895
|
A | C | 2 | a0001c0001t0001g0056a0001c0001t0001g0093 | 2 | NA18982.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.302-2501A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469895 | ||||||
| chr1:182469951
|
A | G | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.302-2445A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469951 | ||||||
| chr1:182470007
|
G | C | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.302-2389G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470007 | ||||||
| chr1:182470017
|
GGCAGTGA others(2): Show |
G | 3 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0268 | 3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.302-2377_302-2369d others(11): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182470017 | |||||
| chr1:182470018
|
G | A | 18 | a0002c0002t0001g0032a0002c0002t0001g0041a0002c0002t0001g0045others(15): Show | 18 | HG00438.hp1 HG01928.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.302-2378G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470018 | ||||||
| chr1:182470124
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.302-2272A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470124 | ||||||
| chr1:182470132
|
G | A | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-2264G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470132 | ||||||
| chr1:182470161
|
C | T | 10 | a0001c0001t0001g0081a0001c0001t0001g0216a0001c0001t0001g0238others(7): Show | 10 | HG00738.hp1 HG01243.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.302-2235C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470161 | ||||||
| chr1:182470228
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.302-2168C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470228 | ||||||
| chr1:182470266
|
A | G | 3 | a0001c0007t0001g0021a0001c0007t0001g0022a0001c0007t0001g0212 | 3 | HG02965.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.302-2130A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470266 | ||||||
| chr1:182470398
|
C | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(34): Show | 38 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.302-1998C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470398 | ||||||
| chr1:182470407
|
T | G | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.302-1989T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470407 | ||||||
| chr1:182470496
|
CG | C | 3 | a0003c0003t0001g0062a0003c0003t0001g0153a0003c0003t0001g0292 | 3 | HG00544.hp2 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.302-1899delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470496 | ||||||
| chr1:182470658
|
T | C | 1 | a0002c0002t0001g0195 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.302-1738T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470658 | ||||||
| chr1:182470690
|
T | C | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-1706T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470690 | ||||||
| chr1:182470786
|
T | C | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-1610T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470786 | ||||||
| chr1:182471172
|
A | G | 2 | a0002c0002t0001g0195a0002c0002t0001g0196 | 2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.302-1224A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471172 | ||||||
| chr1:182471311
|
C | A | 1 | a0011c0023t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-1085C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471311 | ||||||
| chr1:182471338
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.302-1058G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471338 | ||||||
| chr1:182471580
|
C | T | 7 | a0001c0004t0001g0100a0001c0004t0001g0105a0001c0004t0001g0183others(4): Show | 7 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.302-816C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471580 | ||||||
| chr1:182471619
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(112): Show | 120 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.302-777T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471619 | ||||||
| chr1:182471719
|
C | G | 1 | a0002c0002t0001g0289 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.302-677C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471719 | ||||||
| chr1:182471728
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.302-668C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471728 | ||||||
| chr1:182471788
|
G | C | 4 | a0002c0002t0001g0135a0002c0002t0001g0136a0002c0002t0001g0137others(1): Show | 4 | NA18978.hp2 NA19011.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-608G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471788 | ||||||
| chr1:182471865
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.302-531C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471865 | ||||||
| chr1:182471912
|
G | T | 4 | a0003c0003t0001g0051a0003c0003t0001g0154a0003c0003t0001g0155others(1): Show | 4 | NA18951.hp2 NA18952.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-484G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471912 | ||||||
| chr1:182471954
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.302-442C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471954 | ||||||
| chr1:182471970
|
C | A | 8 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(5): Show | 8 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-426C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471970 | ||||||
| chr1:182472063
|
G | GT | 71 | a0002c0002t0001g0196a0003c0003t0001g0016a0003c0003t0001g0029others(68): Show | 74 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.302-326dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182472063 | |||||
| chr1:182472140
|
C | T | 1 | a0003c0003t0002g0264 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.302-256C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182472140 | ||||||
| chr1:182472232
|
C | T | 9 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-164C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182472232 | ||||||
| chr1:182472311
|
G | A | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-85G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182472311 | ||||||
| chr1:182472676
|
A | G | 1 | a0002c0002t0001g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.463+119A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182472676 | ||||||
| chr1:182472700
|
C | A | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.463+143C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182472700 | ||||||
| chr1:182472797
|
C | G | 43 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(40): Show | 45 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.463+240C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182472797 | ||||||
| chr1:182473066
|
G | C | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.463+509G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182473066 | ||||||
| chr1:182473128
|
G | T | 1 | a0002c0002t0001g0118 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.464-447G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182473128 | ||||||
| chr1:182473375
|
T | C | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0005t0001g0010 | 3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.464-200T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182473375 | ||||||
| chr1:182474625
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1431+83G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182474625 | ||||||
| chr1:182475076
|
A | G | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1431+534A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475076 | ||||||
| chr1:182475435
|
T | C | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1431+893T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475435 | ||||||
| chr1:182475439
|
T | C | 1 | a0001c0004t0001g0128 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1431+897T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475439 | ||||||
| chr1:182475491
|
G | T | 1 | a0001c0004t0001g0125 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1431+949G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475491 | ||||||
| chr1:182475610
|
G | A | 1 | a0003c0003t0002g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1431+1068G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475610 | ||||||
| chr1:182475695
|
CCATCTCC others(13): Show |
C | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(33): Show | 38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1431+1159_1431+117 others(24): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182475695 | |||||
| chr1:182475867
|
C | T | 2 | a0003c0003t0001g0050a0003c0003t0001g0295 | 2 | NA18954.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1431+1325C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475867 | ||||||
| chr1:182475869
|
T | A | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1431+1327T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475869 | ||||||
| chr1:182476153
|
C | G | 4 | a0001c0001t0001g0113a0001c0001t0001g0181a0002c0002t0001g0079others(1): Show | 4 | HG01243.hp2 HG01346.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1431+1611C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476153 | ||||||
| chr1:182476377
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1431+1835A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476377 | ||||||
| chr1:182476394
|
C | T | 9 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1431+1852C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476394 | ||||||
| chr1:182476762
|
C | T | 1 | a0001c0004t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1431+2220C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476762 | ||||||
| chr1:182476962
|
C | A | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1431+2420C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476962 | ||||||
| chr1:182477053
|
G | T | 33 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(30): Show | 34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1431+2511G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477053 | ||||||
| chr1:182477059
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1431+2517G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477059 | ||||||
| chr1:182477080
|
C | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(37): Show | 42 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1431+2538C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477080 | ||||||
| chr1:182477221
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(177): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1431+2679G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477221 | ||||||
| chr1:182477361
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(177): Show | 186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1431+2819A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477361 | ||||||
| chr1:182477383
|
T | C | 3 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0268 | 3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1431+2841T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477383 | ||||||
| chr1:182477390
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1431+2848G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477390 | ||||||
| chr1:182477446
|
T | C | 69 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(66): Show | 72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1431+2904T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477446 | ||||||
| chr1:182477448
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1431+2906G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477448 | ||||||
| chr1:182477743
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1431+3201C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477743 | ||||||
| chr1:182477883
|
G | A | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+3341G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477883 | ||||||
| chr1:182477975
|
C | A | 2 | a0001c0004t0001g0180a0004c0009t0001g0225 | 2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1431+3433C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477975 | ||||||
| chr1:182478039
|
A | T | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+3497A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478039 | ||||||
| chr1:182478125
|
C | G | 1 | a0003c0003t0002g0310 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1431+3583C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478125 | ||||||
| chr1:182478125
|
C | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(8): Show | 11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1431+3583C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478125 | ||||||
| chr1:182478319
|
C | A | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+3777C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478319 | ||||||
| chr1:182478653
|
A | G | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1431+4111A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478653 | ||||||
| chr1:182478708
|
A | G | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1431+4166A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478708 | ||||||
| chr1:182478877
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(110): Show | 118 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1431+4335G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478877 | ||||||
| chr1:182478932
|
A | G | 2 | a0003c0003t0001g0117a0017c0014t0001g0167 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1431+4390A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478932 | ||||||
| chr1:182479023
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1431+4481A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479023 | ||||||
| chr1:182479056
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1431+4514G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479056 | ||||||
| chr1:182479146
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(127): Show | 135 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1431+4604G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479146 | ||||||
| chr1:182479566
|
C | T | 1 | a0002c0002t0001g0313 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1431+5024C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479566 | ||||||
| chr1:182479667
|
C | T | 10 | a0001c0004t0001g0092a0001c0004t0001g0284a0001c0004t0001g0285others(7): Show | 10 | HG00423.hp2 NA18941.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1431+5125C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479667 | ||||||
| chr1:182479768
|
G | A | 1 | a0001c0007t0001g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1431+5226G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479768 | ||||||
| chr1:182480080
|
A | G | 1 | a0002c0002t0001g0095 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1431+5538A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480080 | ||||||
| chr1:182480114
|
G | T | 1 | a0001c0004t0001g0009 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1431+5572G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480114 | ||||||
| chr1:182480207
|
C | T | 1 | a0004c0009t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1431+5665C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480207 | ||||||
| chr1:182480285
|
G | T | 65 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(62): Show | 68 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1431+5743G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480285 | ||||||
| chr1:182480460
|
G | GT | 70 | a0001c0001t0001g0218a0001c0001t0001g0273a0003c0003t0001g0016others(67): Show | 73 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1431+5933dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182480460 | |||||
| chr1:182480486
|
C | T | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1431+5944C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480486 | ||||||
| chr1:182480516
|
C | T | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+5974C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480516 | ||||||
| chr1:182480646
|
G | T | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+6104G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480646 | ||||||
| chr1:182481210
|
TA | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(111): Show | 119 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1431+6676delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182481210 | |||||
| chr1:182481241
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1431+6699A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481241 | ||||||
| chr1:182481487
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-6798C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481487 | ||||||
| chr1:182481488
|
G | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(30): Show | 34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1432-6797G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481488 | ||||||
| chr1:182481715
|
G | C | 6 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(3): Show | 6 | HG01069.hp1 HG02055.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432-6570G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481715 | ||||||
| chr1:182481742
|
C | T | 1 | a0003c0003t0001g0047 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1432-6543C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481742 | ||||||
| chr1:182481754
|
G | GGGA | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(178): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1432-6530_1432-652 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182481754 | |||||
| chr1:182481930
|
G | A | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1432-6355G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481930 | ||||||
| chr1:182482355
|
A | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(316): Show | 327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.1432-5930A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482355 | ||||||
| chr1:182482390
|
T | C | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1432-5895T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482390 | ||||||
| chr1:182482410
|
T | TA | 38 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(35): Show | 39 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1432-5867dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182482410 | |||||
| chr1:182482551
|
G | A | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-5734G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482551 | ||||||
| chr1:182482681
|
T | C | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-5604T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482681 | ||||||
| chr1:182482704
|
A | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-5581A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482704 | ||||||
| chr1:182482886
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(111): Show | 119 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1432-5399G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482886 | ||||||
| chr1:182483103
|
C | A | 1 | a0001c0006t0001g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1432-5182C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483103 | ||||||
| chr1:182483152
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1432-5133G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483152 | ||||||
| chr1:182483194
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(128): Show | 136 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1432-5091G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483194 | ||||||
| chr1:182483227
|
G | A | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-5058G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483227 | ||||||
| chr1:182483371
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-4914A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483371 | ||||||
| chr1:182483501
|
A | G | 1 | a0001c0004t0001g0283 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1432-4784A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483501 | ||||||
| chr1:182483548
|
A | G | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-4737A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483548 | ||||||
| chr1:182483551
|
C | T | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432-4734C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483551 | ||||||
| chr1:182483694
|
A | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0141a0001c0001t0001g0253 | 3 | HG02040.hp2 HG02155.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1432-4591A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483694 | ||||||
| chr1:182483702
|
T | C | 1 | a0001c0001t0001g0305 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1432-4583T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483702 | ||||||
| chr1:182483768
|
G | A | 1 | a0001c0005t0001g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1432-4517G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483768 | ||||||
| chr1:182483978
|
G | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(44): Show | 49 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1432-4307G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483978 | ||||||
| chr1:182484122
|
T | C | 2 | a0003c0003t0001g0050a0003c0003t0001g0295 | 2 | NA18954.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1432-4163T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484122 | ||||||
| chr1:182484360
|
A | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-3925A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484360 | ||||||
| chr1:182484389
|
G | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1432-3896G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484389 | ||||||
| chr1:182484412
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(50): Show | 55 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1432-3873G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484412 | ||||||
| chr1:182484484
|
C | G | 1 | a0003c0003t0001g0155 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1432-3801C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484484 | ||||||
| chr1:182484498
|
G | A | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-3787G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484498 | ||||||
| chr1:182484530
|
A | G | 5 | a0003c0003t0001g0160a0003c0003t0001g0162a0003c0003t0002g0002others(2): Show | 7 | HG02135.hp1 NA18980.hp1 NA19010.hp2 others(4): Show |
intron_variant | MODIFIER | c.1432-3755A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484530 | ||||||
| chr1:182484550
|
A | G | 1 | a0001c0001t0001g0296 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1432-3735A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484550 | ||||||
| chr1:182484784
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(116): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1432-3501C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484784 | ||||||
| chr1:182484820
|
C | T | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-3465C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484820 | ||||||
| chr1:182485015
|
C | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0320 | 2 | HG00408.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1432-3270C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485015 | ||||||
| chr1:182485116
|
C | G | 18 | a0001c0001t0001g0081a0001c0001t0001g0101a0001c0001t0001g0131others(15): Show | 18 | HG00558.hp1 HG00738.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1432-3169C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485116 | ||||||
| chr1:182485238
|
G | A | 1 | a0001c0004t0001g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1432-3047G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485238 | ||||||
| chr1:182485402
|
A | G | 1 | a0003c0003t0002g0256 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1432-2883A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485402 | ||||||
| chr1:182485517
|
A | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-2768A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485517 | ||||||
| chr1:182485582
|
T | C | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-2703T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485582 | ||||||
| chr1:182485609
|
T | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-2676T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485609 | ||||||
| chr1:182485795
|
T | C | 1 | a0003c0003t0001g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1432-2490T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485795 | ||||||
| chr1:182485817
|
G | GA | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1432-2461dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182485817 | |||||
| chr1:182485937
|
T | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(33): Show | 38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1432-2348T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485937 | ||||||
| chr1:182486036
|
C | T | 1 | a0001c0004t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1432-2249C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486036 | ||||||
| chr1:182486195
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(116): Show | 124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1432-2090C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486195 | ||||||
| chr1:182486285
|
C | G | 2 | a0003c0003t0001g0117a0017c0014t0001g0167 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1432-2000C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486285 | ||||||
| chr1:182486310
|
A | AT | 7 | a0001c0001t0001g0114a0001c0001t0001g0182a0001c0001t0001g0269others(4): Show | 7 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1432-1957dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182486310 | |||||
| chr1:182486310
|
AT | A | 20 | a0001c0001t0001g0017a0001c0001t0001g0102a0001c0001t0001g0113others(17): Show | 20 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1432-1957delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182486310 | |||||
| chr1:182486398
|
T | C | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1432-1887T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486398 | ||||||
| chr1:182486553
|
G | A | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1432-1732G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486553 | ||||||
| chr1:182486758
|
C | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-1527C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486758 | ||||||
| chr1:182486762
|
G | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1432-1523G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486762 | ||||||
| chr1:182486783
|
C | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0274 | 2 | NA18944.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1432-1502C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486783 | ||||||
| chr1:182486785
|
C | T | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1432-1500C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486785 | ||||||
| chr1:182486994
|
C | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1432-1291C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486994 | ||||||
| chr1:182487002
|
G | T | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1432-1283G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487002 | ||||||
| chr1:182487012
|
G | C | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1432-1273G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487012 | ||||||
| chr1:182487288
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(47): Show | 52 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1432-997T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487288 | ||||||
| chr1:182487312
|
T | C | 9 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1432-973T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487312 | ||||||
| chr1:182487485
|
T | C | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1432-800T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487485 | ||||||
| chr1:182487712
|
A | G | 4 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0075others(1): Show | 6 | NA18951.hp1 NA18977.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1432-573A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487712 | ||||||
| chr1:182487717
|
