Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23231 |
|---|---|
| ensemblid | ENSG00000091490.11 |
| hgncid | 29108 |
| symbol | SEL1L3 |
| name | SEL1L family member 3 |
| refseq_nuc | NM_015187.5 |
| refseq_prot | NP_056002.2 |
| ensembl_nuc | ENST00000399878.8 |
| ensembl_prot | ENSP00000382767.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 25747433 |
| end | 25862988 |
| strand | - |
| ver | v1.2 |
| region | chr4:25747433-25862988 |
| region5000 | chr4:25742433-25867988 |
| regionname0 | SEL1L3_chr4_25747433_25862988 |
| regionname5000 | SEL1L3_chr4_25742433_25867988 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1132 | 258 | 57 | 52 | 102 | 9 | 36 | 70 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002 | 0/0 | 1132 | 22 | 20 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0003 | 0/0 | 1132 | 8 | 0 | 0 | 8 | 0 | 0 | 8 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0004 | 0/0 | 1132 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0005 | 0/0 | 1132 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0006 | 0/0 | 1132 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0007 | 0/0 | 1132 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0008 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0009 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0010 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0011 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0012 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0013 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0014 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0015 | 0/0 | 1132 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0016 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0017 | 0/0 | 1132 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0018 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0019 | 0/0 | 1132 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3399 | 230 | 37 | 49 | 99 | 9 | 34 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0002 | 0/0 | 3399 | 9 | 9 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0003 | 0/0 | 3399 | 8 | 3 | 1 | 2 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0004 | 0/0 | 3399 | 7 | 0 | 0 | 7 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0005 | 0/0 | 3399 | 6 | 4 | 2 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0006 | 0/0 | 3399 | 5 | 5 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0007 | 0/0 | 3399 | 5 | 5 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0008 | 0/0 | 3399 | 4 | 4 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0009 | 0/0 | 3399 | 4 | 4 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0010 | 0/0 | 3399 | 3 | 2 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0011 | 0/0 | 3399 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0012 | 0/0 | 3399 | 2 | 0 | 0 | 0 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0013 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0014 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0015 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0016 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0017 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0018 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0019 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0020 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0021 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0022 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0023 | 0/0 | 3399 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0024 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0025 | 0/0 | 3399 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0026 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0027 | 0/0 | 3399 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0028 | 0/0 | 3399 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0029 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0030 | 0/0 | 3399 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0031 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0032 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0033 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0034 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0035 | 0/0 | 3399 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0036 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0037 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| c0038 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1145 | 123 | 13 | 25 | 74 | 3 | 8 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0002 | 1/1 | 1145 | 120 | 43 | 21 | 24 | 6 | 24 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0003 | 0/0 | 1153 | 21 | 7 | 1 | 9 | 1 | 3 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0004 | 0/0 | 1145 | 8 | 7 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0005 | 0/0 | 1147 | 7 | 4 | 1 | 2 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0006 | 0/0 | 1143 | 5 | 5 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0007 | 0/0 | 1145 | 4 | 4 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0008 | 0/0 | 1155 | 3 | 1 | 2 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0009 | 0/0 | 1153 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0010 | 0/0 | 1145 | 2 | 1 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0011 | 0/0 | 1145 | 2 | 0 | 0 | 0 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0012 | 0/0 | 1147 | 2 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0013 | 0/0 | 1153 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0014 | 0/0 | 1145 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0015 | 0/0 | 1147 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0016 | 0/0 | 1145 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0017 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0018 | 0/0 | 1145 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0019 | 0/0 | 1145 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0020 | 0/0 | 1145 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0021 | 0/0 | 1145 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0022 | 0/0 | 1153 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0023 | 0/0 | 1145 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| t0024 | 0/0 | 1145 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3399 | 230 | 37 | 49 | 99 | 9 | 34 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0003 | 0/0 | 3399 | 8 | 3 | 1 | 2 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0006 | 0/0 | 3399 | 5 | 5 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0008 | 0/0 | 3399 | 4 | 4 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0010 | 0/0 | 3399 | 3 | 2 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0011 | 0/0 | 3399 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0014 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0017 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0025 | 0/0 | 3399 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0027 | 0/0 | 3399 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0034 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0002 | 0/0 | 3399 | 9 | 9 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0005 | 0/0 | 3399 | 6 | 4 | 2 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0009 | 0/0 | 3399 | 4 | 4 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0013 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0015 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0018 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0003c0004 | 0/0 | 3399 | 7 | 0 | 0 | 7 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0003c0028 | 0/0 | 3399 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0004c0007 | 0/0 | 3399 | 5 | 5 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0005c0019 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0005c0021 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0005c0022 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0006c0012 | 0/0 | 3399 | 2 | 0 | 0 | 0 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0007c0031 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0007c0033 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0008c0038 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0009c0036 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0010c0037 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0011c0029 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0012c0016 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0013c0026 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0014c0024 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0015c0023 | 0/0 | 3399 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0016c0020 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0017c0030 | 0/0 | 3399 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0018c0032 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0019c0035 | 0/0 | 3399 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4543 | 102 | 6 | 22 | 63 | 3 | 8 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0002 | 1/1 | 4543 | 92 | 22 | 20 | 22 | 5 | 21 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0003 | 0/0 | 4551 | 16 | 2 | 1 | 9 | 1 | 3 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0004 | 0/0 | 4543 | 2 | 1 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0005 | 0/0 | 4545 | 5 | 2 | 1 | 2 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0006 | 0/0 | 4541 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0008 | 0/0 | 4553 | 2 | 0 | 2 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0009 | 0/0 | 4551 | 2 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0010 | 0/0 | 4543 | 2 | 1 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0011 | 0/0 | 4543 | 2 | 0 | 0 | 0 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0016 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0017 | 0/0 | 4545 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0018 | 0/0 | 4543 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0001t0021 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0003t0002 | 0/0 | 4543 | 7 | 2 | 1 | 2 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0003t0009 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0006t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0006t0004 | 0/0 | 4543 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0006t0007 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0008t0001 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0008t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0008t0007 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0008t0012 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0010t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0010t0022 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0010t0024 | 0/0 | 4543 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0011t0002 | 0/0 | 4543 | 2 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0011t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0014t0001 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0017t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0025t0001 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0027t0001 | 0/0 | 4543 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0001c0034t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0002t0001 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0002t0002 | 0/0 | 4543 | 5 | 5 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0002t0005 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0002t0006 | 0/0 | 4541 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0002t0008 | 0/0 | 4553 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0005t0001 | 0/0 | 4543 | 2 | 0 | 2 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0005t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0005t0006 | 0/0 | 4541 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0009t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0009t0004 | 0/0 | 4543 | 2 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0009t0007 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0013t0014 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0015t0001 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0002c0018t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0003c0004t0001 | 0/0 | 4543 | 7 | 0 | 0 | 7 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0003c0028t0001 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0004c0007t0001 | 0/0 | 4543 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0004c0007t0002 | 0/0 | 4543 | 2 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0005c0019t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0005c0021t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0005c0022t0004 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0006c0012t0002 | 0/0 | 4543 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0006c0012t0015 | 0/0 | 4545 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0007c0031t0020 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0007c0033t0007 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0008c0038t0012 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0009c0036t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0010c0037t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0011c0029t0005 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0012c0016t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0013c0026t0013 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0014c0024t0023 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0015c0023t0002 | 0/0 | 4543 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0016c0020t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0017c0030t0001 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0018c0032t0019 