Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6721 |
|---|---|
| ensemblid | ENSG00000198911.13 |
| hgncid | 11290 |
| symbol | SREBF2 |
| name | sterol regulatory element binding transcription factor 2 |
| refseq_nuc | NM_004599.4 |
| refseq_prot | NP_004590.2 |
| ensembl_nuc | ENST00000361204.9 |
| ensembl_prot | ENSP00000354476.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 41833105 |
| end | 41907305 |
| strand | + |
| ver | v1.2 |
| region | chr22:41833105-41907305 |
| region5000 | chr22:41828105-41912305 |
| regionname0 | SREBF2_chr22_41833105_41907305 |
| regionname5000 | SREBF2_chr22_41828105_41912305 |
| 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 | 1/0 | 1141 | 158 | 21 | 29 | 78 | 11 | 18 | 60 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002 | 0/0 | 1141 | 136 | 51 | 26 | 42 | 1 | 16 | 34 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0003 | 0/1 | 1141 | 18 | 2 | 4 | 7 | 1 | 3 | 6 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0004 | 0/0 | 1141 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0005 | 0/0 | 1141 | 7 | 0 | 1 | 5 | 1 | 0 | 5 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0006 | 0/0 | 1149 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0007 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0008 | 0/0 | 1141 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0009 | 0/0 | 1141 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0010 | 0/0 | 1141 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3426 | 146 | 17 | 25 | 78 | 9 | 16 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0002 | 0/0 | 3426 | 120 | 39 | 26 | 40 | 1 | 14 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0003 | 0/1 | 3426 | 15 | 0 | 4 | 6 | 1 | 3 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0004 | 0/0 | 3426 | 10 | 10 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0005 | 0/0 | 3426 | 9 | 9 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0006 | 0/0 | 3426 | 6 | 0 | 1 | 4 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0007 | 0/0 | 3426 | 5 | 4 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0008 | 0/0 | 3450 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0009 | 0/0 | 3426 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0010 | 0/0 | 3426 | 2 | 1 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0011 | 0/0 | 3426 | 2 | 0 | 1 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0012 | 0/0 | 3426 | 2 | 0 | 1 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0013 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0014 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0015 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0016 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0017 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0018 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0019 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0020 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0021 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0022 | 0/0 | 3426 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0023 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0024 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0025 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| c0026 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1812 | 175 | 9 | 25 | 109 | 11 | 20 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0002 | 0/0 | 1812 | 54 | 11 | 18 | 9 | 1 | 15 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0003 | 0/0 | 1812 | 37 | 30 | 7 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0004 | 0/1 | 1812 | 24 | 2 | 5 | 11 | 2 | 3 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0005 | 0/0 | 1819 | 8 | 6 | 2 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0006 | 0/0 | 1808 | 6 | 6 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0007 | 0/0 | 1808 | 6 | 6 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0008 | 0/0 | 1812 | 4 | 4 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0009 | 0/0 | 1808 | 4 | 3 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0010 | 0/0 | 1812 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0011 | 0/0 | 1812 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0012 | 0/0 | 1812 | 2 | 0 | 1 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0013 | 0/0 | 1812 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0014 | 0/0 | 1808 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0015 | 0/0 | 1812 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0016 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0017 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0018 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0019 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0020 | 0/0 | 1832 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0021 | 0/0 | 1819 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| t0022 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3426 | 146 | 17 | 25 | 78 | 9 | 16 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0007 | 0/0 | 3426 | 5 | 4 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0011 | 0/0 | 3426 | 2 | 0 | 1 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0012 | 0/0 | 3426 | 2 | 0 | 1 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0020 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0022 | 0/0 | 3426 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0024 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002 | 0/0 | 3426 | 120 | 39 | 26 | 40 | 1 | 14 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0005 | 0/0 | 3426 | 9 | 9 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0009 | 0/0 | 3426 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0013 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0015 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0016 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0018 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0025 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0003c0003 | 0/1 | 3426 | 15 | 0 | 4 | 6 | 1 | 3 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0003c0010 | 0/0 | 3426 | 2 | 1 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0003c0017 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0004c0004 | 0/0 | 3426 | 10 | 10 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0005c0006 | 0/0 | 3426 | 6 | 0 | 1 | 4 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0005c0021 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0006c0008 | 0/0 | 3450 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0007c0026 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0008c0014 | 0/0 | 3426 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0009c0019 | 0/0 | 3426 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0010c0023 | 0/0 | 3426 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5237 | 121 | 4 | 19 | 73 | 9 | 15 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0002 | 0/0 | 5237 | 2 | 0 | 1 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0003 | 0/0 | 5237 | 9 | 7 | 2 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0004 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0005 | 0/0 | 5244 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0008 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0012 | 0/0 | 5237 | 2 | 0 | 1 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0013 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0014 | 0/0 | 5233 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0015 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0017 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0018 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0019 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0001t0020 | 0/0 | 5257 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0007t0003 | 0/0 | 5237 | 5 | 4 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0011t0001 | 0/0 | 5237 | 2 | 0 | 1 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0012t0001 | 0/0 | 5237 | 2 | 0 | 1 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0020t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0022t0001 | 0/0 | 5237 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0001c0024t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002t0001 | 0/0 | 5237 | 37 | 1 | 3 | 31 | 0 | 2 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002t0002 | 0/0 | 5237 | 48 | 9 | 17 | 9 | 1 | 12 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002t0003 | 0/0 | 5237 | 19 | 15 | 4 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002t0005 | 0/0 | 5244 | 7 | 6 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002t0006 | 0/0 | 5233 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002t0008 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002t0009 | 0/0 | 5233 | 4 | 3 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002t0013 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0002t0021 | 0/0 | 5244 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0005t0006 | 0/0 | 5233 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0005t0007 | 0/0 | 5233 | 6 | 6 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0005t0016 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0009t0002 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0013t0001 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0015t0002 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0016t0002 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0018t0004 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0002c0025t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0003c0003t0004 | 0/1 | 5237 | 15 | 0 | 4 | 6 | 1 | 3 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0003c0010t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0003c0010t0022 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0003c0017t0004 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0004c0004t0001 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0004c0004t0003 | 0/0 | 5237 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0004c0004t0006 | 0/0 | 5233 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0004c0004t0010 | 0/0 | 5237 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0004c0004t0011 | 0/0 | 5237 | 2 | 2 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0005c0006t0004 | 0/0 | 5237 | 6 | 0 | 1 | 4 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0005c0021t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0006c0008t0003 | 0/0 | 5261 | 3 | 3 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0007c0026t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0008c0014t0006 | 0/0 | 5233 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0009c0019t0001 | 0/0 | 5237 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| a0010c0023t0001 | 0/0 | 5237 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | copy fasta | chr22 | 41828105 | 41912305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0225 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0008g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0012g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0012g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0013g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0015g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0017g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0018g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0019g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0001t0020g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0007t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0011t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0011t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0012t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0012t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0020t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0022t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0001c0024t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0008g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0009g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0009g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0009g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0002t0021g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0007g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0005t0016g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0009t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0009t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0013t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0015t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0016t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0018t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0002c0025t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0003t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0010t0022g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0003c0017t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0004c0004t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0006t0004g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0005c0021t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0006c0008t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0006c0008t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0006c0008t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0007c0026t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0008c0014t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0009c0019t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| a0010c0023t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0004 | g0134 | EUR | GBR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00099 | hp2 | a0001 | c0020 | t0001 | g0286 | EUR | GBR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | GBR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00280 | hp1 | a0005 | c0006 | t0004 | g0241 | EUR | FIN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0090 | EUR | FIN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | FIN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00639 | hp1 | a0001 | c0001 | t0015 | g0319 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0148 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0026 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00741 | hp1 | a0001 | c0011 | t0001 | g0289 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG00741 | hp2 | a0002 | c0002 | t0003 | g0066 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01081 | hp1 | a0003 | c0003 | t0004 | g0137 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01106 | hp2 | a0002 | c0002 | t0003 | g0024 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01109 | hp2 | a0002 | c0002 | t0009 | g0320 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01169 | hp2 | a0003 | c0003 | t0004 | g0164 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01175 | hp1 | a0002 | c0002 | t0002 | g0110 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0095 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01243 | hp1 | a0002 | c0002 | t0005 | g0021 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01243 | hp2 | a0002 | c0002 | t0003 | g0065 | AMR | PUR | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0098 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01257 | hp2 | a0001 | c0022 | t0001 | g0284 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01358 | hp1 | a0001 | c0012 | t0001 | g0312 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0306 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0317 | EUR | IBS | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01884 | hp1 | a0002 | c0002 | t0006 | g0006 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01891 | hp1 | a0002 | c0002 | t0005 | g0017 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01891 | hp2 | a0002 | c0005 | t0016 | g0251 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0039 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01934 | hp2 | a0001 | c0007 | t0003 | g0007 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01943 | hp2 | a0001 | c0001 | t0012 | g0213 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01981 | hp1 | a0003 | c0003 | t0004 | g0128 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0025 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02027 | hp1 | a0003 | c0003 | t0004 | g0105 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02071 | hp1 | a0007 | c0026 | t0001 | g0308 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02129 | hp2 | a0001 | c0001 | t0017 | g0197 | EAS | KHV | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02145 | hp1 | a0002 | c0013 | t0001 | g0229 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02155 | hp2 | a0001 | c0001 | t0012 | g0178 | EAS | CDX | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02257 | hp1 | a0004 | c0004 | t0011 | g0043 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0067 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02280 | hp1 | a0001 | c0007 | t0003 | g0087 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02280 | hp2 | a0002 | c0002 | t0003 | g0056 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02293 | hp1 | a0005 | c0006 | t0004 | g0297 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0027 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0102 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02300 | hp2 | a0003 | c0003 | t0004 | g0130 | AMR | PEL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02451 | hp1 | a0002 | c0005 | t0007 | g0246 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02572 | hp1 | a0002 | c0002 | t0005 | g0014 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0108 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02615 | hp1 | a0002 | c0009 | t0002 | g0226 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02615 | hp2 | a0006 | c0008 | t0003 | g0115 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02622 | hp1 | a0004 | c0004 | t0011 | g0051 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02622 | hp2 | a0002 | c0002 | t0005 | g0020 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0328 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02630 | hp2 | a0008 | c0014 | t0006 | g0023 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02647 | hp2 | a0002 | c0002 | t0003 | g0058 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0091 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02683 | hp2 | a0001 | c0011 | t0001 | g0262 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0101 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02717 | hp1 | a0002 | c0002 | t0005 | g0015 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02717 | hp2 | a0002 | c0009 | t0002 | g0208 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02723 | hp2 | a0002 | c0002 | t0003 | g0057 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02735 | hp1 | a0002 | c0016 | t0002 | g0083 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02809 | hp1 | a0006 | c0008 | t0003 | g0113 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02809 | hp2 | a0002 | c0005 | t0007 | g0250 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02818 | hp2 | a0004 | c0004 | t0006 | g0049 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0333 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0052 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02896 | hp1 | a0004 | c0004 | t0010 | g0045 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0220 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0053 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02897 | hp2 | a0004 | c0004 | t0010 | g0044 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02965 | hp1 | a0001 | c0007 | t0003 | g0086 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02970 | hp1 | a0002 | c0002 | t0009 | g0322 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0221 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03017 | hp1 | a0003 | c0003 | t0004 | g0125 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0163 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03041 | hp1 | a0002 | c0002 | t0003 | g0055 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0112 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03098 | hp1 | a0002 | c0005 | t0007 | g0252 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03098 | hp2 | a0004 | c0004 | t0001 | g0227 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0080 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03130 | hp2 | a0001 | c0007 | t0003 | g0089 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03139 | hp1 | a0002 | c0002 | t0005 | g0016 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03139 | hp2 | a0002 | c0002 | t0003 | g0008 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03195 | hp1 | a0002 | c0002 | t0021 | g0011 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0244 | AFR | ESN | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0331 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03225 | hp2 | a0003 | c0017 | t0004 | g0041 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03453 | hp1 | a0002 | c0002 | t0009 | g0324 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03453 | hp2 | a0004 | c0004 | t0003 | g0004 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03486 | hp2 | a0001 | c0007 | t0003 | g0088 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0077 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0061 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0059 | AFR | GWD | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03579 | hp1 | a0002 | c0005 | t0006 | g0013 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03669 | hp2 | a0003 | c0003 | t0004 | g0097 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0127 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0037 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0063 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03942 | hp1 | a0003 | c0003 | t0004 | g0158 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03942 | hp2 | a0009 | c0019 | t0001 | g0093 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04115 | hp1 | a0001 | c0024 | t0001 | g0260 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0149 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04199 | hp2 | a0002 | c0015 | t0002 | g0069 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0147 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | STU | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18522 | hp1 | a0002 | c0002 | t0008 | g0332 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18522 | hp2 | a0002 | c0002 | t0009 | g0321 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | CHB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18906 | hp1 | a0003 | c0010 | t0022 | g0022 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18906 | hp2 | a0002 | c0005 | t0007 | g0247 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18939 | hp1 | a0003 | c0003 | t0004 | g0122 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18942 | hp1 | a0005 | c0006 | t0004 | g0124 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18952 | hp1 | a0003 | c0003 | t0004 | g0116 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18959 | hp1 | a0003 | c0003 | t0004 | g0141 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18973 | hp2 | a0003 | c0003 | t0004 | g0123 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18978 | hp2 | a0005 | c0006 | t0004 | g0119 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18979 | hp2 | a0002 | c0025 | t0001 | g0139 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18981 | hp1 | a0010 | c0023 | t0001 | g0203 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18986 | hp2 | a0002 | c0018 | t0004 | g0159 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18987 | hp1 | a0005 | c0021 | t0001 | g0261 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18991 | hp2 | a0003 | c0010 | t0001 | g0145 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19004 | hp1 | a0005 | c0006 | t0004 | g0133 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19010 | hp1 | a0001 | c0001 | t0018 | g0176 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19030 | hp1 | a0004 | c0004 | t0001 | g0042 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0109 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19043 | hp2 | a0002 | c0002 | t0005 | g0019 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19057 | hp2 | a0005 | c0006 | t0004 | g0132 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19068 | hp1 | a0003 | c0003 | t0004 | g0140 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19068 | hp2 | a0001 | c0001 | t0019 | g0195 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19070 | hp1 | a0001 | c0001 | t0020 | g0179 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19240 | hp1 | a0002 | c0002 | t0013 | g0054 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | YRI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0330 | AFR | ASW | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0079 | AFR | ASW | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20752 | hp1 | a0001 | c0012 | t0001 | g0313 | EUR | TSI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | TSI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | TSI | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02109 | hp1 | a0006 | c0008 | t0003 | g0114 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0076 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02486 | hp1 | a0002 | c0005 | t0007 | g0012 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02486 | hp2 | a0002 | c0005 | t0006 | g0249 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02559 | hp1 | a0002 | c0002 | t0006 | g0048 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG02559 | hp2 | a0004 | c0004 | t0010 | g0046 | AFR | ACB | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03471 | hp1 | a0004 | c0004 | t0001 | g0050 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0243 | AFR | MSL | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | USA | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0078 | AFR | USA | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | USA | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | USA | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA21309 | hp1 | a0002 | c0005 | t0007 | g0248 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| NA21309 | hp2 | a0002 | c0002 | t0003 | g0329 | AFR | LWK | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0004 | g0135 | REF | REF | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0225 | REF | REF | SREBF2_chr22_41828105_41912305 | SREBF2 | chr22 | 41828105 | 41912305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41866925