C | T | 28 | a0003c0003t0001g0037a0003c0003t0001g0039a0003c0003t0001g0046others(25): Show | 28 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1432-568C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487717 | ||||||
| chr1:182487742
|
A | G | 1 | a0003c0003t0001g0152 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1432-543A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487742 | ||||||
| chr1:182487807
|
A | G | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-478A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487807 | ||||||
| chr1:182487812
|
T | C | 67 | a0003c0003t0001g0016a0003c0003t0001g0029a0003c0003t0001g0037others(64): Show | 70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-473T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487812 | ||||||
| chr1:182487894
|
G | T | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-391G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487894 | ||||||
| chr1:182488147
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1432-138T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182488147 | ||||||
| chr1:182488466
|
ACCAAAGA others(4): Show |
A | 3 | a0001c0001t0001g0201a0001c0001t0001g0272a0001c0005t0001g0271 | 3 | HG02630.hp1 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1494+121_1494+131d others(13): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488466 | |||||
| chr1:182488486
|
C | G | 1 | a0003c0003t0002g0061 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1494+139C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488486 | ||||||
| chr1:182488582
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1494+235C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488582 | ||||||
| chr1:182488642
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(49): Show | 54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1494+295T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488642 | ||||||
| chr1:182488659
|
G | T | 1 | a0002c0002t0001g0078 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1494+312G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488659 | ||||||
| chr1:182488725
|
C | CA | 36 | a0001c0001t0001g0052a0001c0001t0001g0140a0001c0001t0001g0141others(33): Show | 38 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1495-232dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | |||||
| chr1:182488725
|
C | CAAAAAAA others(9): Show |
2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1495-247_1495-232d others(18): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | |||||
| chr1:182488725
|
CAAAAAAA | C | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1495-238_1495-232d others(9): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | |||||
| chr1:182488725
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0112others(1): Show | 4 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495-241_1495-232d others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | |||||
| chr1:182488725
|
CAAAAAAA others(5): Show |
C | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1495-243_1495-232d others(14): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | |||||
| chr1:182488824
|
G | T | 1 | a0001c0004t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1495-156G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488824 | ||||||
| chr1:182489382
|
C | T | 1 | a0002c0002t0001g0157 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1717+180C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489382 | ||||||
| chr1:182489625
|
C | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717+423C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489625 | ||||||
| chr1:182489641
|
C | T | 9 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(6): Show | 9 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1717+439C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489641 | ||||||
| chr1:182489643
|
C | T | 1 | a0004c0009t0001g0225 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1717+441C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489643 | ||||||
| chr1:182489720
|
C | T | 24 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0040others(21): Show | 24 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1717+518C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489720 | ||||||
| chr1:182489742
|
T | C | 5 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG01069.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717+540T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489742 | ||||||
| chr1:182489828
|
T | A | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1717+626T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489828 | ||||||
| chr1:182490455
|
G | A | 1 | a0001c0004t0001g0082 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1717+1253G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182490455 | ||||||
| chr1:182490484
|
G | A | 1 | a0005c0008t0001g0013 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1717+1282G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182490484 | ||||||
| chr1:182490670
|
G | A | 7 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(4): Show | 7 | HG02145.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1717+1468G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182490670 | ||||||
| chr1:182490915
|
C | CT | 191 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(188): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1717+1731dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182490915 | |||||
| chr1:182490915
|
C | CTT | 111 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0017others(108): Show | 116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1717+1730_1717+173 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182490915 | |||||
| chr1:182491042
|
C | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(33): Show | 38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1717+1840C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491042 | ||||||
| chr1:182491057
|
A | AT | 15 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0131others(12): Show | 15 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1717+1867dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182491057 | |||||
| chr1:182491318
|
C | T | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1718-1704C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491318 | ||||||
| chr1:182491319
|
A | G | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1718-1703A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491319 | ||||||
| chr1:182491411
|
C | T | 1 | a0001c0005t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1718-1611C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491411 | ||||||
| chr1:182491490
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1718-1532C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491490 | ||||||
| chr1:182491685
|
GTGA | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(100): Show | 108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1718-1318_1718-131 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182491685 | |||||
| chr1:182491727
|
C | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1718-1295C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491727 | ||||||
| chr1:182491751
|
A | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(8): Show | 11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1718-1271A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491751 | ||||||
| chr1:182491808
|
A | G | 1 | a0004c0012t0001g0326 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1718-1214A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491808 | ||||||
| chr1:182491831
|
GA | G | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1718-1189delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182491831 | |||||
| chr1:182491852
|
A | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(100): Show | 108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1718-1170A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491852 | ||||||
| chr1:182492215
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1718-807T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492215 | ||||||
| chr1:182492320
|
G | C | 1 | a0003c0003t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1718-702G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492320 | ||||||
| chr1:182492328
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1718-694A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492328 | ||||||
| chr1:182492483
|
A | G | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1718-539A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492483 | ||||||
| chr1:182492531
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(178): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1718-491A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492531 | ||||||
| chr1:182492628
|
C | CT | 143 | a0001c0001t0001g0102a0001c0001t0001g0207a0001c0004t0001g0009others(140): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1718-380dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182492628 | |||||
| chr1:182492704
|
C | G | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1718-318C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492704 | ||||||
| chr1:182492773
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1718-249C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492773 | ||||||
| chr1:182493509
|
A | C | 3 | a0001c0001t0001g0199a0001c0005t0001g0327a0001c0005t0001g0330 | 3 | HG02055.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1825+380A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182493509 | ||||||
| chr1:182494110
|
C | T | 1 | a0002c0002t0001g0085 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1825+981C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494110 | ||||||
| chr1:182494190
|
G | C | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+1061G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494190 | ||||||
| chr1:182494309
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1825+1180C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494309 | ||||||
| chr1:182494373
|
C | T | 1 | a0001c0005t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1825+1244C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494373 | ||||||
| chr1:182494548
|
A | G | 2 | a0003c0003t0001g0151a0003c0003t0001g0237 | 2 | NA18950.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1825+1419A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494548 | ||||||
| chr1:182494580
|
A | T | 1 | a0001c0001t0001g0299 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1825+1451A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494580 | ||||||
| chr1:182494740
|
C | T | 1 | a0003c0024t0001g0104 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1825+1611C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494740 | ||||||
| chr1:182494769
|
T | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(100): Show | 108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1825+1640T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494769 | ||||||
| chr1:182494869
|
A | C | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1825+1740A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494869 | ||||||
| chr1:182494973
|
A | G | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+1844A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494973 | ||||||
| chr1:182495107
|
G | T | 6 | a0003c0003t0002g0005a0003c0003t0002g0018a0003c0003t0002g0215others(3): Show | 7 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+1978G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495107 | ||||||
| chr1:182495394
|
A | G | 1 | a0001c0001t0001g0254 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1825+2265A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495394 | ||||||
| chr1:182495461
|
T | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1825+2332T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495461 | ||||||
| chr1:182495524
|
T | C | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+2395T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495524 | ||||||
| chr1:182495623
|
G | A | 1 | a0005c0008t0001g0013 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1825+2494G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495623 | ||||||
| chr1:182495776
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1825+2647T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495776 | ||||||
| chr1:182496143
|
G | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0278 | 2 | HG01258.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1825+3014G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496143 | ||||||
| chr1:182496329
|
T | C | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+3200T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496329 | ||||||
| chr1:182496517
|
C | T | 1 | a0001c0007t0001g0212 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1825+3388C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496517 | ||||||
| chr1:182496615
|
T | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+3486T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496615 | ||||||
| chr1:182496762
|
A | G | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+3633A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496762 | ||||||
| chr1:182496865
|
C | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(33): Show | 38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1825+3736C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496865 | ||||||
| chr1:182496882
|
C | T | 3 | a0001c0006t0001g0208a0001c0006t0001g0209a0001c0006t0001g0210 | 3 | HG01891.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1825+3753C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496882 | ||||||
| chr1:182496888
|
CCTTT | C | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1825+3764_1825+376 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182496888 | |||||
| chr1:182496904
|
T | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+3775T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496904 | ||||||
| chr1:182497179
|
G | C | 30 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0040others(27): Show | 30 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1825+4050G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497179 | ||||||
| chr1:182497224
|
TAGAA | T | 15 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0197others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1825+4099_1825+410 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497224 | |||||
| chr1:182497228
|
A | T | 211 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(208): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1825+4099A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497228 | ||||||
| chr1:182497228
|
AAGAT | A | 39 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(36): Show | 41 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1825+4121_1825+412 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497228 | |||||
| chr1:182497232
|
T | A | 211 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(208): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1825+4103T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497232 | ||||||
| chr1:182497236
|
T | A | 15 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0197others(12): Show | 15 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1825+4107T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497236 | ||||||
| chr1:182497267
|
ATG | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0207a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02965.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+4151_1825+415 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497267 | |||||
| chr1:182497316
|
GATATATA others(40): Show |
G | 1 | a0003c0003t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1825+4198_1825+424 others(51): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497316 | |||||
| chr1:182497326
|
T | TTA | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+4209_1825+421 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497326 | |||||
| chr1:182497436
|
G | A | 1 | a0001c0004t0001g0009 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1825+4307G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497436 | ||||||
| chr1:182497478
|
A | AG | 5 | a0001c0001t0001g0052a0001c0001t0001g0133a0001c0001t0001g0142others(2): Show | 5 | HG00408.hp1 HG02135.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+4350dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497478 | |||||
| chr1:182497556
|
G | T | 1 | a0003c0003t0002g0132 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1825+4427G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497556 | ||||||
| chr1:182497706
|
C | T | 1 | a0003c0003t0002g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1825+4577C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497706 | ||||||
| chr1:182497706
|
CTT | C | 3 | a0001c0007t0001g0021a0001c0007t0001g0022a0001c0007t0001g0212 | 3 | HG02965.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1825+4580_1825+458 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497706 | |||||
| chr1:182497783
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1825+4654C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497783 | ||||||
| chr1:182497828
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+4699T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497828 | ||||||
| chr1:182498082
|
T | G | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1825+4953T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498082 | ||||||
| chr1:182498265
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1825+5136A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498265 | ||||||
| chr1:182498308
|
T | TGTATATG others(12): Show |
190 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(187): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1825+5180_1825+519 others(23): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182498308 | |||||
| chr1:182498309
|
G | GTATATGC others(12): Show |
2 | a0001c0004t0001g0111a0001c0004t0001g0129 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1825+5182_1825+520 others(23): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182498309 | |||||
| chr1:182498363
|
C | A | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1825+5234C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498363 | ||||||
| chr1:182498566
|
C | T | 1 | a0002c0002t0001g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1825+5437C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498566 | ||||||
| chr1:182498732
|
A | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1825+5603A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498732 | ||||||
| chr1:182498796
|
G | GT | 197 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(194): Show | 200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.1825+5670dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182498796 | |||||
| chr1:182498796
|
G | GTT | 16 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(13): Show | 16 | HG01069.hp1 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1825+5669_1825+567 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182498796 | |||||
| chr1:182498800
|
G | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1825+5671G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498800 | ||||||
| chr1:182498949
|
C | A | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+5820C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498949 | ||||||
| chr1:182499158
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1825+6029G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499158 | ||||||
| chr1:182499204
|
T | G | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+6075T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499204 | ||||||
| chr1:182499250
|
G | T | 1 | a0001c0005t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1825+6121G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499250 | ||||||
| chr1:182499296
|
G | T | 1 | a0003c0003t0002g0061 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1825+6167G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499296 | ||||||
| chr1:182499316
|
G | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+6187G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499316 | ||||||
| chr1:182499570
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+6441T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499570 | ||||||
| chr1:182499634
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1825+6505C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499634 | ||||||
| chr1:182499922
|
C | T | 1 | a0001c0004t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1825+6793C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499922 | ||||||
| chr1:182500153
|
C | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+7024C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500153 | ||||||
| chr1:182500359
|
T | G | 2 | a0002c0002t0001g0084a0002c0002t0001g0235 | 2 | HG01928.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1825+7230T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500359 | ||||||
| chr1:182500531
|
A | AT | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+7408dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182500531 | |||||
| chr1:182500604
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1825+7475G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500604 | ||||||
| chr1:182500801
|
A | T | 1 | a0001c0004t0001g0276 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1825+7672A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500801 | ||||||
| chr1:182500950
|
T | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1825+7821T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500950 | ||||||
| chr1:182501002
|
C | T | 148 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0038others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1825+7873C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501002 | ||||||
| chr1:182501115
|
T | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+7986T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501115 | ||||||
| chr1:182501245
|
G | A | 1 | a0003c0003t0001g0151 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1825+8116G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501245 | ||||||
| chr1:182501245
|
G | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(261): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1825+8116G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501245 | ||||||
| chr1:182501266
|
C | CTCTT | 17 | a0001c0004t0001g0092a0001c0004t0001g0217a0001c0004t0001g0234others(14): Show | 17 | HG00423.hp2 HG02027.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1825+8147_1825+815 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501266 | |||||
| chr1:182501280
|
T | C | 207 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(204): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1825+8151T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501280 | ||||||
| chr1:182501282
|
TTTCTTTT others(6): Show |
T | 11 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0113others(8): Show | 11 | HG01243.hp2 HG01346.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1825+8156_1825+816 others(17): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501282 | |||||
| chr1:182501284
|
TC | T | 195 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(192): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1825+8156delC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501284 | ||||||
| chr1:182501295
|
CTT | C | 13 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(10): Show | 13 | HG01258.hp2 HG01884.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825+8171_1825+817 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501295 | |||||
| chr1:182501300
|
T | C | 182 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1825+8171T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501300 | ||||||
| chr1:182501302
|
C | T | 182 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(179): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1825+8173C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501302 | ||||||
| chr1:182501307
|
C | CT | 9 | a0003c0003t0001g0029a0003c0003t0001g0046a0003c0003t0001g0051others(6): Show | 9 | HG00280.hp1 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1825+8208dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | |||||
| chr1:182501307
|
C | T | 13 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(10): Show | 13 | HG01258.hp2 HG01884.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825+8178C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501307 | ||||||
| chr1:182501307
|
CT | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(79): Show | 87 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1825+8208delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | |||||
| chr1:182501307
|
CTT | C | 46 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 48 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1825+8207_1825+820 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | |||||
| chr1:182501307
|
CTTT | C | 8 | a0001c0001t0001g0113a0001c0001t0001g0181a0001c0001t0001g0309others(5): Show | 8 | HG00673.hp2 HG01243.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+8206_1825+820 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | |||||
| chr1:182501307
|
CTTTT | C | 15 | a0001c0004t0001g0092a0001c0004t0001g0217a0001c0004t0001g0234others(12): Show | 15 | HG00423.hp2 HG02148.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1825+8205_1825+820 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | |||||
| chr1:182501309
|
T | C | 13 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(10): Show | 13 | HG01258.hp2 HG01884.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825+8180T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501309 | ||||||
| chr1:182501312
|
T | C | 118 | a0001c0001t0001g0090a0001c0001t0001g0263a0001c0004t0001g0009others(115): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1825+8183T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501312 | ||||||
| chr1:182501313
|
T | C | 62 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(59): Show | 64 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.1825+8184T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501313 | ||||||
| chr1:182501314
|
T | C | 21 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0166others(18): Show | 21 | HG01258.hp2 HG01884.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.1825+8185T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501314 | ||||||
| chr1:182501315
|
T | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(37): Show | 42 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1825+8186T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501315 | ||||||
| chr1:182501316
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1825+8187T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501316 | ||||||
| chr1:182501321
|
T | C | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1825+8192T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501321 | ||||||
| chr1:182501322
|
T | C | 4 | a0001c0001t0001g0113a0001c0001t0001g0181a0001c0001t0001g0306others(1): Show | 4 | HG01243.hp2 HG01346.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825+8193T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501322 | ||||||
| chr1:182501326
|
T | C | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1825+8197T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501326 | ||||||
| chr1:182501327
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1825+8198T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501327 | ||||||
| chr1:182501359
|
G | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1825+8230G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501359 | ||||||
| chr1:182501475
|
C | A | 1 | a0002c0002t0001g0139 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1825+8346C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501475 | ||||||
| chr1:182501555
|
G | C | 17 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(14): Show | 17 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1825+8426G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501555 | ||||||
| chr1:182501721
|
G | A | 1 | a0001c0004t0001g0187 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1825+8592G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501721 | ||||||