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| a0019c0035t0001 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | copy fasta | chr4 | 25742433 | 25867988 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0008g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0010g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0011g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0016g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0017g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0018g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0001t0021g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0003t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0003t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0003t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0003t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0003t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0006t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0006t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0006t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0006t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0006t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0008t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0008t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0008t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0008t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0010t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0010t0022g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0010t0024g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0011t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0011t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0011t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0014t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0017t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0025t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0027t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0001c0034t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0002t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0002t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0002t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0005t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0005t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0005t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0005t0006g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0009t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0009t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0009t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0009t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0013t0014g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0015t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0002c0018t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0003c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0003c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0003c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0003c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0003c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0003c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0003c0028t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0004c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0004c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0004c0007t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0004c0007t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0004c0007t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0005c0019t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0005c0021t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0005c0022t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0006c0012t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0006c0012t0015g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0007c0031t0020g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0007c0033t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0008c0038t0012g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0009c0036t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0010c0037t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0011c0029t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0012c0016t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0013c0026t0013g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0014c0024t0023g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0015c0023t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0016c0020t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0017c0030t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0018c0032t0019g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| a0019c0035t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | GBR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0046 | EUR | GBR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | GBR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00558 | hp2 | a0001 | c0003 | t0002 | g0103 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00609 | hp1 | a0001 | c0003 | t0002 | g0049 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00733 | hp2 | a0001 | c0027 | t0001 | g0197 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00741 | hp1 | a0001 | c0001 | t0010 | g0129 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01070 | hp1 | a0002 | c0005 | t0001 | g0156 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01071 | hp2 | a0002 | c0005 | t0001 | g0157 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0114 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0024 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01109 | hp1 | a0001 | c0010 | t0024 | g0309 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01192 | hp1 | a0001 | c0001 | t0018 | g0233 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0123 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01257 | hp2 | a0001 | c0001 | t0008 | g0290 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | IBS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01515 | hp2 | a0015 | c0023 | t0002 | g0181 | EUR | IBS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0244 | EUR | IBS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0285 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02055 | hp2 | a0005 | c0019 | t0002 | g0010 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02074 | hp2 | a0001 | c0001 | t0021 | g0306 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02145 | hp2 | a0010 | c0037 | t0003 | g0304 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02257 | hp1 | a0002 | c0005 | t0006 | g0001 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02258 | hp1 | a0002 | c0009 | t0007 | g0298 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02258 | hp2 | a0012 | c0016 | t0002 | g0141 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02280 | hp1 | a0001 | c0003 | t0009 | g0027 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02280 | hp2 | a0002 | c0009 | t0004 | g0269 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0063 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02451 | hp2 | a0001 | c0006 | t0004 | g0299 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02572 | hp1 | a0002 | c0009 | t0003 | g0278 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02615 | hp2 | a0001 | c0006 | t0004 | g0132 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02622 | hp2 | a0001 | c0006 | t0004 | g0092 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02630 | hp1 | a0001 | c0017 | t0002 | g0144 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0133 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02647 | hp2 | a0001 | c0011 | t0002 | g0055 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02717 | hp1 | a0005 | c0022 | t0004 | g0284 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02717 | hp2 | a0011 | c0029 | t0005 | g0135 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02723 | hp2 | a0001 | c0011 | t0002 | g0101 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02735 | hp1 | a0006 | c0012 | t0002 | g0022 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02738 | hp2 | a0001 | c0003 | t0002 | g0025 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02809 | hp1 | a0016 | c0020 | t0002 | g0011 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02809 | hp2 | a0002 | c0002 | t0008 | g0301 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0277 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02818 | hp2 | a0001 | c0008 | t0002 | g0142 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0096 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02897 | hp2 | a0001 | c0003 | t0002 | g0097 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02922 | hp2 | a0005 | c0021 | t0003 | g0283 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02965 | hp1 | a0004 | c0007 | t0001 | g0165 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02965 | hp2 | a0002 | c0002 | t0006 | g0268 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02970 | hp1 | a0004 | c0007 | t0001 | g0166 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02970 | hp2 | a0001 | c0006 | t0002 | g0154 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02976 | hp1 | a0001 | c0001 | t0009 | g0124 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02976 | hp2 | a0001 | c0034 | t0002 | g0137 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03041 | hp1 | a0001 | c0010 | t0002 | g0173 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03041 | hp2 | a0001 | c0010 | t0022 | g0307 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03098 | hp1 | a0001 | c0014 | t0001 | g0159 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03098 | hp2 | a0009 | c0036 | t0002 | g0303 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03130 | hp1 | a0002 | c0005 | t0006 | g0001 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0281 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03209 | hp1 | a0007 | c0031 | t0020 | g0169 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03209 | hp2 | a0001 | c0006 | t0007 | g0125 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03453 | hp1 | a0013 | c0026 | t0013 | g0280 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03453 | hp2 | a0002 | c0015 | t0001 | g0160 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03486 | hp1 | a0004 | c0007 | t0002 | g0168 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03486 | hp2 | a0008 | c0038 | t0012 | g0305 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03516 | hp1 | a0001 | c0008 | t0001 | g0162 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03516 | hp2 | a0002 | c0009 | t0004 | g0267 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0282 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03579 | hp2 | a0002 | c0002 | t0005 | g0187 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03654 | hp2 | a0006 | c0012 | t0015 | g0073 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03704 | hp1 | a0001 | c0003 | t0002 | g0013 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03942 | hp1 | a0001 | c0001 | t0011 | g0004 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04184 | hp1 | a0001 | c0001 | t0011 | g0005 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0086 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0138 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18522 | hp2 | a0002 | c0005 | t0003 | g0122 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18906 | hp1 | a0007 | c0033 | t0007 | g0171 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18941 | hp2 | a0003 | c0004 | t0001 | g0228 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18954 | hp1 | a0001 | c0025 | t0001 | g0241 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18954 | hp2 | a0003 | c0028 | t0001 | g0185 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18968 | hp1 | a0003 | c0004 | t0001 | g0110 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18969 | hp1 | a0003 | c0004 | t0001 | g0195 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18973 | hp2 | a0001 | c0001 | t0017 | g0090 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19011 | hp1 | a0001 | c0001 | t0016 | g0091 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19030 | hp1 | a0018 | c0032 | t0019 | g0170 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19030 | hp2 | a0002 | c0013 | t0014 | g0127 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19043 | hp2 | a0001 | c0011 | t0003 | g0172 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19057 | hp1 | a0003 | c0004 | t0001 | g0210 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19064 | hp2 | a0003 | c0004 | t0001 | g0202 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19079 | hp1 | a0003 | c0004 | t0001 | g0212 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19081 | hp1 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19086 | hp1 | a0017 | c0030 | t0001 | g0045 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19086 | hp2 | a0019 | c0035 | t0001 | g0255 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19240 | hp1 | a0002 | c0018 | t0002 | g0158 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA19240 | hp2 | a0014 | c0024 | t0023 | g0308 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ASW | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA20129 | hp2 | a0004 | c0007 | t0002 | g0167 | AFR | ASW | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0262 | EUR | TSI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | TSI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | GIH | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | GIH | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02109 | hp1 | a0002 | c0005 | t0006 | g0001 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03471 | hp1 | a0001 | c0008 | t0007 | g0161 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG06807 | hp1 | a0001 | c0008 | t0012 | g0143 | AFR | USA | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | USA | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | USA | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA21309 | hp1 | a0004 | c0007 | t0001 | g0164 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0189 | REF | REF | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0053 | REF | REF | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:25748460