|
T | TAGCAGCA others(17): Show |
1 | a0006 | 3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
conservative_inframe_insertion | MODERATE | c.193_216dupGGCAGCAG others(16): Show |
p.Gly65_Ser72dup | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/19 | 383/5237 | 217/3426 | 73/1141 | INFO_REALIGN_3_PRIME | chr22 | 41866925 | |
| chr22:41867215
|
C | G | 1 | a0007 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.473C>G | p.Thr158Ser | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/19 | 639/5237 | 473/3426 | 158/1141 | chr22 | 41867215 | ||
| chr22:41880738
|
G | C | 5 | a0002a0003a0004others(2): Show | 166 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(163): Show |
missense_variant | MODERATE | c.1784G>C | p.Gly595Ala | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/19 | 1950/5237 | 1784/3426 | 595/1141 | chr22 | 41880738 | ||
| chr22:41880821
|
G | A | 1 | a0004 | 10 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
missense_variant | MODERATE | c.1867G>A | p.Val623Met | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/19 | 2033/5237 | 1867/3426 | 623/1141 | chr22 | 41880821 | ||
| chr22:41884871
|
G | A | 1 | a0010 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.2068G>A | p.Asp690Asn | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/19 | 2234/5237 | 2068/3426 | 690/1141 | chr22 | 41884871 | ||
| chr22:41897118
|
G | A | 1 | a0008 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.2562G>A | p.Met854Ile | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/19 | 2728/5237 | 2562/3426 | 854/1141 | chr22 | 41897118 | ||
| chr22:41897136
|
G | C | 2 | a0003a0005 | 25 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(22): Show |
missense_variant | MODERATE | c.2580G>C | p.Arg860Ser | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/19 | 2746/5237 | 2580/3426 | 860/1141 | chr22 | 41897136 | ||
| chr22:41900377
|
C | T | 1 | a0009 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.2786C>T | p.Ala929Val | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/19 | 2952/5237 | 2786/3426 | 929/1141 | chr22 | 41900377 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41866943
|
T | C | 1 | a0002c0013 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.201T>C | p.Ser67Ser | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/19 | 367/5237 | 201/3426 | 67/1141 | chr22 | 41866943 | ||
| chr22:41867108
|
C | A | 2 | a0002c0005a0008c0014 | 10 | HG01891.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
synonymous_variant | LOW | c.366C>A | p.Pro122Pro | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/19 | 532/5237 | 366/3426 | 122/1141 | chr22 | 41867108 | ||
| chr22:41868771
|
G | A | 1 | a0001c0007 | 5 | HG01934.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.699G>A | p.Ala233Ala | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/19 | 865/5237 | 699/3426 | 233/1141 | chr22 | 41868771 | ||
| chr22:41875637
|
C | T | 1 | a0002c0025 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.1299C>T | p.Pro433Pro | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/19 | 1465/5237 | 1299/3426 | 433/1141 | chr22 | 41875637 | ||
| chr22:41877309
|
C | T | 1 | a0007c0026 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1467C>T | p.Phe489Phe | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/19 | 1633/5237 | 1467/3426 | 489/1141 | chr22 | 41877309 | ||
| chr22:41877330
|
C | T | 1 | a0001c0024 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.1488C>T | p.Pro496Pro | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/19 | 1654/5237 | 1488/3426 | 496/1141 | chr22 | 41877330 | ||
| chr22:41878030
|
G | T | 1 | a0001c0012 | 2 | HG01358.hp1 NA20752.hp1 |
synonymous_variant | LOW | c.1668G>T | p.Leu556Leu | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/19 | 1834/5237 | 1668/3426 | 556/1141 | chr22 | 41878030 | ||
| chr22:41878072
|
C | T | 1 | a0010c0023 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.1710C>T | p.Ser570Ser | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/19 | 1876/5237 | 1710/3426 | 570/1141 | chr22 | 41878072 | ||
| chr22:41878096
|
G | C | 1 | a0002c0015 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1734G>C | p.Arg578Arg | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/19 | 1900/5237 | 1734/3426 | 578/1141 | chr22 | 41878096 | ||
| chr22:41880853
|
G | A | 1 | a0001c0020 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1899G>A | p.Leu633Leu | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/19 | 2065/5237 | 1899/3426 | 633/1141 | chr22 | 41880853 | ||
| chr22:41880898
|
G | A | 1 | a0002c0016 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1944G>A | p.Thr648Thr | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/19 | 2110/5237 | 1944/3426 | 648/1141 | chr22 | 41880898 | ||
| chr22:41884885
|
G | A | 2 | a0001c0011a0001c0024 | 3 | HG00741.hp1 HG02683.hp2 HG04115.hp1 |
synonymous_variant | LOW | c.2082G>A | p.Ala694Ala | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/19 | 2248/5237 | 2082/3426 | 694/1141 | chr22 | 41884885 | ||
| chr22:41894863
|
G | A | 1 | a0002c0009 | 2 | HG02615.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.2421G>A | p.Leu807Leu | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/19 | 2587/5237 | 2421/3426 | 807/1141 | chr22 | 41894863 | ||
| chr22:41904944
|
C | A | 4 | a0002c0018a0003c0003a0003c0017others(1): Show | 23 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(20): Show |
synonymous_variant | LOW | c.3175C>A | p.Arg1059Arg | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/19 | 3341/5237 | 3175/3426 | 1059/1141 | chr22 | 41904944 | ||
| chr22:41905531
|
G | A | 1 | a0001c0022 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.3297G>A | p.Pro1099Pro | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 3463/5237 | 3297/3426 | 1099/1141 | chr22 | 41905531 | ||
| chr22:41905567
|
C | A | 1 | a0003c0017 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.3333C>A | p.Arg1111Arg | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 3499/5237 | 3333/3426 | 1111/1141 | chr22 | 41905567 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41833106
|
T | C | 1 | a0001c0001t0014 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-165T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/19 | 165 | chr22 | 41833106 | |||||
| chr22:41905708
|
T | C | 6 | a0001c0001t0002a0001c0001t0015a0002c0002t0002others(3): Show | 55 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*48T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 48 | chr22 | 41905708 | |||||
| chr22:41905744
|
A | G | 18 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(15): Show | 55 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*84A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 84 | chr22 | 41905744 | |||||
| chr22:41905811
|
C | G | 1 | a0002c0002t0009 | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*151C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 151 | chr22 | 41905811 | |||||
| chr22:41905866
|
G | A | 1 | a0002c0005t0016 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*206G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 206 | chr22 | 41905866 | |||||
| chr22:41905919
|
A | G | 1 | a0003c0010t0022 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*259A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 259 | chr22 | 41905919 | |||||
| chr22:41905939
|
C | T | 6 | a0001c0001t0004a0002c0018t0004a0003c0003t0004others(3): Show | 25 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*279C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 279 | chr22 | 41905939 | |||||
| chr22:41905993
|
C | T | 2 | a0001c0001t0013a0002c0002t0013 | 2 | HG02896.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*333C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 333 | chr22 | 41905993 | |||||
| chr22:41906162
|
G | A | 1 | a0002c0002t0021 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*502G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 502 | chr22 | 41906162 | |||||
| chr22:41906182
|
T | TCTGCGTT others(13): Show |
1 | a0001c0001t0020 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*526_*545dupCGTTCC others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 546 | INFO_REALIGN_3_PRIME | chr22 | 41906182 | ||||
| chr22:41906281
|
T | TGGTGGGA others(4): Show |
3 | a0001c0001t0005a0002c0002t0005a0002c0002t0021 | 9 | HG00639.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*624_*634dupTGGGAG others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 635 | INFO_REALIGN_3_PRIME | chr22 | 41906281 | ||||
| chr22:41906307
|
G | A | 5 | a0001c0001t0002a0002c0002t0002a0002c0009t0002others(2): Show | 54 | HG00280.hp2 HG00642.hp2 HG00733.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*647G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 647 | chr22 | 41906307 | |||||
| chr22:41906322
|
T | C | 1 | a0001c0001t0017 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 662 | chr22 | 41906322 | |||||
| chr22:41906329
|
A | G | 3 | a0001c0001t0008a0002c0002t0008a0002c0005t0007 | 10 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*669A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 669 | chr22 | 41906329 | |||||
| chr22:41906460
|
A | G | 12 | a0001c0001t0005a0001c0001t0008a0001c0001t0014others(9): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*800A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 800 | chr22 | 41906460 | |||||
| chr22:41906520
|
C | T | 1 | a0001c0001t0019 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*860C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 860 | chr22 | 41906520 | |||||
| chr22:41906660
|
G | A | 7 | a0001c0001t0003a0001c0001t0013a0001c0007t0003others(4): Show | 39 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1000G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1000 | chr22 | 41906660 | |||||
| chr22:41906851
|
C | T | 1 | a0001c0001t0018 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1191C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1191 | chr22 | 41906851 | |||||
| chr22:41906906
|
G | A | 12 | a0001c0001t0005a0001c0001t0008a0001c0001t0014others(9): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1246G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1246 | chr22 | 41906906 | |||||
| chr22:41906954
|
G | C | 1 | a0004c0004t0011 | 2 | HG02257.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1294G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1294 | chr22 | 41906954 | |||||
| chr22:41907016
|
G | A | 1 | a0003c0010t0022 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1356G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1356 | chr22 | 41907016 | |||||
| chr22:41907140
|
G | A | 1 | a0001c0001t0012 | 2 | HG01943.hp2 HG02155.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1480G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1480 | chr22 | 41907140 | |||||
| chr22:41907196
|
G | A | 1 | a0004c0004t0010 | 3 | HG02559.hp2 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1536G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1536 | chr22 | 41907196 | |||||
| chr22:41907246
|
TTCAA | T | 10 | a0001c0001t0005a0001c0001t0014a0002c0002t0005others(7): Show | 26 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1594_*1597delATCA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 19/19 | 1594 | INFO_REALIGN_3_PRIME | chr22 | 41907246 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:41833378
|
G | T | 1 | a0002c0002t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.88+20G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833378 | ||||||
| chr22:41833387
|
G | A | 1 | a0004c0004t0003g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.88+29G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833387 | ||||||
| chr22:41833531
|
C | G | 6 | a0002c0002t0003g0328a0002c0002t0003g0329a0002c0002t0003g0330others(3): Show | 6 | HG02630.hp1 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+173C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833531 | ||||||
| chr22:41833558
|
C | T | 75 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(72): Show | 75 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.88+200C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833558 | ||||||
| chr22:41833594
|
G | T | 7 | a0002c0005t0006g0249a0002c0005t0007g0246a0002c0005t0007g0247others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+236G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833594 | ||||||
| chr22:41833625
|
A | G | 1 | a0001c0001t0004g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+267A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833625 | ||||||
| chr22:41833635
|
C | T | 1 | a0001c0001t0002g0327 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.88+277C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41833635 | ||||||
| chr22:41834128
|
C | T | 2 | a0001c0001t0008g0243a0001c0001t0008g0244 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.88+770C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834128 | ||||||
| chr22:41834173
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.88+815G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834173 | ||||||
| chr22:41834345
|
TCA | T | 203 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0253others(200): Show | 204 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.88+990_88+991delCA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41834345 | |||||
| chr22:41834351
|
C | T | 6 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+993C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834351 | ||||||
| chr22:41834468
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.88+1110G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834468 | ||||||
| chr22:41834477
|
T | G | 1 | a0003c0003t0004g0116 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.88+1119T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834477 | ||||||
| chr22:41834584
|
G | A | 1 | a0002c0002t0006g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+1226G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834584 | ||||||
| chr22:41834678
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.88+1320C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834678 | ||||||
| chr22:41834708
|
A | G | 1 | a0002c0002t0002g0111 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.88+1350A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834708 | ||||||
| chr22:41834776
|
T | G | 1 | a0001c0007t0003g0007 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.88+1418T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834776 | ||||||
| chr22:41834931
|
G | C | 1 | a0002c0002t0003g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88+1573G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41834931 | ||||||
| chr22:41835230
|
T | C | 254 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+1872T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835230 | ||||||
| chr22:41835231
|
A | AGCTCACT others(128): Show |
254 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+1875_88+1876ins others(135): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41835231 | |||||
| chr22:41835260
|
C | G | 1 | a0001c0001t0001g0325 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.88+1902C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835260 | ||||||
| chr22:41835309
|
A | AT | 20 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(17): Show | 20 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+1969dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41835309 | |||||
| chr22:41835309
|
AT | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0165a0001c0001t0001g0166others(45): Show | 49 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.88+1969delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41835309 | |||||
| chr22:41835372
|
G | A | 19 | a0001c0001t0003g0010a0001c0001t0005g0018a0002c0002t0005g0014others(16): Show | 19 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+2014G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835372 | ||||||
| chr22:41835387
|
C | G | 1 | a0002c0002t0002g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.88+2029C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835387 | ||||||
| chr22:41835552
|
C | T | 3 | a0002c0002t0001g0106a0002c0002t0001g0107a0003c0003t0004g0105 | 3 | HG00597.hp2 HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.88+2194C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835552 | ||||||
| chr22:41835553
|
G | A | 1 | a0002c0009t0002g0208 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.88+2195G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835553 | ||||||
| chr22:41835597
|
A | C | 4 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207others(1): Show | 4 | HG00673.hp2 NA18971.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+2239A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835597 | ||||||
| chr22:41835602
|
ACCTGGCC others(11): Show |
A | 1 | a0001c0001t0001g0323 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.88+2260_88+2277del others(18): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41835602 | |||||
| chr22:41835875
|
T | C | 2 | a0003c0010t0022g0022a0008c0014t0006g0023 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.88+2517T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835875 | ||||||
| chr22:41835902
|
G | A | 1 | a0002c0002t0003g0008 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88+2544G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41835902 | ||||||
| chr22:41836083
|
T | C | 5 | a0002c0002t0002g0025a0002c0002t0002g0027a0002c0002t0002g0028others(2): Show | 5 | HG00738.hp1 HG01106.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+2725T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836083 | ||||||
| chr22:41836287
|
G | A | 254 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+2929G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836287 | ||||||
| chr22:41836480
|
A | T | 4 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0322others(1): Show | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+3122A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836480 | ||||||
| chr22:41836573
|
C | T | 59 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0007t0003g0007others(56): Show | 60 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.88+3215C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836573 | ||||||
| chr22:41836584
|
G | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0126a0002c0002t0001g0002others(60): Show | 64 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.88+3226G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836584 | ||||||
| chr22:41836784
|
G | C | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.88+3426G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41836784 | ||||||
| chr22:41837035
|
A | G | 2 | a0001c0001t0001g0318a0001c0001t0015g0319 | 2 | HG00639.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.88+3677A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837035 | ||||||
| chr22:41837037
|
G | T | 1 | a0002c0002t0002g0104 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.88+3679G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837037 | ||||||
| chr22:41837046
|
C | T | 18 | a0001c0001t0001g0094a0002c0002t0002g0009a0002c0002t0002g0025others(15): Show | 18 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+3688C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837046 | ||||||
| chr22:41837276
|
G | C | 1 | a0008c0014t0006g0023 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.88+3918G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837276 | ||||||
| chr22:41837367
|
A | G | 1 | a0002c0002t0001g0107 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.88+4009A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837367 | ||||||
| chr22:41837552
|
T | C | 255 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.88+4194T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837552 | ||||||
| chr22:41837556
|
T | TA | 41 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(38): Show | 41 | HG00423.hp1 HG00423.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+4218dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41837556 | |||||
| chr22:41837556
|
TA | T | 17 | a0001c0001t0001g0255a0002c0002t0003g0008a0002c0002t0003g0052others(14): Show | 17 | HG02280.hp2 HG02630.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.88+4218delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41837556 | |||||
| chr22:41837591
|
G | T | 26 | a0001c0001t0003g0010a0001c0001t0004g0245a0001c0001t0005g0018others(23): Show | 26 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.88+4233G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837591 | ||||||
| chr22:41837719
|
G | A | 2 | a0001c0001t0001g0005a0002c0002t0001g0120 | 2 | NA18951.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.88+4361G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837719 | ||||||
| chr22:41837858
|
C | CA | 6 | a0001c0001t0001g0209a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG00733.hp1 HG01258.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+4517dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41837858 | |||||
| chr22:41837858
|
CA | C | 76 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(73): Show | 76 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.88+4517delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41837858 | |||||
| chr22:41837872
|
A | G | 2 | a0002c0002t0002g0090a0002c0002t0002g0091 | 2 | HG00280.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.88+4514A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837872 | ||||||
| chr22:41837935
|
A | G | 3 | a0004c0004t0003g0004a0004c0004t0011g0043a0004c0004t0011g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+4577A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837935 | ||||||
| chr22:41837951
|
G | A | 54 | a0001c0001t0001g0070a0001c0001t0001g0094a0002c0002t0001g0106others(51): Show | 55 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.88+4593G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41837951 | ||||||
| chr22:41838433
|
T | A | 1 | a0001c0001t0003g0010 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.88+5075T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838433 | ||||||
| chr22:41838465
|
GC | G | 6 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316others(3): Show | 6 | HG01106.hp1 HG01358.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+5108delC | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838465 | ||||||
| chr22:41838483
|
A | G | 2 | a0004c0004t0001g0042a0004c0004t0001g0050 | 2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.88+5125A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838483 | ||||||
| chr22:41838607
|
C | T | 1 | a0001c0001t0004g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+5249C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838607 | ||||||
| chr22:41838625
|
T | C | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.88+5267T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838625 | ||||||
| chr22:41838637
|
G | A | 2 | a0002c0002t0003g0328a0002c0002t0003g0333 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.88+5279G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838637 | ||||||
| chr22:41838659
|
G | C | 12 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(9): Show | 12 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+5301G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838659 | ||||||
| chr22:41838933
|
C | T | 190 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0253others(187): Show | 191 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.88+5575C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41838933 | ||||||
| chr22:41839015
|
C | T | 1 | a0008c0014t0006g0023 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.88+5657C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839015 | ||||||
| chr22:41839067
|
G | A | 1 | a0002c0002t0001g0121 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.88+5709G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839067 | ||||||
| chr22:41839143
|
A | T | 3 | a0004c0004t0003g0004a0004c0004t0011g0043a0004c0004t0011g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+5785A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839143 | ||||||