| chr1:182501951
|
C | A | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1825+8822C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501951 | ||||||
| chr1:182502020
|
G | T | 1 | a0001c0004t0001g0270 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1825+8891G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502020 | ||||||
| chr1:182502093
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+8964T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502093 | ||||||
| chr1:182502195
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1825+9066C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502195 | ||||||
| chr1:182502237
|
T | C | 1 | a0003c0003t0001g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1825+9108T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502237 | ||||||
| chr1:182502386
|
G | A | 2 | a0003c0003t0002g0025a0003c0003t0002g0059 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1825+9257G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502386 | ||||||
| chr1:182502438
|
C | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1825+9309C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502438 | ||||||
| chr1:182502563
|
T | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1825+9434T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502563 | ||||||
| chr1:182502610
|
G | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(324): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1825+9481G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502610 | ||||||
| chr1:182502812
|
G | C | 2 | a0003c0003t0001g0117a0017c0014t0001g0167 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1825+9683G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502812 | ||||||
| chr1:182502847
|
T | C | 1 | a0010c0025t0001g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1825+9718T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502847 | ||||||
| chr1:182503140
|
C | G | 1 | a0003c0003t0002g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1825+10011C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503140 | ||||||
| chr1:182503184
|
C | T | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1825+10055C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503184 | ||||||
| chr1:182503491
|
G | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1825+10362G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503491 | ||||||
| chr1:182503521
|
T | C | 16 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(13): Show | 16 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1825+10392T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503521 | ||||||
| chr1:182503769
|
T | A | 1 | a0003c0003t0002g0236 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1825+10640T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503769 | ||||||
| chr1:182503837
|
G | A | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(33): Show | 38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1825+10708G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503837 | ||||||
| chr1:182503860
|
A | G | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1825+10731A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503860 | ||||||
| chr1:182503974
|
C | CT | 91 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(88): Show | 96 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1825+10869dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182503974 | |||||
| chr1:182503974
|
C | CTT | 10 | a0001c0001t0001g0064a0001c0001t0001g0141a0001c0001t0001g0304others(7): Show | 10 | HG02040.hp2 HG02135.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+10868_1825+10 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182503974 | |||||
| chr1:182503974
|
CT | C | 179 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1825+10869delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182503974 | |||||
| chr1:182503975
|
T | TC | 9 | a0001c0001t0001g0103a0001c0001t0001g0140a0001c0001t0001g0184others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1825+10846_1825+10 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503975 | ||||||
| chr1:182503976
|
T | C | 36 | a0001c0001t0001g0081a0001c0001t0001g0102a0001c0001t0001g0113others(33): Show | 36 | HG00438.hp1 HG00558.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1825+10847T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503976 | ||||||
| chr1:182503977
|
T | C | 188 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(185): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1825+10848T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503977 | ||||||
| chr1:182503978
|
T | C | 36 | a0001c0001t0001g0081a0001c0001t0001g0113a0001c0001t0001g0166others(33): Show | 36 | HG00438.hp1 HG00558.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1825+10849T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503978 | ||||||
| chr1:182503979
|
T | C | 179 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1825+10850T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503979 | ||||||
| chr1:182503980
|
T | C | 2 | a0002c0002t0001g0012a0002c0002t0001g0074 | 2 | NA18950.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1825+10851T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503980 | ||||||
| chr1:182504022
|
C | T | 138 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0038others(135): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1825+10893C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504022 | ||||||
| chr1:182504073
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1825+10944C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504073 | ||||||
| chr1:182504127
|
C | T | 1 | a0002c0002t0002g0288 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1825+10998C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504127 | ||||||
| chr1:182504200
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1825+11071C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504200 | ||||||
| chr1:182504472
|
C | CT | 32 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0017others(29): Show | 32 | HG00673.hp2 HG00735.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1825+11370dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | |||||
| chr1:182504472
|
C | CTT | 8 | a0001c0001t0001g0114a0001c0001t0001g0141a0001c0001t0001g0191others(5): Show | 8 | HG02027.hp1 HG02040.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+11369_1825+11 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | |||||
| chr1:182504472
|
CTTTT | C | 18 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(15): Show | 18 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1825+11367_1825+11 others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | |||||
| chr1:182504472
|
CTTTTT | C | 82 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1825+11366_1825+11 others(11): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | |||||
| chr1:182504472
|
CTTTTTT | C | 112 | a0001c0001t0001g0182a0001c0001t0001g0197a0001c0001t0001g0198others(109): Show | 114 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1825+11365_1825+11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | |||||
| chr1:182504472
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+11362_1825+11 others(15): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | |||||
| chr1:182504569
|
G | T | 6 | a0003c0003t0001g0037a0003c0003t0001g0050a0003c0003t0001g0159others(3): Show | 6 | HG00673.hp1 HG02074.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+11440G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504569 | ||||||
| chr1:182504594
|
C | T | 6 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+11465C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504594 | ||||||
| chr1:182504841
|
A | G | 2 | a0001c0001t0001g0266a0001c0001t0001g0278 | 2 | HG01258.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1825+11712A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504841 | ||||||
| chr1:182504894
|
C | T | 138 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0038others(135): Show | 140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1825+11765C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504894 | ||||||
| chr1:182505025
|
C | T | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1825+11896C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505025 | ||||||
| chr1:182505118
|
A | G | 4 | a0002c0002t0001g0135a0002c0002t0001g0136a0002c0002t0001g0137others(1): Show | 4 | NA18978.hp2 NA19011.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825+11989A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505118 | ||||||
| chr1:182505140
|
A | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1825+12011A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505140 | ||||||
| chr1:182505224
|
CT | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(100): Show | 108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1825+12097delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182505224 | |||||
| chr1:182505279
|
A | G | 11 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(8): Show | 11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1825+12150A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505279 | ||||||
| chr1:182505339
|
G | T | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1825+12210G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505339 | ||||||
| chr1:182505382
|
T | TG | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1825+12258dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182505382 | |||||
| chr1:182505417
|
C | T | 36 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1825+12288C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505417 | ||||||
| chr1:182505469
|
A | G | 1 | a0016c0022t0001g0073 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1825+12340A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505469 | ||||||
| chr1:182505527
|
G | A | 9 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0166others(6): Show | 9 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1825+12398G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505527 | ||||||
| chr1:182505546
|
T | A | 1 | a0013c0016t0002g0007 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1825+12417T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505546 | ||||||
| chr1:182505569
|
C | T | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1825+12440C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505569 | ||||||
| chr1:182505591
|
T | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1825+12462T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505591 | ||||||
| chr1:182505832
|
C | T | 329 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(326): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1825+12703C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505832 | ||||||
| chr1:182505930
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1825+12801C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505930 | ||||||
| chr1:182505965
|
T | A | 1 | a0001c0001t0001g0250 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1825+12836T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505965 | ||||||
| chr1:182506285
|
G | T | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1825+13156G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506285 | ||||||
| chr1:182506327
|
G | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(41): Show | 45 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1825+13198G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506327 | ||||||
| chr1:182506459
|
A | T | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1825+13330A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506459 | ||||||
| chr1:182506512
|
GC | G | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1825+13384delC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506512 | ||||||
| chr1:182506538
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+13409A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506538 | ||||||
| chr1:182506550
|
T | A | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1825+13421T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506550 | ||||||
| chr1:182506657
|
A | G | 2 | a0001c0004t0001g0214a0002c0002t0001g0329 | 2 | HG02145.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1825+13528A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506657 | ||||||
| chr1:182506841
|
A | G | 1 | a0006c0013t0001g0223 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1825+13712A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506841 | ||||||
| chr1:182506870
|
A | G | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+13741A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506870 | ||||||
| chr1:182506983
|
C | CT | 7 | a0003c0003t0001g0115a0003c0003t0001g0145a0003c0003t0001g0292others(4): Show | 7 | HG00639.hp1 HG01981.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+13877dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182506983 | |||||
| chr1:182506983
|
C | T | 4 | a0003c0003t0001g0160a0003c0003t0001g0162a0003c0003t0002g0002others(1): Show | 6 | HG02135.hp1 NA18980.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825+13854C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506983 | ||||||
| chr1:182506983
|
CT | C | 39 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(36): Show | 41 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1825+13877delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182506983 | |||||
| chr1:182506983
|
CTTT | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0052others(49): Show | 53 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1825+13875_1825+13 others(9): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182506983 | |||||
| chr1:182506983
|
CTTTT | C | 160 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(157): Show | 162 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1825+13874_1825+13 others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182506983 | |||||
| chr1:182506990
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1825+13861T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506990 | ||||||
| chr1:182506991
|
T | C | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1825+13862T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506991 | ||||||
| chr1:182507028
|
T | C | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1825+13899T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507028 | ||||||
| chr1:182507050
|
C | T | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+13921C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507050 | ||||||
| chr1:182507071
|
A | G | 148 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0038others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1825+13942A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507071 | ||||||
| chr1:182507150
|
T | C | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1825+14021T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507150 | ||||||
| chr1:182507178
|
G | A | 1 | a0003c0003t0002g0018 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1825+14049G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507178 | ||||||
| chr1:182507216
|
C | T | 1 | a0002c0002t0001g0032 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1825+14087C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507216 | ||||||
| chr1:182507285
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1825+14156G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507285 | ||||||
| chr1:182507339
|
A | G | 1 | a0003c0003t0002g0310 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1825+14210A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507339 | ||||||
| chr1:182507397
|
C | T | 6 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+14268C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507397 | ||||||
| chr1:182507539
|
G | C | 1 | a0002c0002t0001g0139 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1825+14410G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507539 | ||||||
| chr1:182507690
|
T | C | 1 | a0002c0002t0001g0069 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1826-14314T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507690 | ||||||
| chr1:182507701
|
AT | A | 7 | a0001c0001t0001g0320a0001c0006t0001g0173a0001c0006t0001g0174others(4): Show | 7 | HG01891.hp1 HG02165.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-14291delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182507701 | |||||
| chr1:182508191
|
T | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-13813T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508191 | ||||||
| chr1:182508201
|
C | T | 1 | a0002c0002t0001g0328 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1826-13803C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508201 | ||||||
| chr1:182508231
|
C | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-13773C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508231 | ||||||
| chr1:182508290
|
G | GT | 141 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0043others(138): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1826-13689dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508290 | |||||
| chr1:182508290
|
G | GTT | 78 | a0001c0001t0001g0048a0001c0001t0001g0168a0001c0001t0001g0169others(75): Show | 78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1826-13690_1826-13 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508290 | |||||
| chr1:182508290
|
G | GTTT | 18 | a0001c0001t0001g0103a0001c0001t0001g0166a0001c0001t0001g0184others(15): Show | 18 | HG01175.hp1 HG01928.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1826-13691_1826-13 others(9): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508290 | |||||
| chr1:182508290
|
G | GTTTT | 6 | a0001c0001t0001g0102a0001c0001t0001g0207a0001c0001t0001g0273others(3): Show | 6 | HG02145.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-13692_1826-13 others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508290 | |||||
| chr1:182508293
|
T | C | 1 | a0001c0001t0001g0306 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1826-13711T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508293 | ||||||
| chr1:182508545
|
C | T | 2 | a0002c0002t0001g0328a0002c0002t0001g0329 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1826-13459C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508545 | ||||||
| chr1:182508594
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1826-13410C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508594 | ||||||
| chr1:182508668
|
ATTTGTT | A | 6 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0112others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | |||||
| chr1:182508668
|
ATTTGTTT | A | 74 | a0001c0004t0001g0092a0001c0004t0001g0100a0001c0004t0001g0124others(71): Show | 76 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(13): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | |||||
| chr1:182508668
|
ATTTGTTT others(1): Show |
A | 110 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0052others(107): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(14): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | |||||
| chr1:182508668
|
ATTTGTTT others(2): Show |
A | 18 | a0001c0001t0001g0048a0001c0001t0001g0113a0001c0001t0001g0140others(15): Show | 18 | HG01069.hp1 HG01243.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(15): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | |||||
| chr1:182508668
|
ATTTGTTT others(3): Show |
A | 4 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0007t0001g0212others(1): Show | 4 | HG02559.hp1 HG02895.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(16): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | |||||
| chr1:182508668
|
ATTTGTTT others(4): Show |
A | 3 | a0001c0006t0001g0208a0001c0006t0001g0209a0001c0006t0001g0210 | 3 | HG01891.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(17): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | |||||
| chr1:182508672
|
G | GT | 27 | a0001c0001t0001g0301a0003c0003t0001g0037a0003c0003t0001g0039others(24): Show | 27 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1826-13312dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508672 | |||||
| chr1:182508672
|
GT | G | 15 | a0001c0001t0001g0184a0001c0001t0001g0201a0001c0001t0001g0272others(12): Show | 15 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1826-13312delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508672 | |||||
| chr1:182508692
|
T | A | 18 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(15): Show | 18 | HG00099.hp2 HG00642.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.1826-13312T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508692 | ||||||
| chr1:182508839
|
C | T | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1826-13165C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508839 | ||||||
| chr1:182508904
|
C | T | 3 | a0001c0001t0001g0199a0001c0005t0001g0327a0001c0005t0001g0330 | 3 | HG02055.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1826-13100C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508904 | ||||||
| chr1:182509084
|
T | C | 148 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0038others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1826-12920T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509084 | ||||||
| chr1:182509141
|
C | T | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-12863C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509141 | ||||||
| chr1:182509142
|
G | C | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-12862G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509142 | ||||||
| chr1:182509144
|
C | T | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-12860C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509144 | ||||||
| chr1:182509218
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA18612.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1826-12786G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509218 | ||||||
| chr1:182509228
|
G | A | 2 | a0002c0002t0002g0293a0003c0003t0002g0324 | 2 | HG02027.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1826-12776G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509228 | ||||||
| chr1:182509261
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1826-12743G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509261 | ||||||
| chr1:182509274
|
C | T | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12730C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509274 | ||||||
| chr1:182509284
|
C | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-12720C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509284 | ||||||
| chr1:182509292
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1826-12712C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509292 | ||||||
| chr1:182509306
|
G | A | 1 | a0001c0005t0001g0327 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1826-12698G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509306 | ||||||
| chr1:182509309
|
CAGGGGGC others(167): Show |
C | 1 | a0001c0005t0001g0327 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1826-12694_1826-12 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509309 | ||||||
| chr1:182509310
|
A | G | 214 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1826-12694A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509310 | ||||||
| chr1:182509313
|
GGGCTGAC others(118): Show |
G | 213 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1826-12688_1826-12 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509313 | |||||
| chr1:182509314
|
GGCTGACC others(117): Show |
G | 2 | a0001c0004t0001g0009a0003c0003t0001g0211 | 2 | HG03098.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1826-12688_1826-12 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509314 | |||||
| chr1:182509349
|
TGGCCGGG others(30): Show |
T | 1 | a0003c0003t0002g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1826-12641_1826-12 others(43): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509349 | |||||
| chr1:182509386
|
C | T | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12618C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509386 | ||||||
| chr1:182509415
|
A | G | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-12589A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509415 | ||||||
| chr1:182509418
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-12586C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509418 | ||||||
| chr1:182509424
|
G | A | 6 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1826-12580G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509424 | ||||||
| chr1:182509432
|
GGGCAGAG others(42): Show |
G | 2 | a0003c0003t0001g0117a0017c0014t0001g0167 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1826-12568_1826-12 others(55): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509432 | |||||
| chr1:182509436
|
A | G | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(33): Show | 38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1826-12568A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509436 | ||||||
| chr1:182509438
|
A | G | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12566A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509438 | ||||||
| chr1:182509445
|
AC | A | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-12552delC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509445 | |||||
| chr1:182509467
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1826-12537C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509467 | ||||||
| chr1:182509472
|
C | CGGCTGGC others(71): Show |
2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-12524_1826-12 others(84): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509472 | |||||
| chr1:182509472
|
C | CGGCTGGC others(198): Show |
8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-12524_1826-12 others(211): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509472 | |||||
| chr1:182509481
|
A | G | 46 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(43): Show | 48 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1826-12523A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509481 | ||||||
| chr1:182509484
|
C | G | 1 | a0001c0005t0001g0327 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1826-12520C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509484 | ||||||
| chr1:182509487
|
G | A | 12 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(9): Show | 12 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1826-12517G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509487 | ||||||
| chr1:182509497
|
C | T | 1 | a0003c0003t0002g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1826-12507C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509497 | ||||||
| chr1:182509498
|
C | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-12506C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509498 | ||||||
| chr1:182509522
|
A | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-12482A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509522 | ||||||
| chr1:182509531
|
G | C | 1 | a0001c0001t0001g0305 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1826-12473G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509531 | ||||||
| chr1:182509532
|
GT | G | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12471delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509532 | ||||||
| chr1:182509534
|
G | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12470G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509534 | ||||||
| chr1:182509545
|
C | T | 4 | a0002c0002t0001g0135a0002c0002t0001g0136a0002c0002t0001g0137others(1): Show | 4 | NA18978.hp2 NA19011.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-12459C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509545 | ||||||
| chr1:182509546
|
G | A | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-12458G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509546 | ||||||
| chr1:182509546
|
G | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12458G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509546 | ||||||
| chr1:182509553
|
T | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12451T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509553 | ||||||
| chr1:182509567
|
G | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12437G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509567 | ||||||
| chr1:182509570
|
G | T | 3 | a0001c0007t0001g0021a0001c0007t0001g0022a0001c0007t0001g0212 | 3 | HG02965.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826-12434G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509570 | ||||||
| chr1:182509571
|
T | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12433T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509571 | ||||||
| chr1:182509575
|
T | C | 1 | a0004c0009t0001g0221 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1826-12429T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509575 | ||||||
| chr1:182509580
|
A | G | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12424A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509580 | ||||||
| chr1:182509584
|
T | A | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12420T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509584 | ||||||
| chr1:182509615
|
C | A | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-12389C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509615 | ||||||
| chr1:182509616
|
T | C | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12388T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509616 | ||||||
| chr1:182509641
|
G | A | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12363G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509641 | ||||||
| chr1:182509648
|
GCGGCTGG others(42): Show |
G | 6 | a0003c0003t0001g0047a0003c0003t0001g0062a0003c0003t0001g0089others(3): Show | 6 | HG01981.hp1 HG02273.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-12332_1826-12 others(55): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509648 | |||||
| chr1:182509658
|
G | A | 1 | a0004c0009t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1826-12346G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509658 | ||||||
| chr1:182509671
|
AACCCCCC others(41): Show |
A | 1 | a0003c0003t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1826-12325_1826-12 others(54): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509671 | |||||
| chr1:182509672
|
ACCCCCCA others(42): Show |
A | 1 | a0003c0003t0001g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1826-12311_1826-12 others(55): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509672 | |||||
| chr1:182509697
|
A | G | 1 | a0001c0006t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1826-12307A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509697 | ||||||
| chr1:182509698
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(92): Show | 100 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1826-12306C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509698 | ||||||
| chr1:182509702
|
T | C | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1826-12302T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509702 | ||||||
| chr1:182509706
|
C | T | 13 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(10): Show | 13 | HG01069.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1826-12298C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509706 | ||||||
| chr1:182509718
|
T | A | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12286T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509718 | ||||||
| chr1:182509720
|
A | C | 1 | a0003c0003t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1826-12284A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509720 | ||||||
| chr1:182509738
|
C | A | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12266C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509738 | ||||||
| chr1:182509738
|
C | T | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-12266C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509738 | ||||||
| chr1:182509765
|
G | A | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-12239G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509765 | ||||||
| chr1:182509765
|
G | C | 1 | a0003c0003t0001g0037 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1826-12239G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509765 | ||||||
| chr1:182509796
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1826-12208C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509796 | ||||||
| chr1:182509818
|
A | AC | 21 | a0001c0001t0001g0103a0001c0001t0001g0190a0001c0001t0001g0191others(18): Show | 21 | HG00642.hp1 HG01099.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1826-12177dupC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509818 | |||||
| chr1:182509818
|
AC | A | 16 | a0001c0001t0001g0140a0001c0001t0001g0166a0001c0001t0001g0168others(13): Show | 16 | HG01069.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1826-12177delC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509818 | |||||
| chr1:182509825
|
C | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0030 | 2 | HG02129.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1826-12179C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509825 | ||||||
| chr1:182509825
|
C | T | 4 | a0002c0002t0001g0036a0002c0002t0001g0109a0002c0002t0001g0144others(1): Show | 4 | HG00408.hp2 HG02015.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826-12179C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509825 | ||||||
| chr1:182509827
|
C | A | 1 | a0002c0002t0001g0122 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1826-12177C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509827 | ||||||
| chr1:182509842
|
C | T | 1 | a0003c0003t0001g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1826-12162C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509842 | ||||||
| chr1:182509843
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1826-12161G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509843 | ||||||
| chr1:182509846
|
G | T | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1826-12158G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509846 | ||||||
| chr1:182509848
|
G | A | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-12156G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509848 | ||||||
| chr1:182509854
|
C | T | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1826-12150C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509854 | ||||||
| chr1:182509857
|
G | A | 1 | a0001c0004t0002g0019 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1826-12147G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509857 | ||||||
| chr1:182509967
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1826-12037C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509967 | ||||||
| chr1:182509971
|
C | T | 1 | a0015c0021t0001g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1826-12033C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509971 | ||||||
| chr1:182510007
|
C | T | 148 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0038others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1826-11997C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510007 | ||||||
| chr1:182510047
|
C | T | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-11957C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510047 | ||||||
| chr1:182510096
|
A | G | 33 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(30): Show | 34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-11908A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510096 | ||||||
| chr1:182510097
|
CG | C | 33 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(30): Show | 34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-11906delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510097 | ||||||
| chr1:182510101
|
C | A | 33 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(30): Show | 34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-11903C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510101 | ||||||
| chr1:182510102
|
C | CATGTGA | 33 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(30): Show | 34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-11902_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510102 | ||||||
| chr1:182510111
|
T | C | 1 | a0001c0004t0001g0180 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1826-11893T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510111 | ||||||
| chr1:182510113
|
G | C | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1826-11891G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510113 | ||||||
| chr1:182510137
|
C | T | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1826-11867C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510137 | ||||||
| chr1:182510146
|
T | C | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-11858T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510146 | ||||||
| chr1:182510164
|
G | A | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-11840G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510164 | ||||||
| chr1:182510178
|
G | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-11826G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510178 | ||||||
| chr1:182510215
|
T | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-11789T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510215 | ||||||
| chr1:182510223
|
C | A | 1 | a0001c0004t0001g0009 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1826-11781C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510223 | ||||||
| chr1:182510271
|
C | CG | 15 | a0001c0001t0001g0008a0001c0001t0001g0240a0001c0001t0001g0243others(12): Show | 15 | HG00738.hp1 HG01928.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.1826-11729dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510271 | |||||
| chr1:182510271
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-11733C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510271 | ||||||
| chr1:182510272
|
G | A | 1 | a0003c0003t0002g0179 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1826-11732G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510272 | ||||||
| chr1:182510321
|
G | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(8): Show | 11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826-11683G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510321 | ||||||
| chr1:182510355
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1826-11649C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510355 | ||||||
| chr1:182510409
|
GACTCCGT | G | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-11594_1826-11 others(13): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510409 | ||||||
| chr1:182510417
|
C | G | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-11587C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510417 | ||||||
| chr1:182510420
|
CAATCCCG others(6): Show |
C | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(5): Show | 8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-11583_1826-11 others(19): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510420 | ||||||
| chr1:182510487
|
A | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-11517A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510487 | ||||||
| chr1:182510536
|
C | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-11468C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510536 | ||||||
| chr1:182510537
|
A | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-11467A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510537 | ||||||
| chr1:182510542
|
C | T | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1826-11462C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510542 | ||||||
| chr1:182510543
|
C | T | 2 | a0003c0003t0002g0028a0003c0003t0002g0057 | 2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1826-11461C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510543 | ||||||
| chr1:182510605
|
G | C | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-11399G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510605 | ||||||
| chr1:182510639
|
A | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-11365A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510639 | ||||||
| chr1:182510665
|
T | G | 219 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1826-11339T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510665 | ||||||
| chr1:182510665
|
T | TGAGAGG | 44 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(41): Show | 46 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1826-11302_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510665 | |||||
| chr1:182510665
|
T | TGAGAGGG others(5): Show |
1 | a0001c0001t0001g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1826-11308_1826-11 others(18): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510665 | |||||
| chr1:182510665
|
TGAGAGG | T | 5 | a0003c0003t0001g0062a0003c0003t0001g0115a0003c0003t0001g0149others(2): Show | 5 | HG00544.hp2 HG01981.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-11302_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510665 | |||||
| chr1:182510667
|
A | AGAGGGG | 5 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG01069.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-11332_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510667 | |||||
| chr1:182510667
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0184 | 2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1826-11337A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510667 | ||||||
| chr1:182510669
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1826-11335A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510669 | ||||||
| chr1:182510673
|
A | G | 13 | a0001c0001t0001g0103a0001c0001t0001g0140a0001c0001t0001g0184others(10): Show | 13 | HG01069.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1826-11331A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510673 | ||||||
| chr1:182510675
|
A | AGGGGTAG others(7): Show |
34 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(31): Show | 35 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1826-11326_1826-11 others(20): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510675 | |||||
| chr1:182510675
|
A | AGGGGTAG others(12): Show |
1 | a0001c0001t0001g0263 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1826-11326_1826-11 others(25): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510675 | |||||
| chr1:182510675
|
A | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0005t0001g0271others(2): Show | 5 | HG01884.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-11329A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510675 | ||||||
| chr1:182510679
|
A | AGAGGGG | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-11320_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510679 | |||||
| chr1:182510679
|
A | AGAGGGGG others(5): Show |
6 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(3): Show | 6 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-11320_1826-11 others(18): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510679 | |||||
| chr1:182510679
|
A | AGAGGGGG others(11): Show |
4 | a0001c0001t0001g0113a0001c0001t0001g0181a0002c0002t0001g0313others(1): Show | 4 | HG01243.hp2 HG01346.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-11320_1826-11 others(24): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510679 | |||||
| chr1:182510679
|
A | G | 18 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0140others(15): Show | 18 | HG01069.hp1 HG01884.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.1826-11325A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510679 | ||||||
| chr1:182510681
|
A | G | 39 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(36): Show | 40 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1826-11323A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510681 | ||||||
| chr1:182510685
|
A | G | 191 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0113others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1826-11319A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510685 | ||||||
| chr1:182510687
|
A | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(32): Show | 36 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1826-11317A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510687 | ||||||
| chr1:182510691
|
A | G | 191 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0113others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1826-11313A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510691 | ||||||
| chr1:182510693
|
A | G | 35 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(32): Show | 36 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1826-11311A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510693 | ||||||
| chr1:182510694
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1826-11310G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510694 | ||||||
| chr1:182510694
|
G | GGGGGAGG others(11): Show |
153 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0038others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1826-11308_1826-11 others(24): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510694 | |||||
| chr1:182510694
|
G | GGGGGAGG others(23): Show |
1 | a0005c0008t0001g0042 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1826-11308_1826-11 others(36): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510694 | |||||
| chr1:182510694
|
G | GGGGGAGG others(13): Show |
1 | a0001c0004t0001g0234 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1826-11308_1826-11 others(26): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510694 | |||||
| chr1:182510697
|
A | AAGGG | 34 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(31): Show | 35 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1826-11307_1826-11 others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510697 | ||||||
| chr1:182510697
|
A | AGGGGGAG others(27): Show |
1 | a0001c0001t0001g0247 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1826-11306_1826-11 others(40): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510697 | |||||
| chr1:182510697
|
A | G | 191 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0113others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1826-11307A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510697 | ||||||
| chr1:182510703
|
A | G | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-11301A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510703 | ||||||
| chr1:182510707
|
G | C | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-11297G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510707 | ||||||
| chr1:182510796
|
C | T | 1 | a0001c0004t0001g0040 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1826-11208C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510796 | ||||||
| chr1:182511235
|
G | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-10769G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511235 | ||||||
| chr1:182511283
|
G | A | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1826-10721G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511283 | ||||||
| chr1:182511411
|
G | A | 2 | a0001c0001t0001g0181a0014c0019t0001g0228 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1826-10593G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511411 | ||||||
| chr1:182511422
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1826-10582C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511422 | ||||||
| chr1:182511462
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0112others(1): Show | 4 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-10542G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511462 | ||||||
| chr1:182511568
|
G | T | 16 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(13): Show | 16 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1826-10436G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511568 | ||||||
| chr1:182511650
|
T | A | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1826-10354T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511650 | ||||||
| chr1:182511660
|
A | C | 1 | a0001c0004t0001g0279 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1826-10344A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511660 | ||||||
| chr1:182511734
|
T | C | 192 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1826-10270T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511734 | ||||||
| chr1:182511787
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1826-10217A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511787 | ||||||
| chr1:182511800
|
T | C | 1 | a0003c0003t0002g0110 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1826-10204T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511800 | ||||||
| chr1:182511889
|
G | C | 1 | a0002c0002t0001g0078 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1826-10115G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511889 | ||||||
| chr1:182511945
|
A | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1826-10059A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511945 | ||||||
| chr1:182512008
|
G | A | 1 | a0003c0003t0001g0154 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1826-9996G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512008 | ||||||
| chr1:182512501
|
G | A | 3 | a0003c0003t0001g0159a0003c0003t0001g0258a0003c0003t0001g0259 | 3 | HG00673.hp1 HG02074.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1826-9503G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512501 | ||||||
| chr1:182512553
|
C | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1826-9451C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512553 | ||||||
| chr1:182512579
|
T | C | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-9425T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512579 | ||||||
| chr1:182512783
|
T | C | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1826-9221T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512783 | ||||||
| chr1:182512787
|
G | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-9217G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512787 | ||||||
| chr1:182512815
|
T | C | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-9189T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512815 | ||||||
| chr1:182512916
|
T | C | 1 | a0002c0002t0001g0213 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1826-9088T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512916 | ||||||
| chr1:182513077
|
A | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-8927A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513077 | ||||||
| chr1:182513123
|
G | A | 25 | a0001c0004t0001g0009a0001c0004t0001g0023a0001c0004t0001g0040others(22): Show | 25 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1826-8881G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513123 | ||||||
| chr1:182513147
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1826-8857C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513147 | ||||||
| chr1:182513206
|
G | A | 149 | a0001c0001t0001g0168a0001c0004t0001g0009a0001c0004t0001g0023others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1826-8798G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513206 | ||||||
| chr1:182513239
|
G | A | 3 | a0002c0002t0001g0068a0002c0002t0001g0175a0002c0002t0001g0219 | 3 | HG01074.hp2 HG01192.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1826-8765G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513239 | ||||||
| chr1:182513378
|
A | T | 227 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(224): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1826-8626A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513378 | ||||||
| chr1:182513383
|
T | G | 216 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1826-8621T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513383 | ||||||
| chr1:182513402
|
G | A | 1 | a0002c0002t0001g0213 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1826-8602G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513402 | ||||||
| chr1:182513421
|
C | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1826-8583C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513421 | ||||||
| chr1:182513816
|
G | A | 192 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1826-8188G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513816 | ||||||
| chr1:182513886
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1826-8118T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513886 | ||||||
| chr1:182513897
|
C | CT | 157 | a0001c0001t0001g0190a0001c0001t0001g0197a0001c0001t0001g0198others(154): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1826-8091dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182513897 | |||||
| chr1:182513897
|
CT | C | 19 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0142others(16): Show | 19 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1826-8091delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182513897 | |||||
| chr1:182513981
|
T | C | 1 | a0002c0002t0001g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1826-8023T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513981 | ||||||
| chr1:182514082
|
AG | A | 150 | a0001c0001t0001g0266a0001c0001t0001g0278a0001c0004t0001g0009others(147): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1826-7919delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182514082 | |||||
| chr1:182514164
|
A | T | 192 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1826-7840A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514164 | ||||||
| chr1:182514329
|
G | C | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-7675G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514329 | ||||||
| chr1:182514339
|
A | G | 1 | a0002c0002t0001g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1826-7665A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514339 | ||||||
| chr1:182514375
|
T | C | 1 | a0003c0003t0002g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1826-7629T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514375 | ||||||
| chr1:182514530
|
G | A | 28 | a0003c0003t0001g0037a0003c0003t0001g0039a0003c0003t0001g0046others(25): Show | 28 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1826-7474G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514530 | ||||||
| chr1:182514562
|
G | A | 1 | a0003c0003t0001g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1826-7442G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514562 | ||||||
| chr1:182514567
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(261): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1826-7437T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514567 | ||||||
| chr1:182514673
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1826-7331A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514673 | ||||||
| chr1:182514745
|
G | T | 10 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(7): Show | 10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-7259G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514745 | ||||||
| chr1:182514806
|
G | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(31): Show | 35 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1826-7198G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514806 | ||||||
| chr1:182514854
|
A | T | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(2): Show | 5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-7150A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514854 | ||||||
| chr1:182515037
|
G | A | 6 | a0001c0001t0001g0101a0001c0001t0001g0131a0001c0001t0001g0246others(3): Show | 6 | HG00558.hp1 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1826-6967G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515037 | ||||||
| chr1:182515168
|
G | T | 42 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(39): Show | 43 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1826-6836G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515168 | ||||||
| chr1:182515276
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-6728C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515276 | ||||||
| chr1:182515294
|
C | T | 1 | a0001c0004t0001g0082 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1826-6710C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515294 | ||||||
| chr1:182515348
|
T | C | 10 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(7): Show | 10 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-6656T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515348 | ||||||