|
G | A | 1 | a0013 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.3364C>T | p.Pro1122Ser | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 3516/4543 | 3364/3399 | 1122/1132 | chr4 | 25748460 | ||
| chr4:25757712
|
C | G | 1 | a0003 | 8 | NA18941.hp2 NA18954.hp2 NA18968.hp1 others(5): Show |
missense_variant | MODERATE | c.3162G>C | p.Trp1054Cys | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 22/24 | 3314/4543 | 3162/3399 | 1054/1132 | chr4 | 25757712 | ||
| chr4:25767594
|
A | G | 1 | a0018 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2776T>C | p.Tyr926His | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/24 | 2928/4543 | 2776/3399 | 926/1132 | chr4 | 25767594 | ||
| chr4:25790562
|
T | C | 2 | a0009a0012 | 2 | HG02258.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1969A>G | p.Thr657Ala | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/24 | 2121/4543 | 1969/3399 | 657/1132 | chr4 | 25790562 | ||
| chr4:25804657
|
T | C | 6 | a0002a0004a0010others(3): Show | 31 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(28): Show |
missense_variant | MODERATE | c.1660A>G | p.Ile554Val | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/24 | 1812/4543 | 1660/3399 | 554/1132 | chr4 | 25804657 | ||
| chr4:25822001
|
C | T | 1 | a0014 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1285G>A | p.Ala429Thr | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/24 | 1437/4543 | 1285/3399 | 429/1132 | chr4 | 25822001 | ||
| chr4:25833099
|
T | C | 1 | a0006 | 2 | HG02735.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.994A>G | p.Ile332Val | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/24 | 1146/4543 | 994/3399 | 332/1132 | chr4 | 25833099 | ||
| chr4:25833456
|
G | A | 1 | a0011 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.974C>T | p.Thr325Met | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 4/24 | 1126/4543 | 974/3399 | 325/1132 | chr4 | 25833456 | ||
| chr4:25833478
|
C | T | 1 | a0015 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.952G>A | p.Gly318Ser | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 4/24 | 1104/4543 | 952/3399 | 318/1132 | chr4 | 25833478 | ||
| chr4:25835256
|
G | T | 2 | a0005a0016 | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.801C>A | p.Phe267Leu | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/24 | 953/4543 | 801/3399 | 267/1132 | chr4 | 25835256 | ||
| chr4:25847330
|
G | A | 1 | a0017 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.697C>T | p.Arg233Trp | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 849/4543 | 697/3399 | 233/1132 | chr4 | 25847330 | ||
| chr4:25847707
|
T | C | 3 | a0004a0007a0018 | 8 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(5): Show |
missense_variant | MODERATE | c.320A>G | p.Gln107Arg | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 472/4543 | 320/3399 | 107/1132 | chr4 | 25847707 | ||
| chr4:25847855
|
G | A | 1 | a0019 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.172C>T | p.Pro58Ser | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 324/4543 | 172/3399 | 58/1132 | chr4 | 25847855 | ||
| chr4:25862781
|
G | A | 2 | a0009a0010 | 2 | HG02145.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.56C>T | p.Pro19Leu | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/24 | 208/4543 | 56/3399 | 19/1132 | chr4 | 25862781 | ||
| chr4:25862827
|
G | A | 1 | a0008 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.10C>T | p.Arg4Cys | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/24 | 162/4543 | 10/3399 | 4/1132 | chr4 | 25862827 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:25757690
|
G | A | 5 | a0001c0006a0001c0011a0002c0009others(2): Show | 14 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.3184C>T | p.Leu1062Leu | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 22/24 | 3336/4543 | 3184/3399 | 1062/1132 | chr4 | 25757690 | ||
| chr4:25765347
|
G | A | 2 | a0007c0031a0013c0026 | 2 | HG03209.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.2934C>T | p.Ala978Ala | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/24 | 3086/4543 | 2934/3399 | 978/1132 | chr4 | 25765347 | ||
| chr4:25779090
|
A | G | 2 | a0002c0018a0007c0031 | 2 | HG03209.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.2571T>C | p.Pro857Pro | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/24 | 2723/4543 | 2571/3399 | 857/1132 | chr4 | 25779090 | ||
| chr4:25788281
|
G | A | 2 | a0001c0010a0001c0014 | 4 | HG01109.hp1 HG03041.hp1 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.2160C>T | p.Gly720Gly | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/24 | 2312/4543 | 2160/3399 | 720/1132 | chr4 | 25788281 | ||
| chr4:25804697
|
C | T | 1 | a0001c0027 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.1620G>A | p.Lys540Lys | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/24 | 1772/4543 | 1620/3399 | 540/1132 | chr4 | 25804697 | ||
| chr4:25804727
|
T | C | 2 | a0005c0021a0005c0022 | 2 | HG02717.hp1 HG02922.hp2 |
synonymous_variant | LOW | c.1590A>G | p.Val530Val | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/24 | 1742/4543 | 1590/3399 | 530/1132 | chr4 | 25804727 | ||
| chr4:25819875
|
A | G | 1 | a0001c0025 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.1356T>C | p.Ala452Ala | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/24 | 1508/4543 | 1356/3399 | 452/1132 | chr4 | 25819875 | ||
| chr4:25822002
|
G | A | 7 | a0001c0003a0001c0011a0001c0017others(4): Show | 16 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(13): Show |
synonymous_variant | LOW | c.1284C>T | p.Pro428Pro | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/24 | 1436/4543 | 1284/3399 | 428/1132 | chr4 | 25822002 | ||
| chr4:25833109
|
G | A | 2 | a0002c0005a0002c0018 | 7 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.984C>T | p.Gly328Gly | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/24 | 1136/4543 | 984/3399 | 328/1132 | chr4 | 25833109 | ||
| chr4:25847361
|
A | G | 7 | a0001c0008a0001c0014a0001c0017others(4): Show | 15 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(12): Show |
synonymous_variant | LOW | c.666T>C | p.Leu222Leu | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 818/4543 | 666/3399 | 222/1132 | chr4 | 25847361 | ||
| chr4:25847727
|