| chr22:41839148
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.88+5790G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839148 | ||||||
| chr22:41839215
|
C | G | 64 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0162others(61): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.88+5857C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839215 | ||||||
| chr22:41839247
|
A | G | 1 | a0002c0002t0001g0002 | 2 | NA18961.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.88+5889A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839247 | ||||||
| chr22:41839300
|
A | G | 1 | a0002c0005t0016g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.88+5942A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839300 | ||||||
| chr22:41839348
|
C | T | 99 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0255others(96): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.88+5990C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839348 | ||||||
| chr22:41839424
|
G | A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.88+6066G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839424 | ||||||
| chr22:41839454
|
G | A | 1 | a0001c0001t0004g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+6096G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839454 | ||||||
| chr22:41839583
|
G | A | 2 | a0003c0010t0022g0022a0008c0014t0006g0023 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.88+6225G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839583 | ||||||
| chr22:41839588
|
C | T | 2 | a0002c0002t0003g0328a0002c0002t0003g0333 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.88+6230C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839588 | ||||||
| chr22:41839651
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.88+6293C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839651 | ||||||
| chr22:41839746
|
C | T | 4 | a0001c0001t0001g0005a0002c0002t0001g0120a0002c0002t0001g0160others(1): Show | 4 | NA18951.hp2 NA18967.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+6388C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839746 | ||||||
| chr22:41839811
|
T | C | 55 | a0001c0001t0001g0070a0001c0001t0001g0094a0002c0002t0001g0106others(52): Show | 56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.88+6453T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839811 | ||||||
| chr22:41839814
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.88+6456A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41839814 | ||||||
| chr22:41839956
|
C | CT | 26 | a0001c0001t0001g0170a0001c0001t0001g0242a0001c0001t0001g0256others(23): Show | 26 | HG00621.hp1 HG00639.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+6619dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41839956 | |||||
| chr22:41839956
|
CT | C | 26 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0008g0112others(23): Show | 26 | HG01884.hp1 HG02109.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+6619delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41839956 | |||||
| chr22:41839956
|
CTT | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0162others(66): Show | 70 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.88+6618_88+6619del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41839956 | |||||
| chr22:41840087
|
T | C | 1 | a0002c0002t0006g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.88+6729T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840087 | ||||||
| chr22:41840100
|
A | G | 2 | a0002c0002t0006g0006a0002c0002t0006g0048 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.88+6742A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840100 | ||||||
| chr22:41840149
|
G | A | 64 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0162others(61): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.88+6791G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840149 | ||||||
| chr22:41840189
|
T | A | 254 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+6831T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840189 | ||||||
| chr22:41840333
|
G | A | 254 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+6975G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840333 | ||||||
| chr22:41840438
|
CTCT | C | 80 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0003g0010others(77): Show | 81 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.88+7085_88+7087del others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41840438 | |||||
| chr22:41840643
|
C | T | 1 | a0001c0001t0003g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.88+7285C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840643 | ||||||
| chr22:41840788
|
A | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0304 | 2 | NA18962.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.88+7430A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41840788 | ||||||
| chr22:41841006
|
C | T | 1 | a0005c0006t0004g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88+7648C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841006 | ||||||
| chr22:41841063
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.88+7705C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841063 | ||||||
| chr22:41841130
|
G | C | 1 | a0001c0001t0003g0210 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.88+7772G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841130 | ||||||
| chr22:41841271
|
T | G | 1 | a0002c0002t0009g0321 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.88+7913T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841271 | ||||||
| chr22:41841396
|
T | G | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.88+8038T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841396 | ||||||
| chr22:41841561
|
C | T | 254 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+8203C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841561 | ||||||
| chr22:41841594
|
G | T | 1 | a0005c0006t0004g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88+8236G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841594 | ||||||
| chr22:41841668
|
ACTC | A | 3 | a0001c0001t0001g0165a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | NA18978.hp1 NA18986.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.88+8314_88+8316del others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41841668 | |||||
| chr22:41841765
|
C | T | 254 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+8407C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41841765 | ||||||
| chr22:41842023
|
A | C | 64 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0162others(61): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.88+8665A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842023 | ||||||
| chr22:41842138
|
A | T | 1 | a0001c0001t0001g0303 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.88+8780A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842138 | ||||||
| chr22:41842236
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.88+8878G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842236 | ||||||
| chr22:41842715
|
C | G | 2 | a0001c0001t0001g0202a0010c0023t0001g0203 | 2 | NA18967.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.88+9357C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842715 | ||||||
| chr22:41842749
|
G | A | 1 | a0001c0007t0003g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.88+9391G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842749 | ||||||
| chr22:41842760
|
C | T | 4 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316others(1): Show | 4 | HG01106.hp1 HG01517.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+9402C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842760 | ||||||
| chr22:41842905
|
G | A | 6 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+9547G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842905 | ||||||
| chr22:41842986
|
G | A | 2 | a0002c0005t0006g0013a0002c0005t0007g0012 | 2 | HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.88+9628G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842986 | ||||||
| chr22:41842987
|
T | A | 1 | a0005c0006t0004g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88+9629T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41842987 | ||||||
| chr22:41842990
|
C | CA | 10 | a0001c0001t0001g0175a0002c0002t0002g0047a0002c0002t0002g0108others(7): Show | 10 | HG01243.hp2 HG02559.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+9646dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41842990 | |||||
| chr22:41842990
|
CA | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0317a0002c0002t0001g0118others(12): Show | 15 | HG01517.hp2 NA18951.hp2 NA18965.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+9646delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41842990 | |||||
| chr22:41843218
|
C | T | 19 | a0002c0002t0003g0008a0002c0002t0003g0055a0002c0002t0003g0056others(16): Show | 19 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+9860C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843218 | ||||||
| chr22:41843344
|
G | C | 70 | a0001c0001t0001g0005a0001c0001t0001g0126a0002c0002t0001g0002others(67): Show | 71 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.88+9986G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843344 | ||||||
| chr22:41843530
|
G | A | 3 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040 | 3 | HG01934.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.88+10172G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843530 | ||||||
| chr22:41843536
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0305 | 2 | NA18988.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.88+10178G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843536 | ||||||
| chr22:41843641
|
AAGTTGCA others(6): Show |
A | 1 | a0001c0001t0001g0270 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.88+10286_88+10298d others(15): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41843641 | |||||
| chr22:41843823
|
C | T | 55 | a0001c0001t0001g0070a0001c0001t0001g0094a0002c0002t0001g0106others(52): Show | 56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.88+10465C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843823 | ||||||
| chr22:41843934
|
T | C | 82 | a0001c0001t0001g0162a0001c0001t0001g0253a0001c0001t0001g0254others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.88+10576T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41843934 | ||||||
| chr22:41844015
|
C | CA | 59 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0165others(56): Show | 60 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.88+10670dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844015 | |||||
| chr22:41844027
|
A | AAATACAC others(4): Show |
1 | a0002c0002t0002g0149 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.88+10670_88+10671i others(13): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844027 | |||||
| chr22:41844027
|
A | AAATACAC others(8): Show |
1 | a0002c0002t0002g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.88+10670_88+10671i others(17): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844027 | |||||
| chr22:41844029
|
T | C | 2 | a0002c0002t0002g0147a0002c0002t0002g0149 | 2 | HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.88+10671T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844029 | ||||||
| chr22:41844029
|
T | TACACAC | 5 | a0001c0001t0008g0112a0002c0002t0002g0104a0006c0008t0003g0113others(2): Show | 5 | HG01346.hp1 HG02109.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+10674_88+10675i others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844029 | |||||
| chr22:41844029
|
TACATACA others(3): Show |
T | 1 | a0002c0002t0003g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.88+10675_88+10684d others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844029 | |||||
| chr22:41844029
|
TACATACA others(5): Show |
T | 1 | a0002c0002t0003g0053 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.88+10675_88+10686d others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844029 | |||||
| chr22:41844033
|
T | C | 72 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0008g0112others(69): Show | 73 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.88+10675T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844033 | ||||||
| chr22:41844033
|
T | TAC | 62 | a0001c0001t0001g0003a0001c0001t0001g0165a0001c0001t0001g0166others(59): Show | 63 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.88+10706_88+10707d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | |||||
| chr22:41844033
|
T | TACAC | 4 | a0001c0001t0001g0205a0001c0001t0001g0230a0002c0002t0002g0061others(1): Show | 4 | HG00673.hp2 HG03490.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+10704_88+10707d others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | |||||
| chr22:41844033
|
T | TACACAC | 32 | a0001c0001t0001g0070a0002c0002t0001g0106a0002c0002t0001g0107others(29): Show | 33 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.88+10702_88+10707d others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | |||||
| chr22:41844033
|
T | TACACACA others(1): Show |
17 | a0001c0001t0001g0094a0001c0001t0001g0270a0001c0001t0001g0298others(14): Show | 17 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.88+10700_88+10707d others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | |||||
| chr22:41844033
|
T | TACACACA others(3): Show |
52 | a0001c0001t0001g0162a0001c0001t0001g0254a0001c0001t0001g0255others(49): Show | 52 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(49): Show |
intron_variant | MODIFIER | c.88+10698_88+10707d others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | |||||
| chr22:41844033
|
T | TACACACA others(5): Show |
20 | a0001c0001t0001g0253a0001c0001t0001g0256a0001c0001t0001g0264others(17): Show | 20 | HG00733.hp2 HG01069.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+10696_88+10707d others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | |||||
| chr22:41844033
|
T | TACACACA others(7): Show |
1 | a0002c0002t0009g0322 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.88+10694_88+10707d others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | |||||
| chr22:41844033
|
TACACACA others(11): Show |
T | 1 | a0002c0016t0002g0083 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.88+10690_88+10707d others(20): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844033 | |||||
| chr22:41844048
|
A | ACACACAC others(3): Show |
2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG01106.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.88+10699_88+10700i others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41844048 | |||||
| chr22:41844065
|
C | CACACACA others(7): Show |
5 | a0002c0002t0002g0117a0002c0002t0002g0148a0003c0003t0004g0122others(2): Show | 5 | HG00642.hp2 HG03831.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | ||||||
| chr22:41844065
|
C | CACACACA others(5): Show |
4 | a0002c0002t0001g0150a0002c0002t0003g0329a0002c0002t0003g0330others(1): Show | 4 | HG03942.hp1 NA19003.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | ||||||
| chr22:41844065
|
C | CACACACA others(3): Show |
30 | a0001c0001t0001g0126a0002c0002t0001g0002a0002c0002t0001g0118others(27): Show | 31 | HG00099.hp1 HG01169.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | ||||||
| chr22:41844065
|
C | CACACACA others(1): Show |
48 | a0001c0001t0001g0005a0001c0001t0003g0010a0001c0001t0005g0018others(45): Show | 48 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | ||||||
| chr22:41844065
|
C | CACACAT | 9 | a0002c0002t0001g0039a0002c0002t0001g0040a0002c0002t0001g0121others(6): Show | 9 | HG01934.hp1 HG01943.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | ||||||
| chr22:41844065
|
C | CACAT | 5 | a0002c0002t0001g0037a0002c0002t0001g0146a0002c0002t0002g0036others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+10707_88+10708i others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | ||||||
| chr22:41844065
|
C | T | 5 | a0002c0002t0003g0052a0002c0002t0003g0053a0002c0005t0006g0013others(2): Show | 5 | HG02486.hp1 HG02886.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+10707C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844065 | ||||||
| chr22:41844340
|
G | T | 1 | a0002c0005t0007g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.88+10982G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844340 | ||||||
| chr22:41844429
|
C | T | 1 | a0002c0005t0007g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.88+11071C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844429 | ||||||
| chr22:41844614
|
C | T | 1 | a0002c0002t0001g0157 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.88+11256C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844614 | ||||||
| chr22:41844625
|
G | A | 3 | a0004c0004t0003g0004a0004c0004t0011g0043a0004c0004t0011g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+11267G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844625 | ||||||
| chr22:41844672
|
G | C | 3 | a0004c0004t0003g0004a0004c0004t0011g0043a0004c0004t0011g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.88+11314G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844672 | ||||||
| chr22:41844793
|
C | T | 254 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.88+11435C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844793 | ||||||
| chr22:41844903
|
G | C | 1 | a0004c0004t0006g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.88+11545G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41844903 | ||||||
| chr22:41845158
|
T | G | 1 | a0002c0002t0002g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.88+11800T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845158 | ||||||
| chr22:41845198
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.88+11840C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845198 | ||||||
| chr22:41845368
|
G | A | 67 | a0001c0001t0001g0005a0001c0001t0001g0126a0002c0002t0001g0002others(64): Show | 68 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.88+12010G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845368 | ||||||
| chr22:41845391
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.88+12033G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845391 | ||||||
| chr22:41845454
|
T | A | 1 | a0005c0006t0004g0241 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.88+12096T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845454 | ||||||
| chr22:41845779
|
T | A | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.88+12421T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41845779 | ||||||
| chr22:41846031
|
T | A | 6 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+12673T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41846031 | ||||||
| chr22:41846053
|
G | T | 12 | a0001c0001t0003g0010a0001c0001t0005g0018a0002c0002t0005g0014others(9): Show | 12 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+12695G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41846053 | ||||||
| chr22:41846494
|
C | T | 1 | a0002c0002t0002g0028 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.88+13136C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41846494 | ||||||
| chr22:41847016
|
T | C | 255 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.88+13658T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847016 | ||||||
| chr22:41847517
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.88+14159G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847517 | ||||||
| chr22:41847578
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.88+14220G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847578 | ||||||
| chr22:41847614
|
T | C | 77 | a0001c0001t0001g0162a0001c0001t0001g0253a0001c0001t0001g0254others(74): Show | 77 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.88+14256T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847614 | ||||||
| chr22:41847837
|
T | C | 101 | a0001c0001t0001g0162a0001c0001t0001g0253a0001c0001t0001g0254others(98): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.88+14479T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847837 | ||||||
| chr22:41847838
|
A | T | 3 | a0001c0001t0003g0306a0001c0001t0003g0309a0001c0001t0003g0310 | 3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.88+14480A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847838 | ||||||
| chr22:41847917
|
A | AT | 19 | a0001c0001t0005g0018a0002c0002t0002g0078a0002c0002t0002g0079others(16): Show | 19 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.88+14561dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41847917 | |||||
| chr22:41847920
|
A | AT | 159 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0162others(156): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.88+14575dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41847920 | |||||
| chr22:41847920
|
A | T | 22 | a0001c0001t0001g0200a0001c0001t0001g0216a0001c0001t0003g0010others(19): Show | 22 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.88+14562A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847920 | ||||||
| chr22:41847922
|
T | TA | 73 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0279others(70): Show | 73 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.88+14564_88+14565i others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847922 | ||||||
| chr22:41847925
|
T | A | 5 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040others(2): Show | 5 | HG01934.hp1 HG01943.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+14567T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41847925 | ||||||
| chr22:41848030
|
C | G | 22 | a0001c0001t0003g0306a0001c0001t0003g0309a0001c0001t0003g0310others(19): Show | 22 | HG01433.hp1 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.88+14672C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848030 | ||||||
| chr22:41848137
|
C | T | 1 | a0002c0005t0007g0248 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+14779C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848137 | ||||||
| chr22:41848190
|
C | T | 1 | a0002c0002t0005g0019 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88+14832C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848190 | ||||||
| chr22:41848208
|
G | A | 55 | a0001c0001t0001g0070a0001c0001t0001g0094a0002c0002t0001g0106others(52): Show | 56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.88+14850G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848208 | ||||||
| chr22:41848379
|
G | A | 13 | a0001c0001t0001g0070a0002c0002t0001g0106a0002c0002t0001g0107others(10): Show | 14 | HG00597.hp2 HG00621.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.88+15021G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848379 | ||||||
| chr22:41848548
|
C | T | 1 | a0002c0002t0002g0081 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.88+15190C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848548 | ||||||
| chr22:41848841
|
G | T | 3 | a0002c0002t0001g0144a0003c0003t0004g0134a0003c0003t0004g0135 | 3 | HG00099.hp1 NA20300.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.88+15483G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41848841 | ||||||
| chr22:41849269
|
G | C | 1 | a0002c0002t0001g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.88+15911G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849269 | ||||||
| chr22:41849510
|
C | G | 5 | a0001c0007t0003g0007a0001c0007t0003g0086a0001c0007t0003g0087others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+16152C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849510 | ||||||
| chr22:41849718
|
G | T | 62 | a0001c0001t0001g0005a0002c0002t0001g0002a0002c0002t0001g0029others(59): Show | 63 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.88+16360G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849718 | ||||||
| chr22:41849759
|
C | T | 253 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+16401C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849759 | ||||||
| chr22:41849863
|
G | T | 1 | a0001c0001t0005g0018 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.88+16505G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849863 | ||||||
| chr22:41849940
|
C | CATCAGGA others(1): Show |
145 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(142): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.88+16585_88+16586i others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41849940 | |||||
| chr22:41849944
|
C | G | 145 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(142): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.88+16586C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849944 | ||||||
| chr22:41849945
|
T | A | 145 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(142): Show | 147 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.88+16587T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849945 | ||||||
| chr22:41849962
|
C | A | 6 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+16604C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849962 | ||||||
| chr22:41849966
|
A | G | 253 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.88+16608A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41849966 | ||||||
| chr22:41850033
|
G | A | 55 | a0001c0001t0001g0070a0001c0001t0001g0094a0002c0002t0001g0106others(52): Show | 56 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.88+16675G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850033 | ||||||
| chr22:41850046
|