| chr1:182515387
|
G | A | 4 | a0002c0002t0001g0135a0002c0002t0001g0136a0002c0002t0001g0137others(1): Show | 4 | NA18978.hp2 NA19011.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-6617G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515387 | ||||||
| chr1:182515400
|
T | C | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1826-6604T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515400 | ||||||
| chr1:182515496
|
A | G | 1 | a0003c0003t0001g0051 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1826-6508A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515496 | ||||||
| chr1:182515552
|
A | AG | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0197others(5): Show | 8 | HG02148.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-6452_1826-645 others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515552 | ||||||
| chr1:182515552
|
A | AGG | 7 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-6452_1826-645 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515552 | ||||||
| chr1:182515552
|
A | AGGG | 3 | a0001c0001t0001g0140a0001c0001t0001g0269a0001c0004t0001g0317 | 3 | HG01175.hp2 HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1826-6452_1826-645 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515552 | ||||||
| chr1:182515552
|
A | G | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-6452A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515552 | ||||||
| chr1:182515553
|
A | AG | 107 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(104): Show | 109 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1826-6443dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182515553 | |||||
| chr1:182515553
|
A | AGG | 48 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0101others(45): Show | 49 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.1826-6444_1826-644 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182515553 | |||||
| chr1:182515553
|
A | G | 28 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0140others(25): Show | 28 | HG01069.hp1 HG01175.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1826-6451A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515553 | ||||||
| chr1:182515570
|
A | G | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-6434A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515570 | ||||||
| chr1:182515574
|
CGT | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(38): Show | 42 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1826-6428_1826-642 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182515574 | |||||
| chr1:182515632
|
C | T | 1 | a0001c0004t0001g0283 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1826-6372C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515632 | ||||||
| chr1:182515932
|
G | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-6072G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515932 | ||||||
| chr1:182516132
|
G | A | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-5872G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516132 | ||||||
| chr1:182516286
|
A | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-5718A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516286 | ||||||
| chr1:182516614
|
T | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-5390T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516614 | ||||||
| chr1:182516664
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-5340G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516664 | ||||||
| chr1:182516709
|
A | AAAC | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-5293_1826-529 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182516709 | |||||
| chr1:182516810
|
T | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-5194T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516810 | ||||||
| chr1:182516913
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1826-5091T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516913 | ||||||
| chr1:182517021
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-4983G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517021 | ||||||
| chr1:182517101
|
G | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-4903G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517101 | ||||||
| chr1:182517201
|
T | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-4803T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517201 | ||||||
| chr1:182517282
|
G | GT | 165 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0140others(162): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1826-4711dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182517282 | |||||
| chr1:182517282
|
G | GTT | 55 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(52): Show | 56 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1826-4712_1826-471 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182517282 | |||||
| chr1:182517285
|
T | TC | 6 | a0001c0004t0002g0019a0001c0004t0002g0044a0001c0004t0002g0054others(3): Show | 6 | NA18941.hp1 NA18965.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-4719_1826-471 others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517285 | ||||||
| chr1:182517376
|
G | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-4628G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517376 | ||||||
| chr1:182517397
|
C | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-4607C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517397 | ||||||
| chr1:182517446
|
T | TG | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-4558_1826-455 others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517446 | ||||||
| chr1:182517591
|
T | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-4413T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517591 | ||||||
| chr1:182517657
|
TTGAGAGC others(9): Show |
T | 1 | a0001c0004t0001g0180 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1826-4346_1826-433 others(20): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517657 | ||||||
| chr1:182517678
|
T | C | 1 | a0001c0004t0001g0180 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1826-4326T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517678 | ||||||
| chr1:182517771
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1826-4233C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517771 | ||||||
| chr1:182517929
|
C | T | 33 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(30): Show | 34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-4075C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517929 | ||||||
| chr1:182517948
|
C | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-4056C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517948 | ||||||
| chr1:182517953
|
G | T | 2 | a0003c0003t0001g0117a0017c0014t0001g0167 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1826-4051G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517953 | ||||||
| chr1:182517993
|
G | A | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-4011G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517993 | ||||||
| chr1:182518007
|
G | GT | 3 | a0001c0004t0001g0231a0001c0004t0001g0257a0001c0004t0001g0287 | 3 | HG01255.hp1 HG01255.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1826-3993dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182518007 | |||||
| chr1:182518071
|
GCT | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-3930_1826-392 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182518071 | |||||
| chr1:182518109
|
G | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-3895G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518109 | ||||||
| chr1:182518187
|
G | A | 1 | a0002c0002t0001g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1826-3817G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518187 | ||||||
| chr1:182518262
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-3742C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518262 | ||||||
| chr1:182518303
|
T | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-3701T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518303 | ||||||
| chr1:182518358
|
T | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-3646T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518358 | ||||||
| chr1:182518420
|
G | C | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-3584G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518420 | ||||||
| chr1:182518509
|
C | A | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826-3495C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518509 | ||||||
| chr1:182518523
|
C | G | 1 | a0001c0001t0001g0240 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1826-3481C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518523 | ||||||
| chr1:182518543
|
C | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-3461C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518543 | ||||||
| chr1:182518767
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-3237C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518767 | ||||||
| chr1:182518816
|
T | C | 11 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(8): Show | 11 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826-3188T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518816 | ||||||
| chr1:182519010
|
T | A | 1 | a0001c0001t0001g0299 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1826-2994T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519010 | ||||||
| chr1:182519010
|
T | TG | 24 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0184others(21): Show | 24 | HG00140.hp2 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1826-2985dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182519010 | |||||
| chr1:182519027
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-2977G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519027 | ||||||
| chr1:182519099
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1826-2905G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519099 | ||||||
| chr1:182519167
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-2837G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519167 | ||||||
| chr1:182519252
|
AT | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-2744delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182519252 | |||||
| chr1:182519494
|
T | TC | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-2507dupC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182519494 | |||||
| chr1:182519515
|
C | T | 11 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(8): Show | 11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826-2489C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519515 | ||||||
| chr1:182519598
|
C | T | 3 | a0001c0005t0001g0171a0009c0011t0001g0185a0009c0011t0001g0186 | 3 | HG01884.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-2406C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519598 | ||||||
| chr1:182519625
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1826-2379G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519625 | ||||||
| chr1:182519743
|
T | G | 1 | a0003c0003t0002g0310 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1826-2261T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519743 | ||||||
| chr1:182519774
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1826-2230C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519774 | ||||||
| chr1:182519843
|
C | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-2161C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519843 | ||||||
| chr1:182519874
|
T | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-2130T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519874 | ||||||
| chr1:182519878
|
A | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-2126A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519878 | ||||||
| chr1:182520002
|
C | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-2002C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520002 | ||||||
| chr1:182520039
|
T | C | 1 | a0001c0004t0001g0082 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1826-1965T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520039 | ||||||
| chr1:182520071
|
T | C | 1 | a0002c0002t0001g0290 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1826-1933T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520071 | ||||||
| chr1:182520080
|
C | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1826-1924C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520080 | ||||||
| chr1:182520133
|
C | T | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-1871C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520133 | ||||||
| chr1:182520343
|
C | G | 5 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(2): Show | 5 | HG01069.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-1661C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520343 | ||||||
| chr1:182520350
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(102): Show | 110 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1826-1654T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520350 | ||||||
| chr1:182520622
|
T | A | 11 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(8): Show | 11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826-1382T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520622 | ||||||
| chr1:182520849
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-1155G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520849 | ||||||
| chr1:182520856
|
G | A | 1 | a0003c0003t0001g0151 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1826-1148G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520856 | ||||||
| chr1:182521054
|
A | G | 3 | a0002c0002t0001g0071a0002c0002t0001g0172a0002c0002t0001g0229 | 3 | HG01109.hp2 HG01169.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1826-950A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521054 | ||||||
| chr1:182521186
|
C | T | 1 | a0002c0002t0001g0138 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1826-818C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521186 | ||||||
| chr1:182521229
|
C | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-775C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521229 | ||||||
| chr1:182521233
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1826-771T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521233 | ||||||
| chr1:182521334
|
A | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-670A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521334 | ||||||
| chr1:182521380
|
A | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-624A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521380 | ||||||
| chr1:182521402
|
A | T | 1 | a0001c0004t0001g0009 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1826-602A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521402 | ||||||
| chr1:182521561
|
T | G | 1 | a0003c0003t0002g0264 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1826-443T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521561 | ||||||
| chr1:182521630
|
A | C | 8 | a0003c0003t0001g0029a0003c0003t0002g0025a0003c0003t0002g0026others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-374A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521630 | ||||||
| chr1:182521733
|
G | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-271G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521733 | ||||||
| chr1:182521825
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-179G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521825 | ||||||
| chr1:182521832
|
A | G | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-172A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521832 | ||||||
| chr1:182521972
|
A | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1826-32A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521972 | ||||||
| chr1:182521976
|
T | C | 31 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(28): Show | 32 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1826-28T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521976 | ||||||
| chr1:182521991
|
AT | A | 8 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(5): Show | 8 | HG00544.hp1 HG01069.hp1 HG02055.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1826-3delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182521991 | |||||
| chr1:182522355
|
T | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1931+246T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522355 | ||||||
| chr1:182522652
|
T | C | 1 | a0002c0002t0001g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1931+543T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522652 | ||||||
| chr1:182522793
|
T | G | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1931+684T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522793 | ||||||
| chr1:182522797
|
T | C | 6 | a0001c0001t0001g0182a0001c0001t0001g0269a0001c0005t0001g0010others(3): Show | 6 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1931+688T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522797 | ||||||
| chr1:182522938
|
T | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+829T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522938 | ||||||
| chr1:182522999
|
G | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+890G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522999 | ||||||
| chr1:182523026
|
C | CT | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+925dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182523026 | |||||
| chr1:182523040
|
A | ATT | 223 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+939_1931+940d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182523040 | |||||
| chr1:182523100
|
A | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+991A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523100 | ||||||
| chr1:182523146
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1931+1037C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523146 | ||||||
| chr1:182523198
|
G | GGC | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+1089_1931+109 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523198 | ||||||
| chr1:182523199
|
T | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+1090T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523199 | ||||||
| chr1:182523200
|
T | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+1091T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523200 | ||||||
| chr1:182523206
|
T | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+1097T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523206 | ||||||
| chr1:182523208
|
C | CT | 38 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(35): Show | 40 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1931+1112dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182523208 | |||||
| chr1:182523208
|
C | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+1099C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523208 | ||||||
| chr1:182523391
|
T | C | 1 | a0003c0003t0002g0026 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1931+1282T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523391 | ||||||
| chr1:182523452
|
A | G | 140 | a0001c0001t0001g0199a0001c0001t0001g0266a0001c0001t0001g0278others(137): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1931+1343A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523452 | ||||||
| chr1:182523509
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+1400G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523509 | ||||||
| chr1:182523545
|
A | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+1436A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523545 | ||||||
| chr1:182523649
|
A | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+1540A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523649 | ||||||
| chr1:182523972
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200 | 3 | HG01069.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1931+1863G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523972 | ||||||
| chr1:182524111
|
A | T | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1931+2002A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524111 | ||||||
| chr1:182524113
|
A | C | 1 | a0003c0003t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1931+2004A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524113 | ||||||
| chr1:182524133
|
C | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+2024C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524133 | ||||||
| chr1:182524167
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1931+2058G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524167 | ||||||
| chr1:182524269
|
T | C | 2 | a0002c0002t0001g0094a0002c0002t0001g0097 | 2 | NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1931+2160T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524269 | ||||||
| chr1:182524291
|
GTA | G | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+2187_1931+218 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182524291 | |||||
| chr1:182524394
|
C | G | 103 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(100): Show | 108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1931+2285C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524394 | ||||||
| chr1:182524630
|
A | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1931+2521A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524630 | ||||||
| chr1:182524650
|
A | T | 15 | a0001c0001t0001g0081a0001c0001t0001g0101a0001c0001t0001g0131others(12): Show | 15 | HG00558.hp1 HG00738.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1931+2541A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524650 | ||||||
| chr1:182524830
|
A | G | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1931+2721A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524830 | ||||||
| chr1:182524928
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-2651G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524928 | ||||||
| chr1:182525010
|
A | G | 1 | a0001c0004t0001g0314 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1932-2569A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525010 | ||||||
| chr1:182525081
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1932-2498C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525081 | ||||||
| chr1:182525102
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-2477G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525102 | ||||||
| chr1:182525104
|
G | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1932-2475G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525104 | ||||||
| chr1:182525380
|
G | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-2199G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525380 | ||||||
| chr1:182525404
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1932-2175T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525404 | ||||||
| chr1:182525463
|
G | A | 1 | a0001c0017t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1932-2116G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525463 | ||||||
| chr1:182525512
|
G | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1932-2067G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525512 | ||||||
| chr1:182525597
|
A | C | 4 | a0001c0005t0001g0271a0001c0007t0001g0021a0001c0007t0001g0022others(1): Show | 4 | HG02647.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-1982A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525597 | ||||||
| chr1:182525860
|
CG | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-1715delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182525860 | |||||
| chr1:182525862
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-1717G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525862 | ||||||
| chr1:182526003
|
A | G | 1 | a0002c0002t0001g0011 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1932-1576A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526003 | ||||||
| chr1:182526057
|
A | G | 1 | a0012c0015t0001g0049 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1932-1522A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526057 | ||||||
| chr1:182526060
|
A | C | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-1519A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526060 | ||||||
| chr1:182526127
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-1452G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526127 | ||||||
| chr1:182526205
|
T | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-1374T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526205 | ||||||
| chr1:182526217
|
C | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-1362C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526217 | ||||||
| chr1:182526337
|
C | T | 7 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(4): Show | 7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1932-1242C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526337 | ||||||
| chr1:182526391
|
G | A | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-1188G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526391 | ||||||
| chr1:182526497
|
G | A | 226 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1932-1082G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526497 | ||||||
| chr1:182526502
|
T | TA | 84 | a0001c0001t0001g0140a0001c0001t0001g0197a0001c0001t0001g0198others(81): Show | 86 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1932-1066dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182526502 | |||||
| chr1:182526578
|
A | G | 215 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(212): Show | 218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1932-1001A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526578 | ||||||
| chr1:182526594
|
C | T | 224 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(221): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1932-985C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526594 | ||||||
| chr1:182526698
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1932-881T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526698 | ||||||
| chr1:182526785
|
GAC | G | 4 | a0001c0001t0001g0191a0001c0001t0001g0301a0001c0001t0001g0303others(1): Show | 4 | NA18977.hp2 NA19000.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1932-790_1932-789d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182526785 | |||||
| chr1:182526789
|
CAT | C | 6 | a0001c0001t0001g0113a0001c0001t0001g0181a0003c0003t0002g0215others(3): Show | 6 | HG01074.hp1 HG01243.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1932-789_1932-788d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526789 | ||||||
| chr1:182526813
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1932-766A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526813 | ||||||
| chr1:182526873
|
T | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1932-706T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526873 | ||||||
| chr1:182527853
|
T | A | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2125+81T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182527853 | ||||||
| chr1:182527886
|
C | A | 149 | a0001c0001t0001g0199a0001c0004t0001g0009a0001c0004t0001g0023others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.2125+114C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182527886 | ||||||
| chr1:182528117
|
G | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2125+345G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528117 | ||||||
| chr1:182528168
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2125+396T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528168 | ||||||
| chr1:182528354
|
T | C | 1 | a0001c0004t0001g0282 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2125+582T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528354 | ||||||
| chr1:182528535
|
G | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125+763G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528535 | ||||||
| chr1:182528716
|
C | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2125+944C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528716 | ||||||
| chr1:182528848
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0253 | 2 | HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2125+1076C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528848 | ||||||
| chr1:182528849
|