C | T | 1 | a0002c0013 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.300G>A | p.Ser100Ser | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 452/4543 | 300/3399 | 100/1132 | chr4 | 25847727 | ||
| chr4:25847751
|
G | A | 1 | a0001c0034 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.276C>T | p.Asn92Asn | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 428/4543 | 276/3399 | 92/1132 | chr4 | 25847751 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:25747538
|
A | T | 1 | a0002c0013t0014 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*887T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 887 | chr4 | 25747538 | |||||
| chr4:25747574
|
T | A | 1 | a0007c0031t0020 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*851A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 851 | chr4 | 25747574 | |||||
| chr4:25747576
|
T | A | 1 | a0007c0031t0020 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 849 | chr4 | 25747576 | |||||
| chr4:25747577
|
A | AAC | 7 | a0001c0001t0005a0001c0001t0017a0001c0008t0012others(4): Show | 11 | HG02293.hp2 HG02717.hp2 HG02922.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*846_*847dupGT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 847 | chr4 | 25747577 | |||||
| chr4:25747577
|
A | AACACACA others(1): Show |
10 | a0001c0001t0003a0001c0001t0009a0001c0003t0009others(7): Show | 26 | HG00438.hp1 HG01081.hp1 HG01516.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*840_*847dupGTGTGT others(2): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 847 | chr4 | 25747577 | |||||
| chr4:25747577
|
A | AACACACA others(3): Show |
2 | a0001c0001t0008a0002c0002t0008 | 3 | HG01074.hp1 HG01257.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*838_*847dupGTGTGT others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 847 | chr4 | 25747577 | |||||
| chr4:25747577
|
A | C | 1 | a0007c0031t0020 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*848T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 848 | chr4 | 25747577 | |||||
| chr4:25747577
|
AAC | A | 3 | a0001c0001t0006a0002c0002t0006a0002c0005t0006 | 5 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*846_*847delGT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 846 | chr4 | 25747577 | |||||
| chr4:25747605
|
T | C | 1 | a0006c0012t0015 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*820A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 820 | chr4 | 25747605 | |||||
| chr4:25747623
|
C | T | 1 | a0001c0001t0016 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*802G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 802 | chr4 | 25747623 | |||||
| chr4:25747663
|
C | T | 6 | a0001c0006t0007a0001c0008t0007a0001c0008t0012others(3): Show | 6 | HG02258.hp1 HG03209.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*762G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 762 | chr4 | 25747663 | |||||
| chr4:25747681
|
C | A | 20 | a0001c0001t0001a0001c0001t0010a0001c0001t0016others(17): Show | 131 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*744G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 744 | chr4 | 25747681 | |||||
| chr4:25747797
|
T | C | 1 | a0001c0001t0018 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*628A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 628 | chr4 | 25747797 | |||||
| chr4:25747865
|
C | T | 2 | a0001c0008t0012a0008c0038t0012 | 2 | HG03486.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*560G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 560 | chr4 | 25747865 | |||||
| chr4:25747886
|
A | G | 1 | a0013c0026t0013 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*539T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 539 | chr4 | 25747886 | |||||
| chr4:25748000
|
C | T | 1 | a0013c0026t0013 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*425G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 425 | chr4 | 25748000 | |||||
| chr4:25748038
|
C | G | 1 | a0001c0001t0011 | 2 | HG03942.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*387G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 387 | chr4 | 25748038 | |||||
| chr4:25748065
|
G | A | 1 | a0018c0032t0019 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 360 | chr4 | 25748065 | |||||
| chr4:25748128
|
T | G | 3 | a0001c0001t0009a0001c0003t0009a0007c0031t0020 | 4 | HG01891.hp1 HG02280.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*297A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 297 | chr4 | 25748128 | |||||
| chr4:25748268
|
G | C | 4 | a0001c0001t0004a0001c0006t0004a0002c0009t0004others(1): Show | 8 | HG01192.hp2 HG02280.hp2 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*157C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 157 | chr4 | 25748268 | |||||
| chr4:25748378
|
C | T | 1 | a0001c0001t0010 | 2 | HG00741.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*47G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 47 | chr4 | 25748378 | |||||
| chr4:25862876
|
G | C | 1 | a0001c0001t0021 | 1 | HG02074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/24 | 40 | chr4 | 25862876 | |||||
| chr4:25862977
|
G | A | 3 | a0001c0010t0022a0001c0010t0024a0014c0024t0023 | 3 | HG01109.hp1 HG03041.hp2 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-141C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/24 | 141 | chr4 | 25862977 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:25748596
|
T | A | 3 | a0001c0001t0002g0003a0001c0003t0002g0013a0006c0012t0015g0073 | 3 | HG03654.hp1 HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3260-32A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748596 | ||||||
| chr4:25748639
|
C | G | 65 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(62): Show | 65 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.3260-75G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748639 | ||||||
| chr4:25748685
|
T | G | 3 | a0001c0001t0003g0149a0001c0010t0022g0307a0002c0005t0003g0122 | 3 | HG03041.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3260-121A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748685 | ||||||
| chr4:25748846
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3260-282T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748846 | ||||||
| chr4:25748867
|
T | C | 94 | a0001c0001t0001g0293a0001c0001t0002g0002a0001c0001t0002g0014others(91): Show | 97 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.3260-303A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748867 | ||||||
| chr4:25748912
|
C | T | 15 | a0001c0001t0002g0052a0001c0001t0002g0102a0001c0001t0002g0106others(12): Show | 15 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.3260-348G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748912 | ||||||
| chr4:25748964
|
G | C | 3 | a0001c0001t0003g0286a0001c0011t0003g0172a0002c0009t0003g0278 | 3 | HG02572.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3260-400C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748964 | ||||||
| chr4:25749184
|