G | A | 1 | a0002c0002t0006g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.88+16688G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850046 | ||||||
| chr22:41850091
|
G | T | 12 | a0001c0001t0003g0010a0001c0001t0005g0018a0002c0002t0005g0014others(9): Show | 12 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.88+16733G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850091 | ||||||
| chr22:41850307
|
G | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | NA18950.hp2 NA18982.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.89-16524G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850307 | ||||||
| chr22:41850388
|
C | T | 253 | a0001c0001t0001g0005a0001c0001t0001g0070a0001c0001t0001g0094others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.89-16443C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850388 | ||||||
| chr22:41850449
|
C | CA | 66 | a0001c0001t0001g0005a0001c0001t0001g0165a0001c0001t0001g0231others(63): Show | 67 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.89-16367dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41850449 | |||||
| chr22:41850503
|
C | T | 7 | a0002c0002t0002g0047a0002c0002t0002g0108a0004c0004t0001g0042others(4): Show | 7 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-16328C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850503 | ||||||
| chr22:41850560
|
T | A | 26 | a0002c0002t0002g0047a0002c0002t0002g0108a0002c0002t0003g0008others(23): Show | 26 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.89-16271T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850560 | ||||||
| chr22:41850665
|
C | A | 1 | a0002c0002t0006g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-16166C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41850665 | ||||||
| chr22:41850750
|
CTTTTTG | C | 82 | a0001c0001t0001g0162a0001c0001t0001g0253a0001c0001t0001g0254others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.89-16075_89-16070d others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41850750 | |||||
| chr22:41851144
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0017g0197 | 2 | HG00597.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.89-15687A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851144 | ||||||
| chr22:41851356
|
G | A | 79 | a0001c0001t0001g0162a0001c0001t0001g0253a0001c0001t0001g0254others(76): Show | 79 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.89-15475G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851356 | ||||||
| chr22:41851379
|
A | G | 5 | a0002c0002t0002g0047a0002c0002t0002g0108a0004c0004t0010g0044others(2): Show | 5 | HG02559.hp2 HG02572.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-15452A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851379 | ||||||
| chr22:41851487
|
TTTTG | T | 5 | a0001c0001t0001g0168a0001c0001t0001g0192a0001c0001t0001g0193others(2): Show | 5 | HG00423.hp1 HG00558.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-15328_89-15325d others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41851487 | |||||
| chr22:41851499
|
G | GT | 62 | a0001c0001t0001g0005a0002c0002t0001g0002a0002c0002t0001g0029others(59): Show | 63 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.89-15329dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41851499 | |||||
| chr22:41851503
|
G | GT | 24 | a0001c0001t0003g0010a0001c0001t0004g0245a0001c0001t0005g0018others(21): Show | 24 | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.89-15321dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41851503 | |||||
| chr22:41851503
|
G | T | 74 | a0001c0001t0001g0005a0002c0002t0001g0002a0002c0002t0001g0029others(71): Show | 75 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.89-15328G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851503 | ||||||
| chr22:41851605
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.89-15226T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851605 | ||||||
| chr22:41851691
|
C | T | 78 | a0001c0001t0001g0162a0001c0001t0001g0253a0001c0001t0001g0254others(75): Show | 78 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.89-15140C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851691 | ||||||
| chr22:41851762
|
T | G | 1 | a0001c0001t0003g0010 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.89-15069T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851762 | ||||||
| chr22:41851800
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-15031G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851800 | ||||||
| chr22:41851823
|
A | C | 1 | a0002c0002t0002g0073 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.89-15008A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851823 | ||||||
| chr22:41851928
|
G | A | 240 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0126others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.89-14903G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851928 | ||||||
| chr22:41851948
|
G | A | 6 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-14883G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851948 | ||||||
| chr22:41851980
|
G | A | 10 | a0001c0001t0001g0094a0001c0001t0001g0271a0002c0002t0002g0009others(7): Show | 10 | HG00323.hp2 HG01069.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-14851G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41851980 | ||||||
| chr22:41852086
|
A | G | 3 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0324 | 3 | HG01109.hp2 HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.89-14745A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852086 | ||||||
| chr22:41852126
|
A | G | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG01081.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.89-14705A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852126 | ||||||
| chr22:41852177
|
G | A | 28 | a0002c0002t0002g0047a0002c0002t0002g0108a0002c0002t0003g0008others(25): Show | 28 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.89-14654G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852177 | ||||||
| chr22:41852278
|
A | G | 15 | a0002c0002t0003g0008a0002c0002t0003g0055a0002c0002t0003g0056others(12): Show | 15 | HG01884.hp1 HG02280.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.89-14553A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852278 | ||||||
| chr22:41852285
|
C | T | 2 | a0001c0001t0001g0318a0001c0001t0015g0319 | 2 | HG00639.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.89-14546C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852285 | ||||||
| chr22:41852351
|
T | A | 1 | a0002c0002t0001g0161 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.89-14480T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852351 | ||||||
| chr22:41852354
|
A | T | 1 | a0002c0002t0001g0161 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.89-14477A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852354 | ||||||
| chr22:41852359
|
A | C | 1 | a0002c0002t0001g0161 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.89-14472A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852359 | ||||||
| chr22:41852368
|
A | T | 1 | a0002c0002t0001g0161 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.89-14463A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852368 | ||||||
| chr22:41852520
|
G | A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-14311G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852520 | ||||||
| chr22:41852728
|
A | AT | 36 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0009others(33): Show | 36 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.89-14072dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | |||||
| chr22:41852728
|
A | ATT | 21 | a0001c0001t0001g0094a0002c0002t0002g0027a0002c0002t0002g0062others(18): Show | 21 | HG00323.hp2 HG00735.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.89-14073_89-14072d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | |||||
| chr22:41852728
|
AT | A | 69 | a0001c0001t0001g0165a0001c0001t0001g0169a0001c0001t0001g0170others(66): Show | 69 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.89-14072delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | |||||
| chr22:41852728
|
ATT | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0126others(81): Show | 86 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.89-14073_89-14072d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | |||||
| chr22:41852728
|
ATTT | A | 53 | a0001c0001t0001g0070a0001c0001t0001g0162a0001c0001t0001g0180others(50): Show | 53 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.89-14074_89-14072d others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | |||||
| chr22:41852728
|
ATTTTTTT others(1): Show |
A | 6 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0002g0047others(3): Show | 6 | HG01884.hp1 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-14079_89-14072d others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | |||||
| chr22:41852728
|
ATTTTTTT others(2): Show |
A | 32 | a0002c0002t0001g0029a0002c0002t0001g0032a0002c0002t0001g0033others(29): Show | 32 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.89-14080_89-14072d others(11): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | |||||
| chr22:41852728
|
ATTTTTTT others(3): Show |
A | 1 | a0004c0004t0011g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.89-14081_89-14072d others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | |||||
| chr22:41852728
|
ATTTTTTT others(10): Show |
A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-14088_89-14072d others(19): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41852728 | |||||
| chr22:41852817
|
A | G | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-14014A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852817 | ||||||
| chr22:41852856
|
G | A | 257 | a0001c0001t0001g0162a0001c0001t0001g0231a0001c0001t0001g0238others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.89-13975G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852856 | ||||||
| chr22:41852889
|
G | T | 1 | a0001c0001t0001g0291 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-13942G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852889 | ||||||
| chr22:41852911
|
A | G | 1 | a0002c0002t0003g0330 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.89-13920A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852911 | ||||||
| chr22:41852969
|
C | T | 3 | a0004c0004t0003g0004a0004c0004t0011g0043a0004c0004t0011g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.89-13862C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41852969 | ||||||
| chr22:41853493
|
A | G | 1 | a0001c0012t0001g0312 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.89-13338A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853493 | ||||||
| chr22:41853525
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.89-13306A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853525 | ||||||
| chr22:41853603
|
GT | G | 3 | a0004c0004t0003g0004a0004c0004t0011g0043a0004c0004t0011g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.89-13227delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853603 | ||||||
| chr22:41853927
|
C | T | 39 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-12904C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853927 | ||||||
| chr22:41853939
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-12892G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853939 | ||||||
| chr22:41853951
|
C | T | 4 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0322others(1): Show | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-12880C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853951 | ||||||
| chr22:41853991
|
C | T | 31 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-12840C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41853991 | ||||||
| chr22:41854021
|
C | T | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-12810C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854021 | ||||||
| chr22:41854130
|
TTTG | T | 60 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.89-12689_89-12687d others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41854130 | |||||
| chr22:41854288
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.89-12543A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854288 | ||||||
| chr22:41854395
|
C | G | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-12436C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854395 | ||||||
| chr22:41854503
|
C | T | 2 | a0002c0002t0003g0024a0002c0002t0003g0026 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.89-12328C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854503 | ||||||
| chr22:41854565
|
C | CT | 39 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-12263dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41854565 | |||||
| chr22:41854726
|
G | A | 1 | a0004c0004t0003g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.89-12105G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854726 | ||||||
| chr22:41854794
|
G | T | 2 | a0001c0001t0012g0178a0001c0001t0020g0179 | 2 | HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.89-12037G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854794 | ||||||
| chr22:41854798
|
G | T | 2 | a0001c0001t0012g0178a0001c0001t0020g0179 | 2 | HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.89-12033G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854798 | ||||||
| chr22:41854802
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0205others(2): Show | 5 | HG00673.hp2 NA18953.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-12029G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854802 | ||||||
| chr22:41854894
|
A | G | 6 | a0002c0002t0003g0008a0002c0002t0003g0055a0002c0002t0003g0056others(3): Show | 6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-11937A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854894 | ||||||
| chr22:41854988
|
G | A | 2 | a0001c0012t0001g0312a0001c0012t0001g0313 | 2 | HG01358.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.89-11843G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854988 | ||||||
| chr22:41854999
|
C | T | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-11832C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41854999 | ||||||
| chr22:41855019
|
T | TA | 7 | a0001c0001t0001g0184a0001c0001t0001g0263a0001c0001t0001g0264others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-11796dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855019 | |||||
| chr22:41855019
|
T | TAA | 51 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(48): Show | 52 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.89-11797_89-11796d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855019 | |||||
| chr22:41855019
|
TA | T | 7 | a0002c0002t0003g0052a0002c0002t0003g0053a0002c0005t0006g0249others(4): Show | 7 | HG02451.hp1 HG02486.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-11796delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855019 | |||||
| chr22:41855032
|
A | C | 1 | a0004c0004t0003g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.89-11799A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855032 | ||||||
| chr22:41855049
|
A | C | 39 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-11782A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855049 | ||||||
| chr22:41855064
|
T | G | 1 | a0002c0002t0005g0017 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.89-11767T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855064 | ||||||
| chr22:41855119
|
T | C | 56 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(53): Show | 57 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.89-11712T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855119 | ||||||
| chr22:41855186
|
T | A | 51 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(48): Show | 52 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.89-11645T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855186 | ||||||
| chr22:41855397
|
G | A | 1 | a0004c0004t0011g0043 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.89-11434G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855397 | ||||||
| chr22:41855432
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-11399G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855432 | ||||||
| chr22:41855521
|
C | CA | 5 | a0001c0001t0001g0236a0001c0001t0001g0280a0001c0001t0003g0210others(2): Show | 5 | HG00140.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-11302dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855521 | |||||
| chr22:41855754
|
A | C | 3 | a0001c0001t0003g0306a0001c0001t0003g0309a0001c0001t0003g0310 | 3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.89-11077A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855754 | ||||||
| chr22:41855755
|
C | CT | 10 | a0001c0001t0001g0190a0001c0001t0002g0257a0002c0002t0001g0029others(7): Show | 10 | HG00423.hp2 HG00733.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-11059dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855755 | |||||
| chr22:41855755
|
CT | C | 68 | a0001c0001t0001g0209a0001c0001t0001g0232a0001c0001t0001g0238others(65): Show | 69 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.89-11059delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41855755 | |||||
| chr22:41855806
|
G | T | 82 | a0001c0001t0001g0162a0001c0001t0001g0231a0001c0001t0001g0238others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.89-11025G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855806 | ||||||
| chr22:41855909
|
C | T | 1 | a0002c0002t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.89-10922C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855909 | ||||||
| chr22:41855913
|
G | C | 12 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(9): Show | 12 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.89-10918G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855913 | ||||||
| chr22:41855957
|
A | G | 2 | a0002c0009t0002g0208a0002c0009t0002g0226 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.89-10874A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41855957 | ||||||
| chr22:41856090
|
G | GT | 6 | a0002c0002t0003g0328a0002c0002t0003g0329a0002c0002t0003g0330others(3): Show | 6 | HG02630.hp1 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-10732dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41856090 | |||||
| chr22:41856176
|
G | A | 39 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-10655G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856176 | ||||||
| chr22:41856212
|
C | T | 1 | a0002c0002t0001g0129 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.89-10619C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856212 | ||||||
| chr22:41856223
|
C | T | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-10608C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856223 | ||||||
| chr22:41856252
|
G | A | 1 | a0002c0005t0007g0250 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.89-10579G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856252 | ||||||
| chr22:41856413
|
G | A | 4 | a0005c0006t0004g0119a0005c0006t0004g0124a0005c0006t0004g0132others(1): Show | 4 | NA18942.hp1 NA18978.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-10418G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856413 | ||||||
| chr22:41856585
|
C | G | 48 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(45): Show | 49 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.89-10246C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856585 | ||||||
| chr22:41856803
|
G | A | 1 | a0002c0002t0002g0075 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.89-10028G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856803 | ||||||
| chr22:41856823
|
C | G | 2 | a0002c0002t0002g0074a0002c0002t0002g0104 | 2 | HG01167.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.89-10008C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856823 | ||||||
| chr22:41856890
|
C | G | 60 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.89-9941C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856890 | ||||||
| chr22:41856956
|
A | G | 60 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.89-9875A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856956 | ||||||
| chr22:41856958
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.89-9873A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856958 | ||||||
| chr22:41856971
|
A | T | 2 | a0001c0001t0001g0277a0001c0001t0001g0291 | 2 | NA18979.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.89-9860A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41856971 | ||||||
| chr22:41857021
|
C | T | 1 | a0002c0002t0001g0143 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.89-9810C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857021 | ||||||
| chr22:41857042
|
G | A | 1 | a0003c0003t0004g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.89-9789G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857042 | ||||||
| chr22:41857066
|
C | CA | 73 | a0001c0001t0001g0189a0001c0001t0001g0253a0001c0001t0001g0279others(70): Show | 74 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.89-9749dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41857066 | |||||
| chr22:41857066
|
C | CAA | 79 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(76): Show | 80 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.89-9750_89-9749dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41857066 | |||||
| chr22:41857447
|
G | A | 1 | a0004c0004t0001g0227 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.89-9384G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857447 | ||||||
| chr22:41857585
|
G | A | 3 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0012g0213 | 3 | HG01517.hp1 HG01943.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.89-9246G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857585 | ||||||
| chr22:41857708
|
C | T | 1 | a0002c0002t0003g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.89-9123C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857708 | ||||||
| chr22:41857723
|
G | A | 48 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(45): Show | 49 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.89-9108G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857723 | ||||||
| chr22:41857759
|
C | T | 48 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(45): Show | 49 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.89-9072C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857759 | ||||||
| chr22:41857823
|
T | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0228 | 2 | HG00673.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.89-9008T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41857823 | ||||||
| chr22:41858048
|
G | T | 2 | a0001c0001t0001g0175a0001c0001t0001g0183 | 2 | NA18952.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.89-8783G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858048 | ||||||
| chr22:41858086
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0013g0220 | 2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.89-8745G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858086 | ||||||
| chr22:41858121
|
C | T | 1 | a0002c0002t0001g0120 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.89-8710C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858121 | ||||||
| chr22:41858196
|
G | C | 1 | a0001c0001t0001g0162 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.89-8635G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858196 | ||||||
| chr22:41858355
|
A | G | 3 | a0005c0006t0004g0119a0005c0006t0004g0132a0005c0006t0004g0133 | 3 | NA18978.hp2 NA19004.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.89-8476A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858355 | ||||||
| chr22:41858517
|
A | AGG | 39 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-8313_89-8312dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41858517 | |||||
| chr22:41858812
|
T | C | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-8019T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858812 | ||||||
| chr22:41858846
|
A | T | 2 | a0003c0003t0004g0122a0003c0003t0004g0123 | 2 | NA18939.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.89-7985A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858846 | ||||||
| chr22:41858914
|
C | T | 1 | a0002c0002t0002g0104 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.89-7917C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858914 | ||||||
| chr22:41858926
|
G | A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-7905G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858926 | ||||||
| chr22:41858984
|
G | T | 5 | a0001c0007t0003g0007a0001c0007t0003g0086a0001c0007t0003g0087others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-7847G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41858984 | ||||||
| chr22:41859145
|
G | A | 1 | a0003c0003t0004g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.89-7686G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859145 | ||||||
| chr22:41859371
|
A | T | 1 | a0001c0001t0001g0276 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.89-7460A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859371 | ||||||
| chr22:41859521
|
A | G | 250 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(247): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.89-7310A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859521 | ||||||
| chr22:41859701
|