G | A | 3 | a0003c0003t0002g0005a0003c0003t0002g0018a0003c0003t0002g0215 | 4 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2125+1077G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528849 | ||||||
| chr1:182528931
|
T | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2125+1159T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528931 | ||||||
| chr1:182529028
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2126-1216C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529028 | ||||||
| chr1:182529289
|
C | T | 2 | a0003c0003t0001g0211a0003c0024t0001g0104 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2126-955C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529289 | ||||||
| chr1:182529492
|
G | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2126-752G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529492 | ||||||
| chr1:182529505
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2126-739A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529505 | ||||||
| chr1:182529524
|
G | A | 1 | a0002c0002t0001g0071 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2126-720G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529524 | ||||||
| chr1:182529759
|
G | A | 2 | a0001c0005t0001g0327a0001c0005t0001g0330 | 2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2126-485G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529759 | ||||||
| chr1:182529776
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-468G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529776 | ||||||
| chr1:182529801
|
T | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-443T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529801 | ||||||
| chr1:182529832
|
G | T | 9 | a0003c0003t0002g0024a0003c0003t0002g0060a0003c0003t0002g0061others(6): Show | 9 | HG00423.hp1 HG01981.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.2126-412G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529832 | ||||||
| chr1:182529884
|
T | A | 2 | a0003c0003t0001g0117a0017c0014t0001g0167 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2126-360T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529884 | ||||||
| chr1:182529910
|
T | C | 2 | a0001c0004t0001g0092a0001c0004t0001g0125 | 2 | NA18969.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2126-334T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529910 | ||||||
| chr1:182529928
|
C | T | 2 | a0001c0004t0001g0040a0001c0004t0001g0321 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2126-316C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529928 | ||||||
| chr1:182529930
|
G | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-314G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529930 | ||||||
| chr1:182529985
|
G | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-259G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529985 | ||||||
| chr1:182530036
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-208A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182530036 | ||||||
| chr1:182530111
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-133G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182530111 | ||||||
| chr1:182530237
|
T | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.2126-7T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182530237 | ||||||
| chr1:182530375
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2243+14A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | chr1 | 182530375 | ||||||
| chr1:182530538
|
T | TAC | 66 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(63): Show | 67 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.2243+203_2243+204d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | |||||
| chr1:182530538
|
T | TACAC | 10 | a0001c0001t0001g0166a0001c0001t0001g0169a0001c0001t0001g0204others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.2243+201_2243+204d others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | |||||
| chr1:182530538
|
T | TACACAC | 5 | a0001c0001t0001g0140a0001c0001t0001g0168a0001c0001t0001g0200others(2): Show | 5 | HG01069.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243+199_2243+204d others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | |||||
| chr1:182530538
|
T | TACACACA others(1): Show |
29 | a0001c0001t0001g0238a0001c0004t0001g0111a0001c0004t0001g0129others(26): Show | 29 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.2243+197_2243+204d others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | |||||
| chr1:182530538
|
T | TACACACA others(3): Show |
102 | a0001c0001t0001g0199a0001c0001t0001g0266a0001c0001t0001g0278others(99): Show | 104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2243+195_2243+204d others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | |||||
| chr1:182530538
|
T | TACACACA others(5): Show |
16 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0004t0001g0100others(13): Show | 16 | HG00544.hp1 HG01109.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.2243+193_2243+204d others(14): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | |||||
| chr1:182530538
|
T | TACACACA others(7): Show |
3 | a0001c0004t0001g0183a0001c0004t0001g0270a0016c0022t0001g0073 | 3 | HG03453.hp2 NA18966.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2243+191_2243+204d others(16): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | |||||
| chr1:182530538
|
TAC | T | 23 | a0001c0001t0001g0056a0001c0001t0001g0093a0001c0001t0001g0102others(20): Show | 24 | HG00423.hp1 HG00544.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2243+203_2243+204d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | |||||
| chr1:182530696
|
G | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2244-94G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | chr1 | 182530696 | ||||||
| chr1:182530993
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2364+83C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182530993 | ||||||
| chr1:182531026
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2364+116A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531026 | ||||||
| chr1:182531412
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2364+502G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531412 | ||||||
| chr1:182531425
|
A | G | 1 | a0001c0004t0001g0252 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2364+515A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531425 | ||||||
| chr1:182531453
|
A | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2364+543A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531453 | ||||||
| chr1:182531681
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2364+771C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531681 | ||||||
| chr1:182531801
|
A | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2365-861A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531801 | ||||||
| chr1:182531831
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2365-831G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531831 | ||||||
| chr1:182531964
|
A | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2365-698A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531964 | ||||||
| chr1:182532021
|
G | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2365-641G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532021 | ||||||
| chr1:182532025
|
C | T | 1 | a0004c0009t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2365-637C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532025 | ||||||
| chr1:182532050
|
C | T | 1 | a0002c0002t0001g0127 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2365-612C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532050 | ||||||
| chr1:182532311
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2365-351A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532311 | ||||||
| chr1:182532311
|
A | T | 2 | a0003c0003t0002g0025a0003c0003t0002g0059 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2365-351A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532311 | ||||||
| chr1:182532373
|
C | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(33): Show | 38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.2365-289C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532373 | ||||||
| chr1:182532374
|
G | A | 150 | a0001c0001t0001g0199a0001c0001t0001g0238a0001c0004t0001g0009others(147): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.2365-288G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532374 | ||||||
| chr1:182532392
|
T | G | 1 | a0003c0003t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2365-270T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532392 | ||||||
| chr1:182532503
|
C | G | 1 | a0002c0002t0001g0098 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2365-159C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532503 | ||||||
| chr1:182532541
|
T | A | 1 | a0001c0001t0001g0302 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2365-121T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532541 | ||||||
| chr1:182532572
|
G | A | 1 | a0004c0009t0001g0220 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2365-90G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532572 | ||||||
| chr1:182532798
|
C | A | 150 | a0001c0001t0001g0199a0001c0001t0001g0238a0001c0004t0001g0009others(147): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
splice_region_variant&intron_variant | LOW | c.2494+7C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182532798 | ||||||
| chr1:182532808
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2494+17T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182532808 | ||||||
| chr1:182532898
|
G | T | 192 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(189): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2494+107G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182532898 | ||||||
| chr1:182533145
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+354G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533145 | ||||||
| chr1:182533189
|
A | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2494+398A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533189 | ||||||
| chr1:182533270
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2494+479C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533270 | ||||||
| chr1:182533296
|
C | CT | 10 | a0001c0001t0001g0182a0001c0001t0001g0216a0001c0001t0001g0269others(7): Show | 10 | HG02015.hp1 HG02109.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2494+522dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533296 | |||||
| chr1:182533296
|
C | CTT | 7 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(4): Show | 7 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2494+521_2494+522d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533296 | |||||
| chr1:182533296
|
C | CTTT | 37 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0017others(34): Show | 39 | HG00438.hp2 HG00544.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2494+520_2494+522d others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533296 | |||||
| chr1:182533296
|
CT | C | 6 | a0001c0001t0001g0233a0001c0001t0001g0265a0001c0004t0001g0276others(3): Show | 6 | HG01884.hp1 HG02602.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494+522delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533296 | |||||
| chr1:182533300
|
T | TTTTTTTT others(99): Show |
2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2494+523_2494+524i others(108): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533300 | |||||
| chr1:182533300
|
T | TTTTTTTT others(98): Show |
27 | a0001c0001t0001g0103a0001c0001t0001g0113a0001c0001t0001g0166others(24): Show | 27 | HG00544.hp2 HG01243.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.2494+512_2494+616d others(107): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533300 | |||||
| chr1:182533300
|
T | TTTTTTTT others(100): Show |
1 | a0003c0003t0001g0295 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2494+522_2494+523i others(109): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533300 | |||||
| chr1:182533300
|
T | TTTTTTTT others(101): Show |
62 | a0001c0001t0001g0250a0003c0003t0001g0016a0003c0003t0001g0029others(59): Show | 65 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.2494+522_2494+523i others(110): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533300 | |||||
| chr1:182533337
|
C | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+546C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533337 | ||||||
| chr1:182533345
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2494+554G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533345 | ||||||
| chr1:182533470
|
G | A | 1 | a0014c0019t0001g0228 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2494+679G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533470 | ||||||
| chr1:182533507
|
T | C | 1 | a0001c0004t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2494+716T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533507 | ||||||
| chr1:182533565
|
A | G | 1 | a0003c0003t0001g0089 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2494+774A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533565 | ||||||
| chr1:182533587
|
G | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2494+796G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533587 | ||||||
| chr1:182533724
|
A | T | 1 | a0002c0002t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2494+933A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533724 | ||||||
| chr1:182533772
|
T | C | 1 | a0001c0004t0001g0282 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2494+981T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533772 | ||||||
| chr1:182533780
|
A | T | 1 | a0002c0002t0001g0099 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2494+989A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533780 | ||||||
| chr1:182533792
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+1001G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533792 | ||||||
| chr1:182533794
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+1003C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533794 | ||||||
| chr1:182533811
|
T | G | 11 | a0001c0001t0001g0113a0001c0001t0001g0166a0001c0001t0001g0168others(8): Show | 11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2494+1020T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533811 | ||||||
| chr1:182533864
|
A | G | 1 | a0002c0002t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2494+1073A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533864 | ||||||
| chr1:182534039
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+1248G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534039 | ||||||
| chr1:182534163
|
A | G | 2 | a0001c0001t0001g0181a0014c0019t0001g0228 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2494+1372A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534163 | ||||||
| chr1:182534570
|
G | A | 1 | a0001c0004t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2494+1779G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534570 | ||||||
| chr1:182534625
|
C | T | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2494+1834C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534625 | ||||||
| chr1:182534734
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+1943A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534734 | ||||||
| chr1:182534742
|
A | T | 40 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(37): Show | 41 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+1951A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534742 | ||||||
| chr1:182534826
|
C | CA | 6 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0247others(3): Show | 6 | HG01978.hp1 HG02738.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.2494+2049dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182534826 | |||||
| chr1:182534848
|
A | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+2057A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534848 | ||||||
| chr1:182535061
|
T | C | 1 | a0002c0002t0001g0099 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2494+2270T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535061 | ||||||
| chr1:182535263
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+2472G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535263 | ||||||
| chr1:182535366
|
AGT | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2494+2586_2494+258 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182535366 | |||||
| chr1:182535508
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+2717G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535508 | ||||||
| chr1:182535527
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+2736A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535527 | ||||||
| chr1:182535764
|
T | C | 2 | a0003c0003t0001g0117a0017c0014t0001g0167 | 2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2494+2973T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535764 | ||||||
| chr1:182535807
|
T | C | 1 | a0002c0002t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2494+3016T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535807 | ||||||
| chr1:182536061
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2494+3270C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536061 | ||||||
| chr1:182536135
|
C | T | 2 | a0003c0003t0001g0151a0003c0003t0001g0237 | 2 | NA18950.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2494+3344C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536135 | ||||||
| chr1:182536208
|
A | G | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2494+3417A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536208 | ||||||
| chr1:182536247
|
C | T | 2 | a0002c0002t0001g0094a0002c0002t0001g0097 | 2 | NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2494+3456C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536247 | ||||||
| chr1:182536279
|
A | G | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+3488A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536279 | ||||||
| chr1:182536498
|
G | A | 2 | a0002c0002t0001g0328a0002c0002t0001g0329 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2494+3707G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536498 | ||||||
| chr1:182536520
|
A | G | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2495-3727A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536520 | ||||||
| chr1:182536542
|
A | G | 141 | a0001c0001t0001g0199a0001c0001t0001g0238a0001c0001t0001g0266others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.2495-3705A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536542 | ||||||
| chr1:182536574
|
C | A | 1 | a0001c0004t0001g0214 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-3673C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536574 | ||||||
| chr1:182536605
|
G | C | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2495-3642G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536605 | ||||||
| chr1:182536620
|
C | T | 8 | a0001c0001t0001g0199a0001c0004t0001g0100a0001c0004t0001g0105others(5): Show | 8 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-3627C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536620 | ||||||
| chr1:182536650
|
C | T | 82 | a0001c0001t0001g0309a0001c0004t0001g0177a0001c0004t0001g0192others(79): Show | 84 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.2495-3597C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536650 | ||||||
| chr1:182536656
|
C | T | 14 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(11): Show | 14 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2495-3591C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536656 | ||||||
| chr1:182536791
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0176a0001c0001t0001g0244others(2): Show | 6 | HG00280.hp2 HG01081.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.2495-3456C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536791 | ||||||
| chr1:182536792
|
G | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0269a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2495-3455G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536792 | ||||||
| chr1:182536849
|
A | G | 1 | a0001c0017t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2495-3398A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536849 | ||||||
| chr1:182536872
|
C | T | 9 | a0001c0001t0001g0102a0001c0001t0001g0140a0001c0001t0001g0182others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-3375C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536872 | ||||||
| chr1:182536940
|
T | C | 1 | a0002c0002t0001g0116 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2495-3307T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536940 | ||||||
| chr1:182536948
|
G | A | 197 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.2495-3299G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536948 | ||||||
| chr1:182537010
|
C | A | 204 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(201): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.2495-3237C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537010 | ||||||
| chr1:182537014
|
T | A | 204 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(201): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.2495-3233T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537014 | ||||||
| chr1:182537036
|
A | G | 12 | a0001c0005t0001g0010a0001c0005t0001g0108a0001c0005t0001g0112others(9): Show | 12 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2495-3211A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537036 | ||||||
| chr1:182537121
|
T | C | 1 | a0002c0002t0001g0165 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2495-3126T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537121 | ||||||
| chr1:182537155
|
T | A | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-3092T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537155 | ||||||
| chr1:182537186
|
C | T | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-3061C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537186 | ||||||
| chr1:182537273
|
C | T | 1 | a0001c0006t0001g0173 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2495-2974C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537273 | ||||||
| chr1:182537303
|
T | G | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2944T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537303 | ||||||
| chr1:182537322
|
T | A | 1 | a0001c0001t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2495-2925T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537322 | ||||||
| chr1:182537342
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2495-2905G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537342 | ||||||
| chr1:182537345
|
T | C | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2902T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537345 | ||||||
| chr1:182537384
|
A | G | 10 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(7): Show | 10 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2495-2863A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537384 | ||||||
| chr1:182537391
|
C | G | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2856C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537391 | ||||||
| chr1:182537450
|
T | C | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2797T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537450 | ||||||
| chr1:182537467
|
A | G | 1 | a0003c0003t0002g0028 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2495-2780A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537467 | ||||||
| chr1:182537492
|
C | T | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2755C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537492 | ||||||
| chr1:182537588
|
C | T | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2659C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537588 | ||||||
| chr1:182537611
|
T | C | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2636T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537611 | ||||||
| chr1:182537687
|
T | C | 10 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(7): Show | 10 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2495-2560T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537687 | ||||||
| chr1:182537739
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-2508G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537739 | ||||||
| chr1:182537774
|
C | A | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2473C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537774 | ||||||
| chr1:182537830
|
T | C | 4 | a0001c0001t0001g0140a0003c0003t0001g0211a0009c0011t0001g0185others(1): Show | 4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2417T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537830 | ||||||
| chr1:182537840
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2495-2407G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537840 | ||||||
| chr1:182537979
|
G | A | 2 | a0001c0001t0001g0140a0003c0003t0001g0211 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2495-2268G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537979 | ||||||
| chr1:182538114
|
C | G | 1 | a0003c0003t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2495-2133C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538114 | ||||||
| chr1:182538229
|
G | C | 1 | a0001c0004t0001g0180 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2495-2018G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538229 | ||||||
| chr1:182538246
|
A | C | 2 | a0006c0013t0001g0223a0006c0013t0001g0224 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2495-2001A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538246 | ||||||
| chr1:182538325
|
C | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-1922C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538325 | ||||||
| chr1:182538336
|
T | C | 124 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0238others(121): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.2495-1911T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538336 | ||||||
| chr1:182538370
|
G | A | 6 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0269others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495-1877G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538370 | ||||||
| chr1:182538436
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0052others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2495-1811G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538436 | ||||||
| chr1:182538459
|
C | T | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2495-1788C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538459 | ||||||
| chr1:182538460
|
G | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2495-1787G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538460 | ||||||
| chr1:182538461
|
G | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2495-1786G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538461 | ||||||
| chr1:182538484
|
T | C | 6 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0269others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495-1763T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538484 | ||||||
| chr1:182538527
|
C | CA | 13 | a0001c0001t0001g0191a0001c0001t0001g0307a0001c0004t0001g0023others(10): Show | 13 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.2495-1706dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182538527 | |||||
| chr1:182538527
|
CA | C | 8 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0269others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-1706delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182538527 | |||||
| chr1:182538667
|
G | GGGA | 7 | a0001c0004t0002g0019a0001c0004t0002g0044a0001c0004t0002g0054others(4): Show | 7 | NA18941.hp1 NA18965.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2495-1577_2495-157 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182538667 | |||||
| chr1:182538670
|
A | G | 5 | a0001c0001t0001g0182a0001c0001t0001g0269a0003c0003t0001g0211others(2): Show | 5 | HG01884.hp1 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-1577A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538670 | ||||||
| chr1:182538746
|
G | A | 1 | a0001c0004t0001g0270 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2495-1501G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538746 | ||||||
| chr1:182538764
|