C | T | 4 | a0001c0001t0001g0213a0001c0001t0001g0224a0001c0001t0001g0237others(1): Show | 4 | HG02004.hp2 HG02148.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.3260-620G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749184 | ||||||
| chr4:25749205
|
G | A | 2 | a0002c0005t0001g0156a0002c0005t0001g0157 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3260-641C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749205 | ||||||
| chr4:25749227
|
T | G | 93 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(90): Show | 95 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(92): Show |
intron_variant | MODIFIER | c.3260-663A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749227 | ||||||
| chr4:25749495
|
G | A | 1 | a0016c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3260-931C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749495 | ||||||
| chr4:25749594
|
T | C | 288 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(285): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.3260-1030A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749594 | ||||||
| chr4:25749656
|
T | C | 286 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(283): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.3260-1092A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749656 | ||||||
| chr4:25749746
|
G | A | 1 | a0013c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3260-1182C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749746 | ||||||
| chr4:25749807
|
T | C | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3260-1243A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749807 | ||||||
| chr4:25749821
|
G | A | 7 | a0001c0001t0003g0149a0001c0001t0010g0008a0001c0001t0010g0129others(4): Show | 7 | HG00741.hp1 HG02630.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.3260-1257C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749821 | ||||||
| chr4:25750008
|
C | A | 1 | a0001c0001t0017g0090 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3260-1444G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750008 | ||||||
| chr4:25750234
|
CA | C | 153 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(150): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.3260-1671delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750234 | ||||||
| chr4:25750234
|
CAAAAAAA others(6): Show |
C | 72 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(69): Show | 72 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.3260-1683_3260-167 others(17): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750234 | ||||||
| chr4:25750306
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3260-1742T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750306 | ||||||
| chr4:25750450
|
G | A | 61 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0040others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.3260-1886C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750450 | ||||||
| chr4:25750728
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3260-2164G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750728 | ||||||
| chr4:25750735
|
C | G | 1 | a0001c0006t0004g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3260-2171G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750735 | ||||||
| chr4:25750805
|
A | T | 1 | a0001c0006t0004g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3260-2241T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750805 | ||||||
| chr4:25750892
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3260-2328C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750892 | ||||||
| chr4:25751315
|
A | T | 2 | a0001c0001t0002g0295a0010c0037t0003g0304 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3260-2751T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751315 | ||||||
| chr4:25751374
|
C | A | 2 | a0002c0002t0005g0187a0004c0007t0002g0168 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3260-2810G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751374 | ||||||
| chr4:25751378
|
T | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0220 | 2 | HG00738.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.3260-2814A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751378 | ||||||
| chr4:25751396
|
C | T | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3260-2832G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751396 | ||||||
| chr4:25751429
|
C | T | 43 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0016others(40): Show | 44 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.3260-2865G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751429 | ||||||
| chr4:25751439
|
A | G | 238 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(235): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.3260-2875T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751439 | ||||||
| chr4:25751478
|
A | G | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3260-2914T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751478 | ||||||
| chr4:25751511
|
C | T | 4 | a0001c0001t0010g0008a0001c0001t0010g0129a0001c0008t0012g0143others(1): Show | 4 | HG00741.hp1 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3260-2947G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751511 | ||||||
| chr4:25751613
|
C | T | 2 | a0001c0008t0001g0162a0002c0002t0001g0279 | 2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3260-3049G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751613 | ||||||
| chr4:25751625
|
A | G | 21 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0193others(18): Show | 21 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.3260-3061T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751625 | ||||||
| chr4:25751671
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3260-3107C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751671 | ||||||
| chr4:25751754
|
T | C | 14 | a0001c0001t0001g0293a0001c0001t0002g0140a0001c0001t0002g0196others(11): Show | 16 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.3260-3190A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751754 | ||||||
| chr4:25751832
|
T | C | 238 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(235): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.3260-3268A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751832 | ||||||
| chr4:25751877
|
A | G | 124 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(121): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.3260-3313T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751877 | ||||||
| chr4:25751983
|
T | C | 238 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(235): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.3260-3419A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751983 | ||||||
| chr4:25752024
|
G | A | 3 | a0001c0001t0001g0206a0001c0008t0001g0162a0002c0002t0001g0279 | 3 | HG02895.hp1 HG03516.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3260-3460C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752024 | ||||||