A | G | 51 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(48): Show | 52 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.89-7130A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859701 | ||||||
| chr22:41859709
|
G | C | 1 | a0002c0002t0006g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-7122G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859709 | ||||||
| chr22:41859799
|
C | CT | 94 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0094others(91): Show | 95 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.89-7003dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | |||||
| chr22:41859799
|
C | CTT | 37 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0167others(34): Show | 37 | HG00558.hp1 HG00733.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.89-7004_89-7003dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | |||||
| chr22:41859799
|
CT | C | 38 | a0002c0002t0001g0120a0002c0002t0001g0121a0002c0002t0001g0127others(35): Show | 38 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.89-7003delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | |||||
| chr22:41859799
|
CTT | C | 16 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0040others(13): Show | 16 | HG01943.hp1 HG02559.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-7004_89-7003del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | |||||
| chr22:41859799
|
CTTT | C | 28 | a0002c0002t0001g0029a0002c0002t0001g0032a0002c0002t0001g0033others(25): Show | 28 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.89-7005_89-7003del others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | |||||
| chr22:41859799
|
CTTTTTTT others(6): Show |
C | 1 | a0002c0002t0002g0104 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.89-7015_89-7003del others(13): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41859799 | |||||
| chr22:41859941
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-6890G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859941 | ||||||
| chr22:41859963
|
G | A | 1 | a0002c0002t0009g0322 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.89-6868G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859963 | ||||||
| chr22:41859988
|
G | A | 6 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-6843G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41859988 | ||||||
| chr22:41860052
|
G | A | 3 | a0001c0001t0003g0306a0001c0001t0003g0309a0001c0001t0003g0310 | 3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.89-6779G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860052 | ||||||
| chr22:41860084
|
T | C | 322 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(319): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.89-6747T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860084 | ||||||
| chr22:41860207
|
G | A | 1 | a0008c0014t0006g0023 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.89-6624G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860207 | ||||||
| chr22:41860241
|
GA | G | 41 | a0001c0001t0001g0232a0001c0001t0013g0220a0002c0002t0001g0029others(38): Show | 41 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-6577delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41860241 | |||||
| chr22:41860431
|
T | C | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-6400T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860431 | ||||||
| chr22:41860520
|
A | T | 1 | a0002c0002t0002g0028 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.89-6311A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860520 | ||||||
| chr22:41860535
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.89-6296A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860535 | ||||||
| chr22:41860810
|
C | T | 48 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(45): Show | 49 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.89-6021C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41860810 | ||||||
| chr22:41861017
|
G | A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-5814G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861017 | ||||||
| chr22:41861206
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-5625G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861206 | ||||||
| chr22:41861259
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.89-5572G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861259 | ||||||
| chr22:41861641
|
G | A | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-5190G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861641 | ||||||
| chr22:41861664
|
T | G | 1 | a0001c0001t0001g0268 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.89-5167T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861664 | ||||||
| chr22:41861689
|
G | A | 39 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-5142G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861689 | ||||||
| chr22:41861790
|
G | T | 1 | a0002c0002t0001g0039 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.89-5041G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41861790 | ||||||
| chr22:41862011
|
C | T | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4820C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862011 | ||||||
| chr22:41862012
|
C | A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4819C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862012 | ||||||
| chr22:41862013
|
C | T | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4818C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862013 | ||||||
| chr22:41862018
|
C | G | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4813C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862018 | ||||||
| chr22:41862019
|
C | T | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4812C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862019 | ||||||
| chr22:41862026
|
G | GTATTTAA others(6): Show |
2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4805_89-4804ins others(13): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862026 | ||||||
| chr22:41862028
|
C | G | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4803C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862028 | ||||||
| chr22:41862030
|
G | A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4801G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862030 | ||||||
| chr22:41862031
|
G | T | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4800G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862031 | ||||||
| chr22:41862032
|
G | T | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-4799G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862032 | ||||||
| chr22:41862045
|
G | A | 250 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(247): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.89-4786G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862045 | ||||||
| chr22:41862268
|
G | A | 39 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-4563G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862268 | ||||||
| chr22:41862333
|
G | C | 1 | a0002c0002t0006g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-4498G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862333 | ||||||
| chr22:41862440
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-4391G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862440 | ||||||
| chr22:41862442
|
G | T | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-4389G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862442 | ||||||
| chr22:41862573
|
C | G | 59 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(56): Show | 60 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-4258C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862573 | ||||||
| chr22:41862655
|
A | G | 2 | a0002c0002t0001g0121a0002c0002t0001g0157 | 2 | NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.89-4176A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862655 | ||||||
| chr22:41862756
|
G | A | 1 | a0002c0015t0002g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.89-4075G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862756 | ||||||
| chr22:41862836
|
C | T | 6 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(3): Show | 6 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3995C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41862836 | ||||||
| chr22:41863094
|
C | T | 250 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(247): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.89-3737C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863094 | ||||||
| chr22:41863112
|
G | A | 1 | a0002c0005t0007g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.89-3719G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863112 | ||||||
| chr22:41863504
|
A | G | 1 | a0003c0003t0004g0141 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.89-3327A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863504 | ||||||
| chr22:41863520
|
C | G | 5 | a0002c0002t0001g0136a0002c0002t0001g0142a0002c0002t0001g0143others(2): Show | 5 | HG00621.hp2 NA18747.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-3311C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863520 | ||||||
| chr22:41863520
|
C | T | 6 | a0001c0001t0001g0209a0001c0001t0001g0214a0001c0001t0001g0215others(3): Show | 6 | HG00733.hp1 HG01258.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3311C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863520 | ||||||
| chr22:41863648
|
A | G | 6 | a0002c0002t0003g0008a0002c0002t0003g0055a0002c0002t0003g0056others(3): Show | 6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3183A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863648 | ||||||
| chr22:41863680
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0228 | 2 | HG00673.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.89-3151G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863680 | ||||||
| chr22:41863860
|
C | CATTT | 18 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.89-2960_89-2957dup others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41863860 | |||||
| chr22:41863904
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.89-2927C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863904 | ||||||
| chr22:41863905
|
G | A | 4 | a0005c0006t0004g0119a0005c0006t0004g0124a0005c0006t0004g0132others(1): Show | 4 | NA18942.hp1 NA18978.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2926G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41863905 | ||||||
| chr22:41864165
|
C | T | 39 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.89-2666C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864165 | ||||||
| chr22:41864223
|
C | CAT | 42 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0165others(39): Show | 43 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.89-2570_89-2569dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
C | CATAT | 27 | a0001c0001t0001g0172a0001c0001t0001g0253a0001c0001t0001g0264others(24): Show | 27 | HG00642.hp1 HG01175.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-2572_89-2569dup others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
C | CATATAT | 32 | a0001c0001t0001g0126a0001c0001t0001g0167a0001c0001t0001g0175others(29): Show | 32 | HG00099.hp2 HG00558.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.89-2574_89-2569dup others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
C | CATATATA others(1): Show |
31 | a0001c0001t0001g0070a0001c0001t0001g0190a0001c0001t0001g0205others(28): Show | 31 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-2576_89-2569dup others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
C | CATATATA others(3): Show |
1 | a0005c0021t0001g0261 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.89-2578_89-2569dup others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
C | CATATATA others(9): Show |
2 | a0002c0002t0002g0061a0002c0002t0002g0077 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.89-2584_89-2569dup others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
C | CATATATA others(11): Show |
1 | a0001c0001t0001g0325 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.89-2586_89-2569dup others(18): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
CAT | C | 8 | a0001c0001t0001g0255a0001c0001t0001g0272a0001c0001t0001g0305others(5): Show | 8 | HG01106.hp1 HG02129.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-2570_89-2569del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
CATATATA others(3): Show |
C | 5 | a0001c0001t0001g0094a0001c0001t0001g0232a0001c0001t0001g0235others(2): Show | 5 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-2578_89-2569del others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
CATATATA others(5): Show |
C | 4 | a0001c0001t0001g0219a0001c0001t0001g0230a0001c0001t0001g0234others(1): Show | 4 | HG00140.hp1 HG00735.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2580_89-2569del others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
CATATATA others(7): Show |
C | 5 | a0001c0001t0001g0233a0001c0001t0008g0112a0006c0008t0003g0113others(2): Show | 5 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2582_89-2569del others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864223
|
CATATATA others(9): Show |
C | 2 | a0001c0001t0008g0243a0001c0001t0008g0244 | 2 | HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.89-2584_89-2569del others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864223 | |||||
| chr22:41864249
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0001g0217 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.89-2580_89-2567del others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864249 | |||||
| chr22:41864251
|
TATATATA others(5): Show |
T | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(1): Show | 4 | HG01258.hp1 HG01517.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2578_89-2567del others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864251 | |||||
| chr22:41864251
|
TATATATA others(7): Show |
T | 1 | a0002c0002t0006g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89-2578_89-2565del others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864251 | |||||
| chr22:41864251
|
TATATATA others(9): Show |
T | 1 | a0002c0002t0005g0020 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-2578_89-2563del others(16): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864251 | |||||
| chr22:41864253
|
TATATATA others(3): Show |
T | 1 | a0001c0001t0001g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.89-2576_89-2567del others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864253 | |||||
| chr22:41864255
|
T | C | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.89-2576T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864255 | ||||||
| chr22:41864255
|
TATATATA others(1): Show |
T | 5 | a0002c0002t0002g0085a0002c0002t0002g0163a0002c0002t0003g0330others(2): Show | 5 | HG03017.hp2 HG03225.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-2574_89-2567del others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864255 | |||||
| chr22:41864255
|
TATATATA others(3): Show |
T | 9 | a0002c0002t0001g0029a0002c0002t0001g0031a0002c0002t0001g0032others(6): Show | 9 | HG00408.hp2 HG00423.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.89-2574_89-2565del others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864255 | |||||
| chr22:41864255
|
TATATATA others(5): Show |
T | 2 | a0002c0005t0006g0249a0002c0005t0007g0012 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.89-2574_89-2563del others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864255 | |||||
| chr22:41864257
|
T | C | 3 | a0002c0002t0003g0052a0002c0002t0003g0053a0003c0003t0004g0140 | 3 | HG02886.hp2 HG02897.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.89-2574T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864257 | ||||||
| chr22:41864257
|
T | TACAC | 3 | a0002c0002t0001g0127a0002c0002t0001g0160a0003c0003t0004g0141 | 3 | HG03704.hp1 NA18959.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.89-2573_89-2572ins others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | |||||
| chr22:41864257
|
T | TACACAC | 3 | a0002c0002t0001g0118a0002c0002t0001g0138a0002c0025t0001g0139 | 3 | NA18946.hp1 NA18979.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.89-2573_89-2572ins others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | |||||
| chr22:41864257
|
TATATAC | T | 29 | a0002c0002t0001g0037a0002c0002t0002g0025a0002c0002t0002g0027others(26): Show | 29 | HG00738.hp1 HG00741.hp2 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.89-2572_89-2567del others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | |||||
| chr22:41864257
|
TATATACA others(1): Show |
T | 3 | a0002c0002t0001g0030a0002c0002t0001g0033a0002c0002t0006g0048 | 3 | HG00673.hp1 HG02559.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.89-2572_89-2565del others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | |||||
| chr22:41864257
|
TATATACA others(3): Show |
T | 2 | a0002c0002t0005g0016a0002c0005t0006g0013 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.89-2572_89-2563del others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864257 | |||||
| chr22:41864259
|
T | C | 10 | a0002c0002t0001g0118a0002c0002t0001g0127a0002c0002t0001g0138others(7): Show | 10 | HG02886.hp2 HG02897.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-2572T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864259 | ||||||
| chr22:41864259
|
T | TACACAC | 17 | a0002c0002t0001g0120a0002c0002t0001g0121a0002c0002t0001g0136others(14): Show | 17 | HG01169.hp2 HG01981.hp1 HG03017.hp1 others(14): Show |
intron_variant | MODIFIER | c.89-2571_89-2570ins others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864259 | |||||
| chr22:41864259
|
T | TACACACA others(3): Show |
1 | a0005c0006t0004g0132 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.89-2571_89-2570ins others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864259 | |||||
| chr22:41864259
|
TATAC | T | 18 | a0002c0002t0001g0107a0002c0002t0002g0001a0002c0002t0002g0009others(15): Show | 19 | HG00280.hp2 HG00621.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.89-2570_89-2567del others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864259 | |||||
| chr22:41864259
|
TATACAC | T | 3 | a0002c0002t0002g0096a0002c0002t0002g0098a0003c0003t0004g0097 | 3 | HG01257.hp1 HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.89-2570_89-2565del others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864259 | |||||
| chr22:41864261
|
T | C | 31 | a0001c0001t0001g0094a0001c0001t0001g0162a0002c0002t0001g0118others(28): Show | 31 | HG00323.hp2 HG01169.hp2 HG01981.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-2570T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864261 | ||||||
| chr22:41864261
|
T | TACACACA others(1): Show |
5 | a0002c0002t0001g0002a0002c0002t0001g0131a0002c0002t0001g0144others(2): Show | 6 | HG00099.hp1 NA18945.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2554_89-2547dup others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | |||||
| chr22:41864261
|
T | TACACACA others(3): Show |
7 | a0002c0002t0001g0143a0002c0002t0001g0154a0003c0003t0004g0135others(4): Show | 7 | HG00621.hp2 HG01081.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2556_89-2547dup others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | |||||
| chr22:41864261
|
T | TATAC | 4 | a0001c0001t0001g0267a0001c0001t0001g0270a0001c0001t0001g0273others(1): Show | 4 | HG02293.hp1 NA18942.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2569_89-2568ins others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | |||||
| chr22:41864261
|
T | TATACACA others(3): Show |
5 | a0002c0002t0002g0117a0002c0002t0002g0147a0002c0002t0002g0148others(2): Show | 5 | HG00642.hp2 HG03225.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-2569_89-2568ins others(10): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | |||||
| chr22:41864261
|
T | TATACACA others(5): Show |
1 | a0002c0002t0001g0146 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.89-2569_89-2568ins others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | |||||
| chr22:41864261
|
T | TATATAC | 5 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0285others(2): Show | 5 | HG00639.hp1 HG02451.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-2569_89-2568ins others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | |||||
| chr22:41864261
|
T | TATATACA others(5): Show |
2 | a0002c0002t0001g0129a0002c0013t0001g0229 | 2 | HG02145.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.89-2569_89-2568ins others(12): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | |||||
| chr22:41864261
|
T | TATATACA others(7): Show |
1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-2569_89-2568ins others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | |||||
| chr22:41864261
|
TAC | T | 13 | a0001c0001t0001g0180a0002c0002t0002g0074a0002c0002t0002g0092others(10): Show | 13 | HG01167.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.89-2548_89-2547del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864261 | |||||
| chr22:41864263
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(78): Show | 82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.89-2568C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864263 | ||||||
| chr22:41864265
|
C | T | 12 | a0001c0001t0001g0200a0002c0002t0005g0014a0002c0002t0005g0015others(9): Show | 12 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.89-2566C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864265 | ||||||
| chr22:41864267
|
C | T | 65 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(62): Show | 66 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.89-2564C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864267 | ||||||
| chr22:41864269
|
C | T | 3 | a0002c0002t0002g0096a0002c0002t0002g0098a0003c0003t0004g0097 | 3 | HG01257.hp1 HG01258.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.89-2562C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864269 | ||||||
| chr22:41864295
|
ATATATAT others(7): Show |
A | 2 | a0002c0005t0006g0249a0002c0005t0007g0012 | 2 | HG02486.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.89-2522_89-2509del others(14): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864295 | |||||
| chr22:41864307
|
A | G | 1 | a0002c0002t0002g0090 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.89-2524A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864307 | ||||||
| chr22:41864309
|
G | A | 1 | a0002c0002t0002g0090 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.89-2522G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864309 | ||||||
| chr22:41864309
|
G | GTA | 4 | a0001c0020t0001g0286a0002c0002t0003g0329a0002c0002t0009g0320others(1): Show | 4 | HG00099.hp2 HG01109.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-2508_89-2507dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864309 | |||||
| chr22:41864309
|
G | GTATA | 4 | a0002c0002t0001g0029a0004c0004t0003g0004a0004c0004t0011g0043others(1): Show | 4 | HG00423.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-2510_89-2507dup others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864309 | |||||
| chr22:41864322
|
TA | T | 40 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(37): Show | 41 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-2508delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864322 | ||||||
| chr22:41864323
|
A | ATAT | 6 | a0002c0002t0003g0008a0002c0002t0003g0055a0002c0002t0003g0056others(3): Show | 6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-2507_89-2506ins others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864323 | |||||
| chr22:41864323
|
A | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(41): Show | 45 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.89-2508A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864323 | ||||||
| chr22:41864323
|
AT | A | 9 | a0002c0002t0001g0136a0002c0002t0001g0142a0002c0002t0001g0143others(6): Show | 9 | HG00280.hp2 HG00621.hp2 HG04115.hp2 others(6): Show |
intron_variant | MODIFIER | c.89-2493delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41864323 | |||||
| chr22:41864324
|
T | TA | 65 | a0001c0001t0001g0218a0001c0001t0008g0112a0001c0001t0008g0243others(62): Show | 66 | HG00597.hp2 HG00621.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.89-2507_89-2506ins others(1): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864324 | ||||||
| chr22:41864324
|
T | TATA | 24 | a0002c0002t0001g0030a0002c0002t0001g0031a0002c0002t0001g0032others(21): Show | 24 | HG00408.hp2 HG00673.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.89-2507_89-2506ins others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864324 | ||||||
| chr22:41864324
|
T | TATATA | 3 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040 | 3 | HG01934.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.89-2507_89-2506ins others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864324 | ||||||
| chr22:41864325
|
T | A | 40 | a0001c0001t0001g0230a0001c0001t0001g0232a0001c0001t0001g0236others(37): Show | 40 | HG00140.hp1 HG00423.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.89-2506T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864325 | ||||||
| chr22:41864326
|
T | A | 82 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(79): Show | 83 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.89-2505T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864326 | ||||||
| chr22:41864327
|