C | T | 2 | a0001c0001t0001g0140a0003c0003t0001g0211 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2495-1483C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538764 | ||||||
| chr1:182538838
|
C | T | 1 | a0015c0021t0001g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2495-1409C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538838 | ||||||
| chr1:182538864
|
T | A | 1 | a0001c0017t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2495-1383T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538864 | ||||||
| chr1:182538900
|
A | G | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2495-1347A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538900 | ||||||
| chr1:182538909
|
A | G | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2495-1338A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538909 | ||||||
| chr1:182539274
|
CTT | C | 15 | a0001c0001t0001g0238a0001c0004t0001g0009a0001c0004t0001g0023others(12): Show | 15 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.2495-967_2495-966d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182539274 | |||||
| chr1:182539447
|
T | A | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-800T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539447 | ||||||
| chr1:182539448
|
A | G | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-799A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539448 | ||||||
| chr1:182539474
|
A | G | 1 | a0002c0002t0001g0094 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2495-773A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539474 | ||||||
| chr1:182539580
|
A | AC | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-665dupC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182539580 | |||||
| chr1:182539626
|
A | G | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-621A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539626 | ||||||
| chr1:182539656
|
C | T | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-591C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539656 | ||||||
| chr1:182539801
|
A | G | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-446A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539801 | ||||||
| chr1:182539820
|
T | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2495-427T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539820 | ||||||
| chr1:182539913
|
T | C | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-334T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539913 | ||||||
| chr1:182540026
|
G | A | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-221G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182540026 | ||||||
| chr1:182540134
|
G | A | 213 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2495-113G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182540134 | ||||||
| chr1:182540155
|
A | G | 1 | a0001c0017t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2495-92A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182540155 | ||||||
| chr1:182540157
|
A | G | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-90A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182540157 | ||||||
| chr1:182540463
|
T | C | 34 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(31): Show | 36 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.2669+42T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540463 | ||||||
| chr1:182540481
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2669+60C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540481 | ||||||
| chr1:182540482
|
C | A | 122 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0238others(119): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.2669+61C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540482 | ||||||
| chr1:182540482
|
C | G | 6 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0269others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2669+61C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540482 | ||||||
| chr1:182540499
|
A | G | 1 | a0003c0003t0001g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2669+78A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540499 | ||||||
| chr1:182540511
|
T | C | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+90T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540511 | ||||||
| chr1:182540785
|
G | A | 1 | a0001c0004t0001g0100 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2669+364G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540785 | ||||||
| chr1:182540936
|
A | G | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+515A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540936 | ||||||
| chr1:182540978
|
T | G | 1 | a0003c0003t0001g0146 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2669+557T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540978 | ||||||
| chr1:182540999
|
T | C | 7 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2669+578T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540999 | ||||||
| chr1:182541039
|
T | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2669+618T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541039 | ||||||
| chr1:182541053
|
C | T | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+632C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541053 | ||||||
| chr1:182541134
|
G | A | 126 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(123): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.2669+713G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541134 | ||||||
| chr1:182541175
|
C | A | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+754C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541175 | ||||||
| chr1:182541446
|
T | C | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1025T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541446 | ||||||
| chr1:182541527
|
A | G | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2669+1106A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541527 | ||||||
| chr1:182541581
|
G | A | 1 | a0003c0003t0001g0211 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2669+1160G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541581 | ||||||
| chr1:182541765
|
C | T | 2 | a0001c0005t0001g0108a0001c0005t0001g0112 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2669+1344C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541765 | ||||||
| chr1:182541766
|
G | C | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1345G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541766 | ||||||
| chr1:182541840
|
G | A | 1 | a0001c0006t0001g0174 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2669+1419G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541840 | ||||||
| chr1:182542053
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00280.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2669+1632C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542053 | ||||||
| chr1:182542113
|
T | C | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2669+1692T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542113 | ||||||
| chr1:182542114
|
C | T | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1693C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542114 | ||||||
| chr1:182542250
|
G | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2669+1829G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542250 | ||||||
| chr1:182542263
|
T | G | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1842T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542263 | ||||||
| chr1:182542331
|
C | T | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1910C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542331 | ||||||
| chr1:182542346
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2669+1925C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542346 | ||||||
| chr1:182542410
|
T | C | 122 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0238others(119): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.2669+1989T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542410 | ||||||
| chr1:182542537
|
G | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2669+2116G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542537 | ||||||
| chr1:182542577
|
AT | A | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2165delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182542577 | |||||
| chr1:182542599
|
A | G | 2 | a0001c0001t0001g0064a0001c0001t0001g0274 | 2 | NA18944.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2669+2178A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542599 | ||||||
| chr1:182542634
|
A | G | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2213A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542634 | ||||||
| chr1:182542925
|
A | C | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(1): Show | 4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2669+2504A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542925 | ||||||
| chr1:182543000
|
G | T | 2 | a0002c0002t0001g0328a0002c0002t0001g0329 | 2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2669+2579G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543000 | ||||||
| chr1:182543065
|
T | G | 1 | a0001c0004t0001g0009 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2669+2644T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543065 | ||||||
| chr1:182543136
|
A | G | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2715A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543136 | ||||||
| chr1:182543179
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2669+2758C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543179 | ||||||
| chr1:182543192
|
C | A | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2771C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543192 | ||||||
| chr1:182543363
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2669+2942G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543363 | ||||||
| chr1:182543383
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2669+2962A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543383 | ||||||
| chr1:182543411
|
G | A | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2990G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543411 | ||||||
| chr1:182543533
|
A | G | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2669+3112A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543533 | ||||||
| chr1:182543629
|
T | C | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2669+3208T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543629 | ||||||
| chr1:182543708
|
T | G | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2669+3287T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543708 | ||||||
| chr1:182543746
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2669+3325C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543746 | ||||||
| chr1:182543774
|
C | T | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2669+3353C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543774 | ||||||
| chr1:182543775
|
G | A | 6 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0204others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2669+3354G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543775 | ||||||
| chr1:182543851
|
A | G | 2 | a0001c0001t0001g0250a0003c0003t0001g0152 | 2 | NA18963.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2669+3430A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543851 | ||||||
| chr1:182543952
|
A | G | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2669+3531A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543952 | ||||||
| chr1:182544226
|
T | A | 13 | a0001c0005t0001g0010a0001c0005t0001g0108a0001c0005t0001g0112others(10): Show | 13 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2669+3805T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544226 | ||||||
| chr1:182544251
|
T | C | 4 | a0002c0002t0001g0076a0002c0002t0001g0136a0002c0002t0001g0137others(1): Show | 4 | NA18978.hp2 NA19011.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.2669+3830T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544251 | ||||||
| chr1:182544279
|
T | G | 140 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(137): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.2669+3858T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544279 | ||||||
| chr1:182544357
|
C | A | 2 | a0001c0001t0001g0140a0003c0003t0001g0211 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2669+3936C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544357 | ||||||
| chr1:182544558
|
A | G | 128 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2670-3759A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544558 | ||||||
| chr1:182544575
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2670-3742A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544575 | ||||||
| chr1:182544598
|
A | AT | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-3717dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182544598 | |||||
| chr1:182544677
|
T | G | 1 | a0003c0024t0001g0104 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2670-3640T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544677 | ||||||
| chr1:182544735
|
C | T | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-3582C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544735 | ||||||
| chr1:182544801
|
A | G | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-3516A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544801 | ||||||
| chr1:182545058
|
A | G | 124 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0238others(121): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.2670-3259A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545058 | ||||||
| chr1:182545243
|
T | C | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-3074T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545243 | ||||||
| chr1:182545246
|
A | C | 31 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0052others(28): Show | 32 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.2670-3071A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545246 | ||||||
| chr1:182545390
|
T | C | 7 | a0003c0003t0001g0046a0003c0003t0001g0051a0003c0003t0001g0150others(4): Show | 7 | HG00280.hp1 NA18947.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.2670-2927T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545390 | ||||||
| chr1:182545415
|
T | C | 19 | a0001c0001t0001g0238a0001c0001t0001g0266a0001c0001t0001g0278others(16): Show | 19 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.2670-2902T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545415 | ||||||
| chr1:182545494
|
A | C | 1 | a0002c0002t0001g0165 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2670-2823A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545494 | ||||||
| chr1:182545516
|
G | C | 2 | a0001c0001t0001g0140a0003c0003t0001g0211 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2670-2801G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545516 | ||||||
| chr1:182545525
|
T | A | 6 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(3): Show | 6 | HG01069.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2670-2792T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545525 | ||||||
| chr1:182545525
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2670-2792T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545525 | ||||||
| chr1:182545595
|
G | A | 1 | a0001c0004t0001g0128 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2670-2722G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545595 | ||||||
| chr1:182545608
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2670-2709C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545608 | ||||||
| chr1:182545648
|
C | T | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2669C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545648 | ||||||
| chr1:182545711
|
G | T | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2606G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545711 | ||||||
| chr1:182545717
|
T | G | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2600T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545717 | ||||||
| chr1:182545737
|
T | G | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2580T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545737 | ||||||
| chr1:182545908
|
A | G | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2409A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545908 | ||||||
| chr1:182545911
|
T | C | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2406T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545911 | ||||||
| chr1:182545946
|
C | T | 1 | a0012c0015t0001g0049 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2670-2371C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545946 | ||||||
| chr1:182546184
|
GTTTGT | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2670-2128_2670-212 others(9): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182546184 | |||||
| chr1:182546332
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0207 | 2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2670-1985T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546332 | ||||||
| chr1:182546341
|
G | T | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-1976G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546341 | ||||||
| chr1:182546347
|
C | CT | 8 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(5): Show | 8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2670-1958dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182546347 | |||||
| chr1:182546347
|
CT | C | 118 | a0001c0001t0001g0048a0001c0001t0001g0199a0001c0001t0001g0266others(115): Show | 120 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.2670-1958delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182546347 | |||||
| chr1:182546347
|
CTT | C | 9 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0238others(6): Show | 9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2670-1959_2670-195 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182546347 | |||||
| chr1:182546403
|
T | A | 1 | a0003c0003t0002g0005 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2670-1914T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546403 | ||||||
| chr1:182546420
|
C | T | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670-1897C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546420 | ||||||
| chr1:182546550
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2670-1767C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546550 | ||||||
| chr1:182546579
|
G | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2670-1738G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546579 | ||||||
| chr1:182546633
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2670-1684C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546633 | ||||||
| chr1:182546774
|
C | G | 1 | a0001c0004t0001g0286 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2670-1543C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546774 | ||||||
| chr1:182546899
|
G | A | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-1418G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546899 | ||||||
| chr1:182547005
|
T | G | 1 | a0001c0017t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2670-1312T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547005 | ||||||
| chr1:182547097
|
G | T | 1 | a0001c0004t0001g0286 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2670-1220G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547097 | ||||||
| chr1:182547117
|
C | T | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-1200C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547117 | ||||||
| chr1:182547163
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2670-1154A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547163 | ||||||
| chr1:182547244
|
T | C | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-1073T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547244 | ||||||
| chr1:182547383
|
T | TA | 213 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0048others(210): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2670-934_2670-933i others(3): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547383 | ||||||
| chr1:182547419
|
T | C | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-898T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547419 | ||||||
| chr1:182547425
|
T | C | 1 | a0005c0008t0001g0080 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2670-892T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547425 | ||||||
| chr1:182547536
|
T | C | 5 | a0003c0003t0001g0160a0003c0003t0001g0162a0003c0003t0002g0002others(2): Show | 7 | HG02135.hp1 NA18980.hp1 NA19010.hp2 others(4): Show |
intron_variant | MODIFIER | c.2670-781T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547536 | ||||||
| chr1:182547605
|
T | C | 1 | a0002c0002t0001g0120 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2670-712T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547605 | ||||||
| chr1:182547689
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2670-628G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547689 | ||||||
| chr1:182547712
|
T | A | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-605T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547712 | ||||||
| chr1:182547758
|
G | A | 1 | a0003c0003t0002g0215 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2670-559G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547758 | ||||||
| chr1:182547768
|
G | A | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2670-549G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547768 | ||||||
| chr1:182547785
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2670-532C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547785 | ||||||
| chr1:182547816
|
A | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(324): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.2670-501A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547816 | ||||||
| chr1:182547856
|
A | G | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-461A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547856 | ||||||
| chr1:182547860
|
C | CA | 7 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(4): Show | 7 | HG01069.hp1 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2670-447dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182547860 | |||||
| chr1:182547860
|
CA | C | 10 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(7): Show | 10 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2670-447delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182547860 | |||||
| chr1:182548010
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2670-307C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182548010 | ||||||
| chr1:182548103
|
C | A | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-214C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182548103 | ||||||
| chr1:182548222
|
G | C | 130 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-95G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182548222 | ||||||
| chr1:182548479
|
C | G | 2 | a0003c0003t0002g0028a0003c0003t0002g0057 | 2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2808+24C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 16/21 | chr1 | 182548479 | ||||||
| chr1:182548507
|
C | A | 66 | a0001c0001t0001g0006a0001c0001t0001g0043a0001c0001t0001g0052others(63): Show | 67 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.2808+52C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 16/21 | chr1 | 182548507 | ||||||
| chr1:182548916
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2933+92G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182548916 | ||||||
| chr1:182549027
|
T | C | 22 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(19): Show | 22 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2933+203T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549027 | ||||||
| chr1:182549028
|
A | G | 2 | a0008c0010t0001g0205a0008c0010t0001g0206 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2933+204A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549028 | ||||||
| chr1:182549044
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2933+220C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549044 | ||||||
| chr1:182549061
|
C | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0181a0014c0019t0001g0228 | 3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2933+237C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549061 | ||||||
| chr1:182549129
|
G | C | 129 | a0001c0001t0001g0048a0001c0001t0001g0140a0001c0001t0001g0182others(126): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2933+305G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549129 | ||||||
| chr1:182549187
|
G | A | 5 | a0001c0005t0001g0010a0001c0005t0001g0108a0001c0005t0001g0112others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933+363G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549187 | ||||||
| chr1:182549204
|
T | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2933+380T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549204 | ||||||
| chr1:182549279
|
C | T | 129 | a0001c0001t0001g0048a0001c0001t0001g0056a0001c0001t0001g0093others(126): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2933+455C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549279 | ||||||
| chr1:182549310
|
C | T | 2 | a0001c0004t0001g0231a0001c0004t0001g0232 | 2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2933+486C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549310 | ||||||
| chr1:182549347
|
T | G | 1 | a0002c0002t0001g0071 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2933+523T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549347 | ||||||
| chr1:182549356
|
T | C | 1 | a0001c0004t0001g0203 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2933+532T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549356 | ||||||
| chr1:182549489
|
G | A | 17 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.2933+665G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549489 | ||||||
| chr1:182549507
|
T | G | 17 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(14): Show | 17 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.2933+683T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549507 | ||||||
| chr1:182549534
|
T | C | 1 | a0003c0003t0002g0024 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2933+710T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549534 | ||||||
| chr1:182549585
|
G | A | 5 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(2): Show | 5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933+761G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549585 | ||||||
| chr1:182549648
|
G | T | 32 | a0001c0001t0001g0250a0002c0002t0001g0086a0002c0002t0001g0088others(29): Show | 32 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2933+824G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549648 | ||||||
| chr1:182549908
|
A | G | 2 | a0001c0001t0001g0181a0014c0019t0001g0228 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2933+1084A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549908 | ||||||
| chr1:182549977
|
G | C | 1 | a0001c0007t0001g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2934-1123G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549977 | ||||||
| chr1:182550000
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0007c0018t0001g0298 | 3 | HG00438.hp2 NA18962.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.2934-1100G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550000 | ||||||
| chr1:182550148
|
G | A | 8 | a0001c0001t0001g0182a0001c0001t0001g0197a0001c0001t0001g0198others(5): Show | 8 | HG01069.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2934-952G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550148 | ||||||
| chr1:182550223
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2934-877A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550223 | ||||||
| chr1:182550227
|
A | G | 2 | a0001c0005t0001g0108a0001c0005t0001g0112 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2934-873A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550227 | ||||||
| chr1:182550281
|
C | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2934-819C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550281 | ||||||
| chr1:182550299