T | A | 6 | a0002c0002t0001g0029a0002c0002t0003g0329a0003c0010t0022g0022others(3): Show | 6 | HG00423.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2504T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864327 | ||||||
| chr22:41864328
|
T | A | 1 | a0002c0002t0002g0062 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.89-2503T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864328 | ||||||
| chr22:41864329
|
T | A | 1 | a0002c0002t0001g0029 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.89-2502T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864329 | ||||||
| chr22:41864333
|
T | C | 1 | a0008c0014t0006g0023 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.89-2498T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864333 | ||||||
| chr22:41864609
|
C | T | 1 | a0004c0004t0010g0044 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.89-2222C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864609 | ||||||
| chr22:41864646
|
G | C | 1 | a0002c0002t0013g0054 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.89-2185G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864646 | ||||||
| chr22:41864967
|
C | G | 59 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(56): Show | 60 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-1864C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41864967 | ||||||
| chr22:41865146
|
A | C | 1 | a0001c0001t0001g0307 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.89-1685A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41865146 | ||||||
| chr22:41865146
|
AAC | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(98): Show | 102 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.89-1663_89-1662del others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41865146 | |||||
| chr22:41865146
|
AACAC | A | 149 | a0002c0002t0001g0002a0002c0002t0001g0029a0002c0002t0001g0030others(146): Show | 151 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.89-1665_89-1662del others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr22 | 41865146 | |||||
| chr22:41865327
|
T | A | 1 | a0001c0001t0001g0280 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.89-1504T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41865327 | ||||||
| chr22:41865356
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0216a0001c0001t0012g0213 | 3 | HG01517.hp1 HG01943.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.89-1475C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41865356 | ||||||
| chr22:41865968
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.89-863C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41865968 | ||||||
| chr22:41866037
|
C | T | 1 | a0004c0004t0011g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.89-794C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866037 | ||||||
| chr22:41866043
|
G | A | 1 | a0003c0003t0004g0137 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.89-788G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866043 | ||||||
| chr22:41866116
|
C | T | 3 | a0002c0002t0003g0328a0002c0002t0003g0333a0002c0002t0006g0006 | 3 | HG01884.hp1 HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.89-715C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866116 | ||||||
| chr22:41866209
|
G | A | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.89-622G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866209 | ||||||
| chr22:41866325
|
T | C | 12 | a0002c0002t0002g0047a0002c0002t0002g0108a0004c0004t0001g0042others(9): Show | 12 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-506T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866325 | ||||||
| chr22:41866407
|
G | A | 4 | a0002c0002t0002g0117a0002c0002t0002g0147a0002c0002t0002g0148others(1): Show | 4 | HG00642.hp2 HG03831.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-424G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866407 | ||||||
| chr22:41866427
|
A | G | 332 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(329): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.89-404A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866427 | ||||||
| chr22:41866443
|
A | G | 250 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(247): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.89-388A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 1/18 | chr22 | 41866443 | ||||||
| chr22:41867663
|
C | T | 1 | a0002c0002t0005g0019 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.538+383C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41867663 | ||||||
| chr22:41867680
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.538+400G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41867680 | ||||||
| chr22:41867694
|
C | A | 1 | a0002c0002t0002g0074 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.538+414C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41867694 | ||||||
| chr22:41867813
|
G | GA | 38 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(35): Show | 38 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.538+544dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr22 | 41867813 | |||||
| chr22:41868265
|
G | T | 167 | a0002c0002t0001g0002a0002c0002t0001g0029a0002c0002t0001g0030others(164): Show | 169 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.539-346G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41868265 | ||||||
| chr22:41868307
|
G | A | 1 | a0002c0002t0003g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.539-304G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 2/18 | chr22 | 41868307 | ||||||
| chr22:41869186
|
C | T | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.720+394C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869186 | ||||||
| chr22:41869296
|
G | GGTTTTAC others(1): Show |
162 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0175others(159): Show | 164 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.720+504_720+505ins others(8): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869296 | ||||||
| chr22:41869300
|
T | C | 6 | a0002c0002t0003g0008a0002c0002t0003g0055a0002c0002t0003g0056others(3): Show | 6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+508T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869300 | ||||||
| chr22:41869327
|
C | T | 1 | a0003c0003t0004g0116 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.720+535C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869327 | ||||||
| chr22:41869338
|
C | T | 1 | a0002c0002t0005g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.720+546C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869338 | ||||||
| chr22:41869373
|
C | T | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.720+581C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869373 | ||||||
| chr22:41869426
|
G | A | 51 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(48): Show | 52 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.720+634G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869426 | ||||||
| chr22:41869464
|
G | T | 1 | a0001c0001t0001g0303 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.720+672G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869464 | ||||||
| chr22:41869489
|
A | AT | 10 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0166others(7): Show | 11 | HG00544.hp2 HG00597.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.720+709dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41869489 | |||||
| chr22:41869501
|
TG | T | 167 | a0001c0001t0001g0189a0002c0002t0001g0002a0002c0002t0001g0029others(164): Show | 169 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.720+711delG | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41869501 | |||||
| chr22:41869502
|
G | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(78): Show | 82 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.720+710G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869502 | ||||||
| chr22:41869529
|
G | C | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.720+737G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869529 | ||||||
| chr22:41869596
|
G | A | 4 | a0002c0005t0007g0012a0002c0005t0007g0248a0002c0005t0007g0250others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+804G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869596 | ||||||
| chr22:41869597
|
C | A | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.720+805C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869597 | ||||||
| chr22:41869609
|
A | G | 1 | a0003c0017t0004g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.720+817A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869609 | ||||||
| chr22:41869677
|
G | A | 3 | a0006c0008t0003g0113a0006c0008t0003g0114a0006c0008t0003g0115 | 3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.720+885G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869677 | ||||||
| chr22:41869862
|
CT | C | 31 | a0001c0001t0001g0202a0002c0002t0001g0029a0002c0002t0001g0030others(28): Show | 31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.721-1014delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41869862 | |||||
| chr22:41869916
|
C | T | 19 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(16): Show | 19 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.721-973C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41869916 | ||||||
| chr22:41870164
|
T | G | 54 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(51): Show | 55 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.721-725T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41870164 | ||||||
| chr22:41870415
|
A | G | 250 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(247): Show | 253 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.721-474A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | chr22 | 41870415 | ||||||
| chr22:41870628
|
C | CA | 34 | a0001c0001t0001g0190a0001c0001t0001g0202a0001c0001t0001g0242others(31): Show | 34 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.721-238dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41870628 | |||||
| chr22:41870628
|
C | CAA | 10 | a0002c0002t0001g0031a0002c0002t0001g0032a0002c0002t0001g0034others(7): Show | 10 | HG01934.hp1 HG02004.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.721-239_721-238dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41870628 | |||||
| chr22:41870628
|
CA | C | 171 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(168): Show | 174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.721-238delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr22 | 41870628 | |||||
| chr22:41871192
|
C | T | 30 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(27): Show | 30 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.867+157C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871192 | ||||||
| chr22:41871347
|
C | G | 1 | a0002c0002t0005g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.867+312C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871347 | ||||||
| chr22:41871601
|
C | A | 248 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(245): Show | 251 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.867+566C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871601 | ||||||
| chr22:41871619
|
C | T | 31 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.867+584C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871619 | ||||||
| chr22:41871700
|
T | A | 1 | a0002c0002t0002g0104 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.867+665T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871700 | ||||||
| chr22:41871788
|
A | C | 1 | a0002c0002t0002g0062 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.867+753A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871788 | ||||||
| chr22:41871796
|
G | A | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.867+761G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871796 | ||||||
| chr22:41871898
|
C | CA | 90 | a0001c0001t0001g0202a0001c0001t0001g0266a0001c0001t0001g0278others(87): Show | 91 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.867+879dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 41871898 | |||||
| chr22:41871898
|
C | CAA | 62 | a0002c0002t0001g0034a0002c0002t0001g0106a0002c0002t0001g0107others(59): Show | 63 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.867+878_867+879dup others(2): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 41871898 | |||||
| chr22:41871976
|
C | T | 13 | a0002c0002t0001g0118a0002c0002t0001g0120a0002c0002t0001g0121others(10): Show | 13 | NA18951.hp2 NA18965.hp2 NA18967.hp2 others(10): Show |
intron_variant | MODIFIER | c.867+941C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41871976 | ||||||
| chr22:41872024
|
G | A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.867+989G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872024 | ||||||
| chr22:41872106
|
C | T | 18 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.867+1071C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872106 | ||||||
| chr22:41872225
|
G | A | 1 | a0002c0005t0006g0249 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.867+1190G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872225 | ||||||
| chr22:41872245
|
G | A | 31 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.867+1210G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872245 | ||||||
| chr22:41872249
|
CA | C | 148 | a0001c0001t0001g0228a0002c0002t0001g0002a0002c0002t0001g0029others(145): Show | 150 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.867+1229delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 41872249 | |||||
| chr22:41872677
|
G | A | 2 | a0002c0002t0001g0106a0002c0002t0001g0107 | 2 | HG00597.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.868-1121G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872677 | ||||||
| chr22:41872717
|
C | T | 60 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.868-1081C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41872717 | ||||||
| chr22:41872892
|
C | CA | 8 | a0001c0001t0001g0193a0001c0001t0003g0210a0002c0002t0003g0008others(5): Show | 8 | HG00558.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.868-895dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr22 | 41872892 | |||||
| chr22:41873124
|
G | A | 31 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.868-674G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873124 | ||||||
| chr22:41873184
|
C | T | 1 | a0002c0002t0002g0062 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.868-614C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873184 | ||||||
| chr22:41873370
|
T | G | 8 | a0002c0002t0002g0047a0002c0002t0002g0067a0002c0002t0002g0078others(5): Show | 8 | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.868-428T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873370 | ||||||
| chr22:41873449
|
G | A | 1 | a0002c0002t0002g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.868-349G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873449 | ||||||
| chr22:41873467
|
C | G | 1 | a0001c0001t0019g0195 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.868-331C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873467 | ||||||
| chr22:41873525
|
A | G | 1 | a0001c0001t0019g0195 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.868-273A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873525 | ||||||
| chr22:41873528
|
C | T | 11 | a0001c0001t0001g0231a0001c0001t0001g0238a0001c0001t0001g0239others(8): Show | 11 | HG00280.hp1 HG00639.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.868-270C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873528 | ||||||
| chr22:41873559
|
T | C | 2 | a0002c0002t0006g0006a0002c0002t0006g0048 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.868-239T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873559 | ||||||
| chr22:41873624
|
C | T | 75 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(72): Show | 76 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.868-174C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873624 | ||||||
| chr22:41873721
|
C | T | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.868-77C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873721 | ||||||
| chr22:41873727
|
G | T | 3 | a0004c0004t0003g0004a0004c0004t0011g0043a0004c0004t0011g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.868-71G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873727 | ||||||
| chr22:41873763
|
G | A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.868-35G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 4/18 | chr22 | 41873763 | ||||||
| chr22:41874084
|
G | T | 1 | a0004c0004t0001g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1089+65G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874084 | ||||||
| chr22:41874230
|
G | C | 2 | a0002c0002t0002g0047a0002c0002t0002g0108 | 2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1089+211G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874230 | ||||||
| chr22:41874319
|
C | G | 1 | a0001c0001t0001g0326 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1089+300C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874319 | ||||||
| chr22:41874645
|
C | T | 6 | a0002c0002t0003g0008a0002c0002t0003g0055a0002c0002t0003g0056others(3): Show | 6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089+626C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874645 | ||||||
| chr22:41874703
|
C | A | 60 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1090-634C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874703 | ||||||
| chr22:41874813
|
A | C | 2 | a0002c0002t0002g0092a0009c0019t0001g0093 | 2 | HG03942.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1090-524A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874813 | ||||||
| chr22:41874840
|
G | A | 57 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(54): Show | 58 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1090-497G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874840 | ||||||
| chr22:41874860
|
T | C | 12 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(9): Show | 12 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.1090-477T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874860 | ||||||
| chr22:41874870
|
G | C | 2 | a0002c0002t0002g0092a0009c0019t0001g0093 | 2 | HG03942.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1090-467G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874870 | ||||||
| chr22:41874931
|
A | G | 1 | a0002c0002t0002g0101 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1090-406A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41874931 | ||||||
| chr22:41875026
|
A | C | 3 | a0004c0004t0003g0004a0004c0004t0011g0043a0004c0004t0011g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1090-311A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875026 | ||||||
| chr22:41875050
|
G | A | 5 | a0001c0001t0001g0255a0001c0001t0001g0287a0001c0001t0001g0301others(2): Show | 5 | NA18973.hp1 NA18988.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-287G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875050 | ||||||
| chr22:41875117
|
C | A | 1 | a0002c0002t0005g0021 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1090-220C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875117 | ||||||
| chr22:41875263
|
G | A | 1 | a0001c0012t0001g0312 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1090-74G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875263 | ||||||
| chr22:41875289
|
T | C | 7 | a0002c0002t0002g0047a0002c0002t0002g0078a0002c0002t0002g0079others(4): Show | 7 | HG02572.hp2 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1090-48T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 5/18 | chr22 | 41875289 | ||||||
| chr22:41875756
|
A | G | 2 | a0004c0004t0001g0042a0004c0004t0001g0050 | 2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1386+32A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41875756 | ||||||
| chr22:41875838
|
A | G | 2 | a0004c0004t0011g0043a0004c0004t0011g0051 | 2 | HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1386+114A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41875838 | ||||||
| chr22:41875951
|
G | A | 3 | a0004c0004t0003g0004a0004c0004t0011g0043a0004c0004t0011g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1386+227G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41875951 | ||||||
| chr22:41876031
|
C | A | 2 | a0002c0002t0003g0052a0002c0002t0003g0053 | 2 | HG02886.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1386+307C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876031 | ||||||
| chr22:41876211
|
A | T | 8 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1386+487A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876211 | ||||||
| chr22:41876266
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1386+542G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876266 | ||||||
| chr22:41876342
|
G | A | 2 | a0002c0009t0002g0208a0002c0009t0002g0226 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1386+618G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876342 | ||||||
| chr22:41876389
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1386+665G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876389 | ||||||
| chr22:41876538
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1387-691A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876538 | ||||||
| chr22:41876588
|
A | C | 1 | a0002c0002t0005g0016 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1387-641A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876588 | ||||||
| chr22:41876829
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1387-400C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41876829 | ||||||
| chr22:41877089
|
G | C | 1 | a0002c0002t0002g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1387-140G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 7/18 | chr22 | 41877089 | ||||||
| chr22:41877458
|
G | A | 31 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(28): Show | 31 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.1579+37G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877458 | ||||||
| chr22:41877510
|
C | T | 1 | a0002c0002t0001g0040 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1579+89C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877510 | ||||||
| chr22:41877724
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1580-218A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877724 | ||||||
| chr22:41877838
|
A | G | 18 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(15): Show | 18 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1580-104A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877838 | ||||||
| chr22:41877929
|
C | T | 3 | a0002c0002t0003g0065a0002c0002t0003g0076a0002c0002t0003g0109 | 3 | HG01243.hp2 HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1580-13C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 8/18 | chr22 | 41877929 | ||||||
| chr22:41878283
|
G | A | 60 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(57): Show | 61 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1761+160G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41878283 | ||||||
| chr22:41878398
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1761+275G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41878398 | ||||||
| chr22:41878553
|
G | A | 1 | a0002c0002t0008g0332 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1761+430G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41878553 | ||||||
| chr22:41878877
|
G | A | 1 | a0002c0002t0002g0110 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1761+754G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41878877 | ||||||
| chr22:41879081
|
G | T | 1 | a0002c0002t0006g0048 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1761+958G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879081 | ||||||
| chr22:41879411
|
A | G | 32 | a0002c0002t0001g0029a0002c0002t0001g0030a0002c0002t0001g0031others(29): Show | 32 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1761+1288A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879411 | ||||||
| chr22:41879472
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1762-1244G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879472 | ||||||
| chr22:41879504
|
G | C | 2 | a0002c0005t0006g0013a0002c0005t0006g0249 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1762-1212G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879504 | ||||||
| chr22:41879566
|
G | A | 2 | a0002c0002t0003g0076a0002c0002t0003g0109 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1762-1150G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879566 | ||||||
| chr22:41879705
|
C | T | 3 | a0002c0002t0003g0065a0002c0002t0003g0076a0002c0002t0003g0109 | 3 | HG01243.hp2 HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1762-1011C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879705 | ||||||
| chr22:41879975
|
A | T | 4 | a0002c0005t0007g0012a0002c0005t0007g0248a0002c0005t0007g0250others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1762-741A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41879975 | ||||||
| chr22:41880274
|
G | A | 1 | a0001c0001t0003g0010 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1762-442G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880274 | ||||||
| chr22:41880284
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0012g0213 | 2 | HG01943.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1762-432G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880284 | ||||||
| chr22:41880287
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0012g0213 | 2 | HG01943.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1762-429C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880287 | ||||||
| chr22:41880383
|
C | G | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1762-333C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880383 | ||||||
| chr22:41880397
|
C | CA | 102 | a0001c0001t0001g0094a0001c0001t0001g0188a0001c0001t0001g0190others(99): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1762-300dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr22 | 41880397 | |||||
| chr22:41880397
|
C | CAA | 6 | a0001c0001t0003g0210a0002c0002t0002g0110a0002c0002t0009g0320others(3): Show | 6 | HG01109.hp2 HG01175.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1762-301_1762-300d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr22 | 41880397 | |||||
| chr22:41880452
|
C | T | 3 | a0004c0004t0010g0044a0004c0004t0010g0045a0004c0004t0010g0046 | 3 | HG02559.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1762-264C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880452 | ||||||
| chr22:41880578
|
G | C | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1762-138G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 9/18 | chr22 | 41880578 | ||||||
| chr22:41881115
|
G | A | 1 | a0002c0002t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2038+123G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881115 | ||||||
| chr22:41881713
|
G | T | 1 | a0002c0016t0002g0083 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2038+721G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881713 | ||||||
| chr22:41881788
|
C | A | 47 | a0002c0002t0001g0106a0002c0002t0001g0107a0002c0002t0002g0001others(44): Show | 48 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.2038+796C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881788 | ||||||
| chr22:41881882
|
G | A | 1 | a0002c0005t0016g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2038+890G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881882 | ||||||
| chr22:41881901
|
A | G | 1 | a0001c0011t0001g0262 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2038+909A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41881901 | ||||||
| chr22:41882215
|
T | C | 1 | a0002c0002t0001g0129 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2038+1223T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882215 | ||||||
| chr22:41882241
|
A | G | 32 | a0001c0001t0001g0201a0002c0002t0001g0029a0002c0002t0001g0030others(29): Show | 32 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.2038+1249A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882241 | ||||||
| chr22:41882320
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2038+1328G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882320 | ||||||
| chr22:41882562
|
T | C | 63 | a0001c0001t0001g0175a0002c0002t0001g0002a0002c0002t0001g0118others(60): Show | 64 | HG00099.hp1 HG00621.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.2038+1570T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882562 | ||||||
| chr22:41882571
|
C | G | 1 | a0008c0014t0006g0023 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2038+1579C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882571 | ||||||
| chr22:41882953
|
A | G | 8 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2039-1889A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41882953 | ||||||
| chr22:41883054
|
C | T | 1 | a0002c0002t0003g0329 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2039-1788C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883054 | ||||||
| chr22:41883331
|
C | T | 2 | a0002c0002t0003g0328a0002c0002t0003g0333 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2039-1511C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883331 | ||||||
| chr22:41883397
|
G | A | 16 | a0002c0002t0002g0047a0002c0002t0002g0078a0002c0002t0002g0079others(13): Show | 16 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.2039-1445G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883397 | ||||||
| chr22:41883502
|
G | C | 75 | a0001c0001t0001g0281a0001c0001t0003g0306a0001c0001t0003g0309others(72): Show | 76 | HG00140.hp2 HG00280.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.2039-1340G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883502 | ||||||
| chr22:41883567
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2039-1275C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883567 | ||||||
| chr22:41883649
|
A | G | 44 | a0001c0001t0001g0094a0001c0001t0001g0209a0001c0001t0001g0214others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.2039-1193A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883649 | ||||||
| chr22:41883886
|
G | A | 1 | a0001c0001t0014g0221 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2039-956G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41883886 | ||||||
| chr22:41884010
|
G | C | 3 | a0002c0002t0001g0129a0003c0003t0004g0122a0003c0003t0004g0123 | 3 | NA18939.hp1 NA18969.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2039-832G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884010 | ||||||
| chr22:41884060
|
T | TG | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(147): Show | 152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.2039-781dupG | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr22 | 41884060 | |||||
| chr22:41884130
|
C | CA | 9 | a0001c0001t0001g0188a0002c0002t0005g0014a0002c0002t0005g0015others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2039-712_2039-711i others(3): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884130 | ||||||
| chr22:41884131
|
G | A | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(118): Show | 123 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.2039-711G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884131 | ||||||
| chr22:41884133
|
G | T | 9 | a0001c0001t0001g0188a0002c0002t0005g0014a0002c0002t0005g0015others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2039-709G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884133 | ||||||
| chr22:41884134
|
T | G | 1 | a0002c0002t0002g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2039-708T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884134 | ||||||
| chr22:41884226
|
C | T | 1 | a0002c0002t0005g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2039-616C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884226 | ||||||
| chr22:41884357
|
G | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(188): Show | 193 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.2039-485G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884357 | ||||||
| chr22:41884383
|
G | A | 1 | a0002c0015t0002g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2039-459G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884383 | ||||||
| chr22:41884614
|
T | C | 113 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0002others(110): Show | 114 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.2039-228T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884614 | ||||||
| chr22:41884769
|
G | A | 1 | a0007c0026t0001g0308 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2039-73G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 10/18 | chr22 | 41884769 | ||||||
| chr22:41885145
|
T | G | 35 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0029others(32): Show | 35 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.2208+134T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885145 | ||||||
| chr22:41885151
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2208+140G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885151 | ||||||
| chr22:41885251
|
C | A | 34 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0029others(31): Show | 34 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2208+240C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885251 | ||||||
| chr22:41885256
|
G | T | 1 | a0002c0002t0002g0081 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2208+245G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885256 | ||||||
| chr22:41885290
|
A | G | 34 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0029others(31): Show | 34 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2208+279A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885290 | ||||||
| chr22:41885425
|
A | G | 258 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(255): Show | 261 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.2208+414A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885425 | ||||||
| chr22:41885557
|
C | T | 4 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0322others(1): Show | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2208+546C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885557 | ||||||
| chr22:41885583
|
C | T | 34 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0029others(31): Show | 34 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.2208+572C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41885583 | ||||||
| chr22:41886008
|
C | T | 62 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(59): Show | 63 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.2208+997C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886008 | ||||||
| chr22:41886254
|
A | G | 1 | a0001c0001t0004g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2208+1243A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886254 | ||||||
| chr22:41886263
|
C | G | 3 | a0001c0001t0003g0306a0001c0001t0003g0309a0001c0001t0003g0310 | 3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2208+1252C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886263 | ||||||
| chr22:41886755
|
C | T | 8 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2208+1744C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886755 | ||||||
| chr22:41886812
|
T | A | 1 | a0001c0001t0014g0221 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2208+1801T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41886812 | ||||||
| chr22:41886939
|
C | CA | 4 | a0002c0002t0002g0062a0002c0002t0003g0024a0002c0002t0003g0026others(1): Show | 4 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.2208+1929dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41886939 | |||||
| chr22:41887010
|
G | A | 1 | a0002c0002t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2208+1999G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887010 | ||||||
| chr22:41887071
|
T | C | 116 | a0001c0001t0001g0265a0001c0001t0001g0275a0001c0001t0004g0245others(113): Show | 117 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.2208+2060T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887071 | ||||||
| chr22:41887142
|
G | A | 3 | a0001c0001t0003g0306a0001c0001t0003g0309a0001c0001t0003g0310 | 3 | HG01433.hp1 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2208+2131G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887142 | ||||||
| chr22:41887397
|
C | T | 10 | a0004c0004t0001g0042a0004c0004t0001g0050a0004c0004t0001g0227others(7): Show | 10 | HG02257.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.2208+2386C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887397 | ||||||
| chr22:41887405
|
C | T | 2 | a0003c0003t0004g0122a0003c0003t0004g0123 | 2 | NA18939.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.2208+2394C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887405 | ||||||
| chr22:41887533
|
G | A | 1 | a0009c0019t0001g0093 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2208+2522G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887533 | ||||||
| chr22:41887546
|
T | G | 55 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(52): Show | 56 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.2208+2535T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887546 | ||||||
| chr22:41887547
|
A | T | 55 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(52): Show | 56 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.2208+2536A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887547 | ||||||
| chr22:41887705
|
G | A | 38 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0029others(35): Show | 38 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.2208+2694G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887705 | ||||||
| chr22:41887769
|
C | T | 2 | a0002c0009t0002g0208a0002c0009t0002g0226 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2208+2758C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41887769 | ||||||
| chr22:41887838
|
A | AT | 8 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2208+2834dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41887838 | |||||
| chr22:41887838
|
AT | A | 6 | a0002c0005t0007g0012a0002c0005t0007g0246a0002c0005t0007g0247others(3): Show | 6 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2208+2834delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41887838 | |||||
| chr22:41888256
|
C | T | 61 | a0001c0001t0002g0257a0001c0001t0003g0306a0001c0001t0003g0309others(58): Show | 62 | HG00280.hp2 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.2208+3245C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41888256 | ||||||
| chr22:41888469
|
T | TCTG | 114 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0002others(111): Show | 115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.2208+3460_2208+346 others(7): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41888469 | |||||
| chr22:41888862
|
CT | C | 3 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0200 | 3 | NA18947.hp2 NA18977.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2208+3852delT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41888862 | ||||||
| chr22:41888969
|
T | G | 1 | a0004c0004t0006g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2208+3958T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41888969 | ||||||
| chr22:41889059
|
A | T | 114 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0002others(111): Show | 115 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.2208+4048A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889059 | ||||||
| chr22:41889073
|
A | G | 1 | a0002c0002t0001g0120 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2209-4044A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889073 | ||||||
| chr22:41889097
|
A | G | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-4020A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889097 | ||||||
| chr22:41889216
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2209-3901C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889216 | ||||||
| chr22:41889262
|
G | A | 10 | a0002c0002t0003g0052a0002c0002t0003g0053a0002c0002t0005g0014others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2209-3855G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889262 | ||||||
| chr22:41889338
|
G | T | 8 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2209-3779G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889338 | ||||||
| chr22:41889376
|
C | T | 2 | a0001c0001t0012g0178a0001c0001t0020g0179 | 2 | HG02155.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2209-3741C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889376 | ||||||
| chr22:41889486
|
G | A | 1 | a0001c0001t0004g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2209-3631G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889486 | ||||||
| chr22:41889684
|
T | G | 9 | a0002c0005t0006g0013a0002c0005t0006g0249a0002c0005t0007g0012others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.2209-3433T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889684 | ||||||
| chr22:41889701
|
TA | T | 237 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(234): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2209-3401delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41889701 | |||||
| chr22:41889715
|
AAG | A | 76 | a0002c0002t0001g0002a0002c0002t0001g0118a0002c0002t0001g0120others(73): Show | 77 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.2209-3399_2209-339 others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41889715 | |||||
| chr22:41889728
|
C | T | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2209-3389C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889728 | ||||||
| chr22:41889810
|
G | C | 8 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2209-3307G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889810 | ||||||
| chr22:41889830
|
G | A | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-3287G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889830 | ||||||
| chr22:41889864
|
C | G | 116 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0002others(113): Show | 117 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.2209-3253C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889864 | ||||||
| chr22:41889940
|
G | A | 1 | a0004c0004t0006g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2209-3177G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41889940 | ||||||
| chr22:41890003
|
AAG | A | 10 | a0002c0005t0006g0013a0002c0005t0006g0249a0002c0005t0007g0012others(7): Show | 10 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2209-3106_2209-310 others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41890003 | |||||
| chr22:41890026
|
T | G | 1 | a0001c0001t0001g0288 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2209-3091T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890026 | ||||||
| chr22:41890092
|
T | A | 1 | a0008c0014t0006g0023 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2209-3025T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890092 | ||||||
| chr22:41890176
|
T | C | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-2941T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890176 | ||||||
| chr22:41890195
|
A | C | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-2922A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890195 | ||||||
| chr22:41890251
|
G | A | 38 | a0001c0001t0001g0265a0001c0001t0001g0275a0002c0002t0001g0029others(35): Show | 38 | HG00408.hp2 HG00423.hp2 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.2209-2866G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890251 | ||||||
| chr22:41890287
|
C | T | 7 | a0002c0002t0002g0047a0002c0002t0002g0078a0002c0002t0002g0079others(4): Show | 7 | HG02572.hp2 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2209-2830C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890287 | ||||||
| chr22:41890445
|
G | A | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2209-2672G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890445 | ||||||
| chr22:41890672
|
A | AT | 78 | a0001c0001t0001g0222a0001c0001t0002g0327a0001c0001t0003g0010others(75): Show | 79 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.2209-2432dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41890672 | |||||
| chr22:41890672
|
A | ATT | 14 | a0001c0001t0001g0218a0002c0002t0001g0136a0002c0002t0003g0109others(11): Show | 14 | HG01099.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.2209-2433_2209-243 others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41890672 | |||||
| chr22:41890773
|
T | C | 1 | a0003c0017t0004g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2209-2344T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890773 | ||||||
| chr22:41890882
|
T | C | 1 | a0002c0002t0003g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2209-2235T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41890882 | ||||||
| chr22:41891144
|
C | T | 3 | a0004c0004t0010g0044a0004c0004t0010g0045a0004c0004t0010g0046 | 3 | HG02559.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2209-1973C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891144 | ||||||
| chr22:41891186
|
C | T | 8 | a0001c0001t0001g0218a0001c0001t0001g0222a0001c0001t0003g0010others(5): Show | 8 | HG01099.hp2 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.2209-1931C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891186 | ||||||
| chr22:41891199
|
C | G | 3 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0217 | 3 | HG00733.hp1 HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2209-1918C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891199 | ||||||
| chr22:41891301
|
G | A | 1 | a0002c0002t0002g0081 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2209-1816G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891301 | ||||||
| chr22:41891364
|
G | A | 2 | a0003c0003t0004g0122a0003c0003t0004g0123 | 2 | NA18939.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.2209-1753G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891364 | ||||||
| chr22:41891450
|
A | G | 246 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0070others(243): Show | 248 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.2209-1667A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891450 | ||||||
| chr22:41891765
|
T | A | 1 | a0002c0005t0016g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2209-1352T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891765 | ||||||
| chr22:41891789
|
T | C | 1 | a0002c0002t0001g0144 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2209-1328T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891789 | ||||||
| chr22:41891838
|
T | C | 2 | a0002c0005t0006g0013a0002c0005t0006g0249 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2209-1279T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891838 | ||||||
| chr22:41891851
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0182others(2): Show | 6 | NA18747.hp1 NA18948.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.2209-1266A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891851 | ||||||
| chr22:41891902
|
C | T | 4 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0322others(1): Show | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2209-1215C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891902 | ||||||
| chr22:41891962
|
C | T | 25 | a0001c0001t0001g0285a0001c0001t0001g0299a0003c0003t0004g0097others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.2209-1155C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41891962 | ||||||
| chr22:41892051
|
C | G | 2 | a0001c0001t0013g0220a0002c0002t0013g0054 | 2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2209-1066C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892051 | ||||||
| chr22:41892068
|
A | G | 2 | a0003c0003t0004g0125a0003c0003t0004g0134 | 2 | HG00099.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2209-1049A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892068 | ||||||
| chr22:41892126
|
G | C | 4 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0322others(1): Show | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2209-991G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892126 | ||||||
| chr22:41892137
|
G | C | 1 | a0003c0017t0004g0041 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2209-980G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892137 | ||||||
| chr22:41892256
|
C | T | 6 | a0002c0002t0003g0008a0002c0002t0003g0055a0002c0002t0003g0056others(3): Show | 6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2209-861C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892256 | ||||||
| chr22:41892365
|
A | C | 1 | a0001c0001t0001g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2209-752A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892365 | ||||||
| chr22:41892477
|
G | A | 1 | a0001c0001t0003g0224 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2209-640G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892477 | ||||||
| chr22:41892541
|
G | A | 40 | a0001c0001t0004g0245a0001c0001t0005g0018a0001c0001t0014g0221others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.2209-576G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892541 | ||||||
| chr22:41892562
|
G | A | 5 | a0001c0001t0001g0254a0001c0001t0001g0282a0001c0001t0001g0304others(2): Show | 5 | NA18946.hp1 NA18962.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.2209-555G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892562 | ||||||
| chr22:41892647
|
C | CA | 151 | a0001c0001t0001g0171a0001c0001t0001g0180a0001c0001t0001g0181others(148): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2209-449dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41892647 | |||||
| chr22:41892647
|
C | CAA | 15 | a0001c0001t0001g0184a0001c0001t0001g0222a0002c0002t0001g0031others(12): Show | 15 | HG01192.hp1 HG01261.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2209-450_2209-449d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41892647 | |||||
| chr22:41892647
|
C | CAAA | 6 | a0001c0001t0013g0220a0002c0002t0013g0054a0002c0005t0016g0251others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2209-451_2209-449d others(5): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41892647 | |||||
| chr22:41892647
|
CA | C | 16 | a0001c0001t0001g0169a0001c0001t0001g0174a0001c0001t0001g0259others(13): Show | 16 | HG01261.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.2209-449delA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr22 | 41892647 | |||||
| chr22:41892745
|
C | A | 12 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2209-372C>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892745 | ||||||
| chr22:41892990
|
T | G | 57 | a0001c0001t0004g0245a0001c0001t0005g0018a0001c0001t0008g0112others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2209-127T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41892990 | ||||||
| chr22:41893092