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(1): Show | 4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2934-801C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550299 | ||||||
| chr1:182550300
|
G | A | 2 | a0001c0004t0001g0234a0001c0004t0001g0276 | 2 | NA18962.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2934-800G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550300 | ||||||
| chr1:182550330
|
A | C | 1 | a0002c0002t0001g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2934-770A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550330 | ||||||
| chr1:182550431
|
G | A | 143 | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0166others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.2934-669G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550431 | ||||||
| chr1:182550436
|
A | G | 34 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(31): Show | 36 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2934-664A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550436 | ||||||
| chr1:182550679
|
AAGT | A | 16 | a0001c0004t0001g0038a0001c0004t0001g0092a0001c0004t0001g0107others(13): Show | 16 | HG01109.hp1 HG02027.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2934-420_2934-418d others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550679 | ||||||
| chr1:182550682
|
T | A | 1 | a0002c0002t0001g0175 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2934-418T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550682 | ||||||
| chr1:182550726
|
A | G | 255 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(252): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2934-374A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550726 | ||||||
| chr1:182550824
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(88): Show | 94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2934-276T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550824 | ||||||
| chr1:182550862
|
A | G | 9 | a0001c0001t0001g0102a0001c0001t0001g0166a0001c0001t0001g0168others(6): Show | 9 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2934-238A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550862 | ||||||
| chr1:182550885
|
T | G | 20 | a0001c0001t0001g0102a0001c0001t0001g0166a0001c0001t0001g0168others(17): Show | 20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2934-215T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550885 | ||||||
| chr1:182550894
|
C | T | 1 | a0001c0004t0001g0177 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2934-206C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550894 | ||||||
| chr1:182550897
|
G | A | 7 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2934-203G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550897 | ||||||
| chr1:182550953
|
G | A | 1 | a0003c0003t0002g0058 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2934-147G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550953 | ||||||
| chr1:182551071
|
C | G | 1 | a0003c0003t0002g0264 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2934-29C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182551071 | ||||||
| chr1:182551221
|
C | T | 3 | a0001c0001t0001g0113a0001c0005t0001g0171a0003c0003t0001g0211 | 3 | HG01346.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3043+12C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551221 | ||||||
| chr1:182551224
|
G | A | 1 | a0003c0024t0001g0104 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3043+15G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551224 | ||||||
| chr1:182551227
|
TCA | T | 16 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.3043+21_3043+22del others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 182551227 | |||||
| chr1:182551292
|
C | G | 1 | a0002c0002t0001g0313 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3043+83C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551292 | ||||||
| chr1:182551477
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(77): Show | 82 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3043+268A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551477 | ||||||
| chr1:182551539
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3043+330C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551539 | ||||||
| chr1:182551569
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3043+360G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551569 | ||||||
| chr1:182551592
|
G | A | 1 | a0003c0003t0001g0016 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3043+383G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551592 | ||||||
| chr1:182551737
|
CAT | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(119): Show | 125 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.3043+540_3043+541d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 182551737 | |||||
| chr1:182551931
|
G | C | 1 | a0003c0003t0002g0161 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3043+722G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551931 | ||||||
| chr1:182551990
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3043+781G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551990 | ||||||
| chr1:182552051
|
G | A | 6 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3043+842G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552051 | ||||||
| chr1:182552117
|
A | AT | 33 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(30): Show | 34 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.3043+922dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 182552117 | |||||
| chr1:182552137
|
G | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(31): Show | 35 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.3043+928G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552137 | ||||||
| chr1:182552183
|
G | A | 15 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0001t0001g0166others(12): Show | 15 | HG01069.hp1 HG01346.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.3043+974G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552183 | ||||||
| chr1:182552239
|
G | A | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3043+1030G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552239 | ||||||
| chr1:182552271
|
G | A | 16 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.3043+1062G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552271 | ||||||
| chr1:182552368
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(243): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.3044-1087T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552368 | ||||||
| chr1:182552403
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3044-1052C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552403 | ||||||
| chr1:182552516
|
C | T | 8 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0001t0001g0197others(5): Show | 8 | HG01069.hp1 HG01346.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3044-939C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552516 | ||||||
| chr1:182552523
|
G | A | 1 | a0002c0002t0001g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3044-932G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552523 | ||||||
| chr1:182552710
|
G | A | 2 | a0001c0004t0001g0170a0001c0004t0001g0270 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3044-745G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552710 | ||||||
| chr1:182552732
|
C | T | 6 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3044-723C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552732 | ||||||
| chr1:182552739
|
C | T | 16 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.3044-716C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552739 | ||||||
| chr1:182552740
|
T | G | 16 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.3044-715T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552740 | ||||||
| chr1:182552755
|
C | T | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(1): Show | 4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3044-700C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552755 | ||||||
| chr1:182553008
|
A | G | 60 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(57): Show | 61 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.3044-447A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182553008 | ||||||
| chr1:182553068
|
C | CTAATTT | 1 | a0001c0001t0001g0001 | 3 | HG01070.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3044-384_3044-379d others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 182553068 | |||||
| chr1:182553157
|
A | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(121): Show | 127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.3044-298A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182553157 | ||||||
| chr1:182553397
|
T | C | 1 | a0002c0002t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3044-58T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182553397 | ||||||
| chr1:182553417
|
C | T | 59 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(56): Show | 60 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.3044-38C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182553417 | ||||||
| chr1:182553627
|
C | A | 16 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.3130+86C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182553627 | ||||||
| chr1:182553789
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3130+248C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182553789 | ||||||
| chr1:182553817
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3130+276A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182553817 | ||||||
| chr1:182553850
|
C | T | 20 | a0001c0001t0001g0102a0001c0001t0001g0166a0001c0001t0001g0168others(17): Show | 20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3130+309C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182553850 | ||||||
| chr1:182554087
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3131-540C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554087 | ||||||
| chr1:182554349
|
T | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3131-278T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554349 | ||||||
| chr1:182554368
|
A | G | 60 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(57): Show | 61 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.3131-259A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554368 | ||||||
| chr1:182554369
|
A | G | 60 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(57): Show | 61 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.3131-258A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554369 | ||||||
| chr1:182554397
|
G | A | 16 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.3131-230G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554397 | ||||||
| chr1:182554456
|
A | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(123): Show | 129 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.3131-171A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554456 | ||||||
| chr1:182554533
|
G | A | 1 | a0002c0002t0001g0313 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3131-94G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554533 | ||||||
| chr1:182554871
|
G | A | 1 | a0001c0005t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3197+178G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182554871 | ||||||
| chr1:182554947
|
A | G | 1 | a0001c0005t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3197+254A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182554947 | ||||||
| chr1:182554967
|
C | T | 1 | a0003c0003t0001g0162 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3197+274C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182554967 | ||||||
| chr1:182555002
|
G | T | 1 | a0001c0004t0002g0123 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.3197+309G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555002 | ||||||
| chr1:182555064
|
G | C | 127 | a0001c0001t0001g0048a0001c0001t0001g0063a0001c0001t0001g0064others(124): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3197+371G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555064 | ||||||
| chr1:182555093
|
T | C | 7 | a0001c0001t0001g0166a0001c0001t0001g0168a0001c0001t0001g0169others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3197+400T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555093 | ||||||
| chr1:182555138
|
C | T | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3197+445C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555138 | ||||||
| chr1:182555143
|
G | A | 8 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0001t0001g0197others(5): Show | 8 | HG01069.hp1 HG01346.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3197+450G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555143 | ||||||
| chr1:182555177
|
C | T | 20 | a0001c0001t0001g0102a0001c0001t0001g0166a0001c0001t0001g0168others(17): Show | 20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3197+484C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555177 | ||||||
| chr1:182555178
|
G | A | 2 | a0001c0004t0001g0285a0003c0003t0001g0149 | 2 | HG00423.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.3197+485G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555178 | ||||||
| chr1:182555214
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3197+521C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555214 | ||||||
| chr1:182555240
|
C | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(121): Show | 127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.3197+547C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555240 | ||||||
| chr1:182555283
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3197+590A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555283 | ||||||
| chr1:182555379
|
A | G | 38 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(35): Show | 39 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.3198-645A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555379 | ||||||
| chr1:182555556
|
T | C | 45 | a0001c0001t0001g0250a0001c0001t0001g0308a0001c0004t0002g0019others(42): Show | 45 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3198-468T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555556 | ||||||
| chr1:182555676
|
G | T | 2 | a0001c0005t0001g0108a0001c0005t0001g0112 | 2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3198-348G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555676 | ||||||
| chr1:182555754
|
C | T | 20 | a0001c0001t0001g0102a0001c0001t0001g0166a0001c0001t0001g0168others(17): Show | 20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3198-270C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555754 | ||||||
| chr1:182556252
|
C | T | 1 | a0001c0005t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.*165+30C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556252 | ||||||
| chr1:182556253
|
G | A | 2 | a0001c0001t0001g0181a0014c0019t0001g0228 | 2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.*165+31G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556253 | ||||||
| chr1:182556395
|
G | A | 1 | a0003c0003t0001g0146 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.*165+173G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556395 | ||||||
| chr1:182556459
|
T | C | 1 | a0003c0003t0001g0155 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.*165+237T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556459 | ||||||
| chr1:182556625
|
C | T | 8 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0001t0001g0197others(5): Show | 8 | HG01069.hp1 HG01346.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.*165+403C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556625 | ||||||
| chr1:182556657
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*165+435T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556657 | ||||||
| chr1:182556669
|
C | A | 6 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.*165+447C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556669 | ||||||
| chr1:182556710
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0269 | 2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*165+488C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556710 | ||||||
| chr1:182556730
|
C | G | 1 | a0011c0023t0001g0134 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.*165+508C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556730 | ||||||
| chr1:182557450
|
G | A | 20 | a0001c0001t0001g0102a0001c0001t0001g0166a0001c0001t0001g0168others(17): Show | 20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.*165+1228G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557450 | ||||||
| chr1:182557530
|
A | T | 1 | a0003c0003t0002g0024 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.*165+1308A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557530 | ||||||
| chr1:182557704
|
C | A | 127 | a0001c0001t0001g0048a0001c0001t0001g0063a0001c0001t0001g0064others(124): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.*165+1482C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557704 | ||||||
| chr1:182557742
|
T | C | 2 | a0001c0005t0001g0327a0001c0005t0001g0330 | 2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*165+1520T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557742 | ||||||
| chr1:182557770
|
A | G | 1 | a0001c0001t0001g0305 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.*165+1548A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557770 | ||||||
| chr1:182557945
|
G | GGAGTGGT others(9): Show |
1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*165+1725_*165+174 others(20): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182557945 | |||||
| chr1:182558003
|
C | T | 1 | a0001c0004t0001g0009 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*165+1781C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558003 | ||||||
| chr1:182558054
|
A | AGAAG | 3 | a0001c0001t0001g0277a0009c0011t0001g0185a0009c0011t0001g0186 | 3 | HG01884.hp1 HG01934.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*165+1855_*165+185 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182558054 | |||||
| chr1:182558054
|
A | AGAAGGAA others(1): Show |
34 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(31): Show | 35 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.*165+1851_*165+185 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182558054 | |||||
| chr1:182558054
|
A | AGAAGGAA others(5): Show |
1 | a0001c0001t0001g0278 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.*165+1847_*165+185 others(16): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182558054 | |||||
| chr1:182558180
|
G | A | 1 | a0003c0003t0002g0236 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.*165+1958G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558180 | ||||||
| chr1:182558225
|
G | A | 2 | a0001c0004t0001g0170a0001c0004t0001g0270 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*165+2003G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558225 | ||||||
| chr1:182558243
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.*165+2021G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558243 | ||||||
| chr1:182558244
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.*165+2022A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558244 | ||||||
| chr1:182558274
|
G | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(33): Show | 37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.*166-2005G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558274 | ||||||
| chr1:182558301
|
G | A | 1 | a0003c0003t0002g0091 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.*166-1978G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558301 | ||||||
| chr1:182558304
|
G | A | 6 | a0001c0001t0001g0103a0001c0001t0001g0184a0001c0001t0001g0201others(3): Show | 6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.*166-1975G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558304 | ||||||
| chr1:182558327
|
AG | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(1): Show | 4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.*166-1949delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182558327 | |||||
| chr1:182558344
|
C | G | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0200others(1): Show | 4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.*166-1935C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558344 | ||||||
| chr1:182558407
|
A | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*166-1872A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558407 | ||||||
| chr1:182558450
|
G | A | 2 | a0002c0002t0001g0094a0002c0002t0001g0097 | 2 | NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.*166-1829G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558450 | ||||||
| chr1:182558641
|
G | A | 4 | a0001c0001t0001g0113a0001c0001t0001g0140a0001c0005t0001g0171others(1): Show | 4 | HG01346.hp2 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.*166-1638G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558641 | ||||||
| chr1:182558670
|
C | A | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*166-1609C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558670 | ||||||
| chr1:182558687
|
A | C | 1 | a0001c0017t0001g0065 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.*166-1592A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558687 | ||||||
| chr1:182558718
|
G | C | 3 | a0002c0002t0001g0109a0002c0002t0001g0144a0002c0002t0001g0260 | 3 | HG02015.hp1 NA18970.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.*166-1561G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558718 | ||||||
| chr1:182558823
|
T | C | 2 | a0009c0011t0001g0185a0009c0011t0001g0186 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*166-1456T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558823 | ||||||
| chr1:182558896
|
C | T | 3 | a0003c0003t0002g0002a0003c0003t0002g0053a0003c0003t0002g0161 | 5 | HG02135.hp1 NA18980.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.*166-1383C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558896 | ||||||
| chr1:182558988
|
T | C | 1 | a0001c0007t0001g0194 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*166-1291T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558988 | ||||||
| chr1:182558994
|
C | T | 11 | a0001c0001t0001g0199a0001c0004t0001g0100a0001c0004t0001g0105others(8): Show | 11 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.*166-1285C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558994 | ||||||
| chr1:182559119
|
C | T | 1 | a0003c0003t0001g0152 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.*166-1160C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559119 | ||||||
| chr1:182559134
|
T | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.*166-1145T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559134 | ||||||
| chr1:182559169
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.*166-1110A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559169 | ||||||
| chr1:182559292
|
T | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(31): Show | 35 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.*166-987T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559292 | ||||||
| chr1:182559298
|
C | T | 34 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(31): Show | 36 | HG00438.hp2 HG00639.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.*166-981C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559298 | ||||||
| chr1:182559358
|
A | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0246 | 2 | HG02040.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.*166-921A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559358 | ||||||
| chr1:182559481
|
G | A | 34 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0081others(31): Show | 35 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.*166-798G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559481 | ||||||
| chr1:182559583
|
C | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-696C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559583 | ||||||
| chr1:182559594
|
C | T | 20 | a0001c0001t0001g0102a0001c0001t0001g0166a0001c0001t0001g0168others(17): Show | 20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.*166-685C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559594 | ||||||
| chr1:182559614
|
T | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-665T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559614 | ||||||
| chr1:182559644
|
C | T | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-635C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559644 | ||||||
| chr1:182559689
|
T | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-590T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559689 | ||||||
| chr1:182559690
|
T | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-589T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559690 | ||||||
| chr1:182559703
|
T | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-576T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559703 | ||||||
| chr1:182559704
|
T | G | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-575T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559704 | ||||||
| chr1:182559708
|
C | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-571C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559708 | ||||||
| chr1:182559711
|
T | G | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-568T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559711 | ||||||
| chr1:182559712
|
T | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-567T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559712 | ||||||
| chr1:182559721
|
C | T | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-558C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559721 | ||||||
| chr1:182559722
|
T | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-557T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559722 | ||||||
| chr1:182559725
|
C | G | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-554C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559725 | ||||||
| chr1:182559729
|
T | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-550T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559729 | ||||||
| chr1:182559750
|
T | C | 5 | a0001c0006t0001g0173a0001c0006t0001g0174a0001c0006t0001g0208others(2): Show | 5 | HG01891.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.*166-529T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559750 | ||||||
| chr1:182559757
|
T | C | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-522T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559757 | ||||||
| chr1:182559758
|
T | C | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-521T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559758 | ||||||
| chr1:182559759
|
G | T | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-520G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559759 | ||||||
| chr1:182559760
|
C | G | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-519C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559760 | ||||||
| chr1:182559764
|
A | C | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-515A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559764 | ||||||
| chr1:182559775
|
C | T | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-504C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559775 | ||||||
| chr1:182559781
|
T | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-498T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559781 | ||||||
| chr1:182559784
|
T | A | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-495T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559784 | ||||||
| chr1:182559794
|
A | T | 1 | a0001c0004t0001g0325 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-485A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559794 | ||||||
| chr1:182559839
|
T | A | 16 | a0001c0004t0001g0177a0001c0004t0001g0180a0001c0004t0001g0192others(13): Show | 16 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.*166-440T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559839 | ||||||
| chr1:182559998
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*166-281A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559998 | ||||||
| chr1:182560189
|
C | G | 1 | a0001c0004t0001g0257 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.*166-90C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182560189 |