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2209-25A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 11/18 | chr22 | 41893092 | ||||||
| chr22:41893295
|
C | G | 2 | a0002c0005t0006g0013a0002c0005t0006g0249 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2377+10C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893295 | ||||||
| chr22:41893313
|
T | C | 12 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2377+28T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893313 | ||||||
| chr22:41893366
|
C | T | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2377+81C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893366 | ||||||
| chr22:41893401
|
C | CGTTT | 28 | a0001c0001t0001g0201a0001c0001t0012g0213a0001c0011t0001g0289others(25): Show | 28 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.2377+142_2377+145d others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr22 | 41893401 | |||||
| chr22:41893418
|
G | T | 1 | a0001c0007t0003g0007 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2377+133G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893418 | ||||||
| chr22:41893462
|
T | C | 57 | a0001c0001t0004g0245a0001c0001t0005g0018a0001c0001t0008g0112others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2377+177T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893462 | ||||||
| chr22:41893496
|
G | A | 53 | a0001c0001t0002g0257a0001c0001t0002g0327a0001c0001t0015g0319others(50): Show | 54 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.2377+211G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893496 | ||||||
| chr22:41893561
|
C | T | 14 | a0001c0001t0005g0018a0001c0001t0014g0221a0002c0002t0005g0014others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2377+276C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893561 | ||||||
| chr22:41893793
|
C | T | 25 | a0002c0018t0004g0159a0003c0003t0004g0097a0003c0003t0004g0105others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2377+508C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893793 | ||||||
| chr22:41893800
|
A | G | 14 | a0001c0001t0005g0018a0001c0001t0014g0221a0002c0002t0005g0014others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2377+515A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893800 | ||||||
| chr22:41893969
|
T | C | 1 | a0003c0003t0004g0116 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2377+684T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41893969 | ||||||
| chr22:41894030
|
C | T | 2 | a0001c0001t0013g0220a0002c0002t0013g0054 | 2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2377+745C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894030 | ||||||
| chr22:41894173
|
T | C | 57 | a0001c0001t0004g0245a0001c0001t0005g0018a0001c0001t0008g0112others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2378-647T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894173 | ||||||
| chr22:41894222
|
C | T | 1 | a0004c0004t0011g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2378-598C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894222 | ||||||
| chr22:41894317
|
G | A | 1 | a0002c0005t0007g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2378-503G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894317 | ||||||
| chr22:41894486
|
C | T | 3 | a0002c0002t0003g0024a0002c0002t0003g0026a0002c0002t0003g0066 | 3 | HG00738.hp1 HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2378-334C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894486 | ||||||
| chr22:41894502
|
T | C | 1 | a0003c0003t0004g0125 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2378-318T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894502 | ||||||
| chr22:41894674
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2378-146T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 12/18 | chr22 | 41894674 | ||||||
| chr22:41895014
|
C | T | 1 | a0002c0002t0001g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2495+77C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895014 | ||||||
| chr22:41895118
|
C | G | 12 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2495+181C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895118 | ||||||
| chr22:41895140
|
G | GT | 42 | a0001c0001t0001g0177a0001c0001t0001g0185a0001c0001t0001g0199others(39): Show | 42 | HG00544.hp2 HG00597.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.2495+219dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 41895140 | |||||
| chr22:41895170
|
C | T | 1 | a0001c0001t0001g0301 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2495+233C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895170 | ||||||
| chr22:41895240
|
C | T | 12 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2495+303C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895240 | ||||||
| chr22:41895330
|
G | A | 1 | a0002c0002t0006g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2495+393G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895330 | ||||||
| chr22:41895403
|
T | C | 1 | a0002c0013t0001g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2495+466T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895403 | ||||||
| chr22:41895431
|
C | CT | 29 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0187others(26): Show | 29 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.2495+515dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 41895431 | |||||
| chr22:41895431
|
C | CTT | 9 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495+514_2495+515d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 41895431 | |||||
| chr22:41895453
|
G | C | 5 | a0001c0007t0003g0007a0001c0007t0003g0086a0001c0007t0003g0087others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495+516G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895453 | ||||||
| chr22:41895466
|
G | A | 5 | a0001c0001t0014g0221a0002c0002t0006g0006a0002c0002t0006g0048others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2495+529G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895466 | ||||||
| chr22:41895528
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2495+591C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895528 | ||||||
| chr22:41895588
|
A | G | 1 | a0002c0002t0001g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2495+651A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895588 | ||||||
| chr22:41895675
|
A | G | 26 | a0001c0001t0004g0245a0002c0018t0004g0159a0003c0003t0004g0097others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.2495+738A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895675 | ||||||
| chr22:41895687
|
C | T | 1 | a0004c0004t0006g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2495+750C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895687 | ||||||
| chr22:41895728
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2495+791G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895728 | ||||||
| chr22:41895852
|
G | A | 24 | a0001c0001t0004g0245a0002c0018t0004g0159a0003c0003t0004g0097others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.2495+915G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895852 | ||||||
| chr22:41895852
|
G | C | 2 | a0003c0003t0004g0135a0003c0003t0004g0137 | 2 | HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2495+915G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41895852 | ||||||
| chr22:41895875
|
C | CA | 14 | a0001c0001t0005g0018a0001c0001t0014g0221a0002c0002t0005g0014others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2495+939dupA | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr22 | 41895875 | |||||
| chr22:41896073
|
G | A | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2496-979G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896073 | ||||||
| chr22:41896106
|
A | G | 1 | a0004c0004t0010g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2496-946A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896106 | ||||||
| chr22:41896109
|
C | G | 14 | a0001c0001t0005g0018a0001c0001t0014g0221a0002c0002t0005g0014others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2496-943C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896109 | ||||||
| chr22:41896274
|
A | C | 30 | a0001c0001t0005g0018a0001c0001t0008g0112a0001c0001t0008g0243others(27): Show | 30 | HG00639.hp2 HG01109.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.2496-778A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896274 | ||||||
| chr22:41896363
|
T | G | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2496-689T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896363 | ||||||
| chr22:41896487
|
G | A | 1 | a0001c0001t0004g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2496-565G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896487 | ||||||
| chr22:41896655
|
G | A | 1 | a0008c0014t0006g0023 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2496-397G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896655 | ||||||
| chr22:41896739
|
G | A | 4 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0322others(1): Show | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2496-313G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896739 | ||||||
| chr22:41896881
|
C | T | 25 | a0003c0003t0004g0097a0003c0003t0004g0105a0003c0003t0004g0116others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.2496-171C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896881 | ||||||
| chr22:41896892
|
C | T | 3 | a0003c0003t0004g0116a0003c0010t0001g0145a0005c0006t0004g0241 | 3 | HG00280.hp1 NA18952.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.2496-160C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896892 | ||||||
| chr22:41896918
|
C | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0204 | 2 | HG02027.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.2496-134C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896918 | ||||||
| chr22:41896919
|
G | A | 24 | a0003c0003t0004g0097a0003c0003t0004g0105a0003c0003t0004g0116others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2496-133G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41896919 | ||||||
| chr22:41897011
|
A | G | 1 | a0002c0002t0006g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2496-41A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 13/18 | chr22 | 41897011 | ||||||
| chr22:41897274
|
A | G | 12 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2605+113A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41897274 | ||||||
| chr22:41897431
|
G | T | 1 | a0001c0001t0003g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2605+270G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41897431 | ||||||
| chr22:41898113
|
T | A | 6 | a0002c0002t0003g0008a0002c0002t0003g0055a0002c0002t0003g0056others(3): Show | 6 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2606-536T>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898113 | ||||||
| chr22:41898119
|
A | AT | 14 | a0001c0001t0005g0018a0001c0001t0014g0221a0002c0002t0005g0014others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2606-522dupT | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr22 | 41898119 | |||||
| chr22:41898133
|
G | A | 3 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244 | 3 | HG03041.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2606-516G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898133 | ||||||
| chr22:41898172
|
A | G | 58 | a0001c0001t0001g0299a0001c0001t0004g0245a0001c0001t0005g0018others(55): Show | 58 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.2606-477A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898172 | ||||||
| chr22:41898249
|
G | T | 1 | a0001c0001t0001g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2606-400G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898249 | ||||||
| chr22:41898334
|
T | C | 14 | a0001c0001t0005g0018a0001c0001t0014g0221a0002c0002t0005g0014others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2606-315T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898334 | ||||||
| chr22:41898609
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2606-40C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 14/18 | chr22 | 41898609 | ||||||
| chr22:41898867
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2738+86G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41898867 | ||||||
| chr22:41899174
|
A | G | 5 | a0002c0002t0002g0117a0002c0002t0002g0147a0002c0002t0002g0148others(2): Show | 5 | HG00642.hp2 HG02735.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.2738+393A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899174 | ||||||
| chr22:41899246
|
C | G | 85 | a0001c0001t0001g0094a0001c0001t0001g0126a0001c0001t0001g0165others(82): Show | 85 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2738+465C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899246 | ||||||
| chr22:41899507
|
C | T | 4 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0322others(1): Show | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2738+726C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899507 | ||||||
| chr22:41899604
|
C | T | 1 | a0001c0001t0004g0245 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2739-726C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899604 | ||||||
| chr22:41899649
|
G | A | 24 | a0002c0018t0004g0159a0003c0003t0004g0097a0003c0003t0004g0105others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2739-681G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899649 | ||||||
| chr22:41899753
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0001g0276 | 2 | NA18939.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.2739-577C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899753 | ||||||
| chr22:41899965
|
G | T | 2 | a0001c0001t0013g0220a0002c0002t0013g0054 | 2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2739-365G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899965 | ||||||
| chr22:41899966
|
G | C | 23 | a0002c0018t0004g0159a0003c0003t0004g0097a0003c0003t0004g0105others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2739-364G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899966 | ||||||
| chr22:41899988
|
G | A | 1 | a0001c0012t0001g0312 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2739-342G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41899988 | ||||||
| chr22:41900138
|
G | A | 12 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2739-192G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41900138 | ||||||
| chr22:41900175
|
G | C | 13 | a0001c0001t0004g0245a0001c0001t0008g0112a0001c0001t0008g0243others(10): Show | 13 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2739-155G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41900175 | ||||||
| chr22:41900218
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2739-112G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 15/18 | chr22 | 41900218 | ||||||
| chr22:41900580
|
C | G | 10 | a0002c0002t0002g0047a0002c0002t0002g0067a0002c0002t0002g0078others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2907+82C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41900580 | ||||||
| chr22:41900604
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2907+106C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41900604 | ||||||
| chr22:41900699
|
T | C | 57 | a0001c0001t0004g0245a0001c0001t0005g0018a0001c0001t0008g0112others(54): Show | 57 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2907+201T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41900699 | ||||||
| chr22:41900929
|
C | T | 13 | a0001c0001t0004g0245a0001c0001t0008g0112a0001c0001t0008g0243others(10): Show | 13 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2907+431C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41900929 | ||||||
| chr22:41901187
|
T | G | 6 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0205others(3): Show | 6 | HG00673.hp2 NA18953.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.2907+689T>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901187 | ||||||
| chr22:41901210
|
G | A | 14 | a0001c0001t0005g0018a0001c0001t0014g0221a0002c0002t0005g0014others(11): Show | 14 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.2907+712G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901210 | ||||||
| chr22:41901298
|
G | T | 4 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0322others(1): Show | 4 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2907+800G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901298 | ||||||
| chr22:41901459
|
G | A | 12 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.2907+961G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901459 | ||||||
| chr22:41901748
|
G | A | 10 | a0002c0002t0002g0047a0002c0002t0002g0067a0002c0002t0002g0078others(7): Show | 10 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2908-1222G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901748 | ||||||
| chr22:41901768
|
G | A | 1 | a0002c0002t0006g0006 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2908-1202G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901768 | ||||||
| chr22:41901918
|
G | A | 23 | a0002c0018t0004g0159a0003c0003t0004g0097a0003c0003t0004g0105others(20): Show | 23 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.2908-1052G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901918 | ||||||
| chr22:41901937
|
T | C | 1 | a0001c0024t0001g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2908-1033T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901937 | ||||||
| chr22:41901964
|
T | C | 56 | a0001c0001t0004g0245a0001c0001t0005g0018a0001c0001t0008g0112others(53): Show | 56 | HG00099.hp1 HG00280.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2908-1006T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41901964 | ||||||
| chr22:41902095
|
A | T | 2 | a0001c0001t0003g0010a0002c0002t0003g0109 | 2 | HG01496.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2908-875A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902095 | ||||||
| chr22:41902161
|
C | T | 24 | a0002c0018t0004g0159a0003c0003t0004g0097a0003c0003t0004g0105others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2908-809C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902161 | ||||||
| chr22:41902227
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2908-743C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902227 | ||||||
| chr22:41902342
|
G | A | 1 | a0002c0002t0005g0015 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2908-628G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902342 | ||||||
| chr22:41902392
|
G | T | 1 | a0001c0001t0001g0005 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2908-578G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902392 | ||||||
| chr22:41902397
|
A | T | 1 | a0002c0005t0016g0251 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2908-573A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902397 | ||||||
| chr22:41902400
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2908-570C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902400 | ||||||
| chr22:41902403
|
A | T | 1 | a0003c0010t0022g0022 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2908-567A>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902403 | ||||||
| chr22:41902410
|
G | T | 1 | a0001c0001t0001g0301 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2908-560G>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902410 | ||||||
| chr22:41902534
|
A | C | 4 | a0002c0005t0007g0012a0002c0005t0007g0248a0002c0005t0007g0250others(1): Show | 4 | HG02486.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2908-436A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902534 | ||||||
| chr22:41902582
|
T | C | 1 | a0008c0014t0006g0023 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2908-388T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902582 | ||||||
| chr22:41902597
|
C | T | 24 | a0002c0018t0004g0159a0003c0003t0004g0097a0003c0003t0004g0105others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2908-373C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902597 | ||||||
| chr22:41902678
|
G | A | 3 | a0002c0002t0003g0329a0002c0002t0003g0330a0002c0002t0003g0331 | 3 | HG03225.hp1 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2908-292G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902678 | ||||||
| chr22:41902771
|
C | T | 5 | a0001c0001t0001g0255a0001c0001t0001g0287a0001c0001t0001g0301others(2): Show | 5 | NA18973.hp1 NA18988.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.2908-199C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902771 | ||||||
| chr22:41902820
|
G | A | 3 | a0002c0002t0001g0038a0002c0002t0001g0039a0002c0002t0001g0040 | 3 | HG01934.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2908-150G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902820 | ||||||
| chr22:41902822
|
C | T | 1 | a0003c0003t0004g0135 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2908-148C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902822 | ||||||
| chr22:41902902
|
G | A | 1 | a0003c0003t0004g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2908-68G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 16/18 | chr22 | 41902902 | ||||||
| chr22:41903173
|
G | C | 1 | a0003c0003t0004g0130 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3093+18G>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903173 | ||||||
| chr22:41903417
|
CAG | C | 7 | a0002c0002t0009g0320a0002c0002t0009g0321a0002c0002t0009g0322others(4): Show | 7 | HG00099.hp1 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.3093+263_3093+264d others(4): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903417 | ||||||
| chr22:41903522
|
T | C | 7 | a0002c0002t0001g0118a0002c0002t0001g0150a0002c0002t0001g0151others(4): Show | 7 | NA18965.hp2 NA18980.hp1 NA18990.hp2 others(4): Show |
intron_variant | MODIFIER | c.3093+367T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903522 | ||||||
| chr22:41903531
|
A | G | 53 | a0001c0001t0002g0257a0001c0001t0002g0327a0001c0001t0015g0319others(50): Show | 54 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.3093+376A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903531 | ||||||
| chr22:41903806
|
G | A | 12 | a0001c0001t0008g0112a0001c0001t0008g0243a0001c0001t0008g0244others(9): Show | 12 | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3093+651G>A | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903806 | ||||||
| chr22:41903813
|
T | C | 30 | a0001c0001t0004g0245a0002c0002t0009g0320a0002c0002t0009g0321others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.3093+658T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41903813 | ||||||
| chr22:41904058
|
A | G | 26 | a0001c0001t0005g0018a0001c0001t0008g0112a0001c0001t0008g0243others(23): Show | 26 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3094-805A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904058 | ||||||
| chr22:41904169
|
C | T | 26 | a0001c0001t0005g0018a0001c0001t0008g0112a0001c0001t0008g0243others(23): Show | 26 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.3094-694C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904169 | ||||||
| chr22:41904200
|
A | C | 2 | a0001c0001t0013g0220a0002c0002t0013g0054 | 2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3094-663A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904200 | ||||||
| chr22:41904244
|
C | G | 29 | a0001c0001t0004g0245a0002c0002t0009g0320a0002c0002t0009g0321others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.3094-619C>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904244 | ||||||
| chr22:41904407
|
C | T | 5 | a0001c0001t0004g0245a0002c0002t0009g0320a0002c0002t0009g0321others(2): Show | 5 | HG01109.hp2 HG02970.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.3094-456C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904407 | ||||||
| chr22:41904424
|
TCTTC | T | 24 | a0002c0018t0004g0159a0003c0003t0004g0097a0003c0003t0004g0105others(21): Show | 24 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.3094-435_3094-432d others(6): Show |
SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr22 | 41904424 | |||||
| chr22:41904470
|
A | C | 1 | a0004c0004t0006g0049 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3094-393A>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 17/18 | chr22 | 41904470 | ||||||
| chr22:41905010
|
A | G | 39 | a0001c0001t0004g0245a0001c0001t0008g0112a0001c0001t0008g0243others(36): Show | 39 | HG00099.hp1 HG00280.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.3205+36A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905010 | ||||||
| chr22:41905129
|
T | C | 54 | a0001c0001t0002g0257a0001c0001t0002g0327a0001c0001t0015g0319others(51): Show | 55 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.3205+155T>C | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905129 | ||||||
| chr22:41905153
|
A | G | 1 | a0002c0002t0008g0332 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3205+179A>G | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905153 | ||||||
| chr22:41905328
|
C | T | 7 | a0001c0001t0001g0171a0001c0001t0001g0180a0001c0001t0001g0181others(4): Show | 7 | NA18947.hp2 NA18961.hp2 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.3206-112C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905328 | ||||||
| chr22:41905430
|
C | T | 14 | a0001c0007t0003g0007a0001c0007t0003g0086a0001c0007t0003g0087others(11): Show | 14 | HG00738.hp1 HG00741.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.3206-10C>T | SREBF2 | ENSG00000198911.13 | transcript | ENST00000361204.9 | protein_coding | 18/18 | chr22 | 41905430 |