| chr4:25752041
|
G | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0112others(16): Show | 19 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(16): Show |
intron_variant | MODIFIER | c.3260-3477C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752041 | ||||||
| chr4:25752087
|
C | T | 2 | a0001c0001t0010g0008a0001c0001t0010g0129 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3260-3523G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752087 | ||||||
| chr4:25752088
|
G | A | 3 | a0001c0001t0002g0131a0001c0001t0005g0209a0001c0001t0005g0223 | 3 | HG02257.hp2 NA18939.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.3260-3524C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752088 | ||||||
| chr4:25752108
|
C | CA | 6 | a0001c0001t0001g0047a0001c0008t0001g0162a0002c0002t0001g0279others(3): Show | 6 | HG02056.hp1 HG02895.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3260-3545dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | ||||||
| chr4:25752108
|
C | CAA | 11 | a0001c0001t0001g0293a0001c0001t0002g0140a0001c0001t0002g0196others(8): Show | 13 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3260-3546_3260-354 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | ||||||
| chr4:25752108
|
C | CAAA | 9 | a0001c0006t0007g0125a0001c0011t0003g0172a0002c0002t0005g0187others(6): Show | 9 | HG02258.hp1 HG02572.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.3260-3547_3260-354 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | ||||||
| chr4:25752108
|
C | CAAAAA | 60 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0042others(57): Show | 60 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.3260-3549_3260-354 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | ||||||
| chr4:25752108
|
C | CAAAAAA | 24 | a0001c0001t0001g0012a0001c0001t0001g0204a0001c0001t0001g0206others(21): Show | 24 | HG01106.hp2 HG01256.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.3260-3550_3260-354 others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | ||||||
| chr4:25752108
|
CA | C | 13 | a0001c0001t0001g0077a0001c0001t0001g0253a0001c0001t0002g0052others(10): Show | 13 | HG00558.hp2 HG01070.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.3260-3545delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | ||||||
| chr4:25752188
|
G | A | 3 | a0001c0001t0002g0067a0001c0001t0002g0177a0001c0001t0002g0226 | 3 | NA18941.hp1 NA19012.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3260-3624C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752188 | ||||||
| chr4:25752335
|
T | A | 87 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(84): Show | 87 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(84): Show |
intron_variant | MODIFIER | c.3260-3771A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752335 | ||||||
| chr4:25752404
|
G | A | 98 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(95): Show | 100 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(97): Show |
intron_variant | MODIFIER | c.3260-3840C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752404 | ||||||
| chr4:25752418
|
G | GA | 39 | a0001c0001t0001g0206a0001c0001t0001g0293a0001c0001t0002g0139others(36): Show | 41 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.3260-3855dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752418 | ||||||
| chr4:25752418
|
G | GAA | 23 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0193others(20): Show | 23 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.3260-3856_3260-385 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752418 | ||||||
| chr4:25752418
|
GA | G | 117 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(114): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.3260-3855delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752418 | ||||||
| chr4:25752418
|
GAA | G | 7 | a0001c0001t0001g0040a0001c0001t0001g0296a0001c0001t0003g0194others(4): Show | 7 | HG01884.hp1 HG02040.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3260-3856_3260-385 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752418 | ||||||
| chr4:25752441
|
T | G | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3260-3877A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752441 | ||||||
| chr4:25752444
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3260-3880T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752444 | ||||||
| chr4:25752782
|
C | T | 7 | a0001c0001t0002g0163a0001c0001t0002g0259a0001c0001t0002g0297others(4): Show | 7 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3260-4218G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752782 | ||||||
| chr4:25752804
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0221a0001c0001t0002g0014 | 3 | HG01261.hp2 HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3260-4240T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752804 | ||||||
| chr4:25752898
|
C | A | 6 | a0001c0011t0003g0172a0002c0002t0005g0187a0002c0009t0003g0278others(3): Show | 6 | HG02572.hp1 HG03453.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3260-4334G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752898 | ||||||
| chr4:25752904
|
C | T | 3 | a0001c0006t0007g0125a0002c0009t0007g0298a0007c0033t0007g0171 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3260-4340G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752904 | ||||||
| chr4:25752905
|
G | A | 2 | a0002c0002t0005g0187a0004c0007t0002g0168 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3260-4341C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752905 | ||||||
| chr4:25753031
|
T | C | 1 | a0018c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3260-4467A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753031 | ||||||
| chr4:25753069
|
C | G | 235 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(232): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.3259+4465G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753069 | ||||||
| chr4:25753107
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3259+4427G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753107 | ||||||
| chr4:25753124
|
G | A | 1 | a0010c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3259+4410C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753124 | ||||||
| chr4:25753133
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3259+4401C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753133 | ||||||
| chr4:25753176
|
A | G | 1 | a0004c0007t0002g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3259+4358T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753176 | ||||||
| chr4:25753231
|
A | C | 1 | a0010c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3259+4303T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753231 | ||||||
| chr4:25753419
|
T | C | 112 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(109): Show | 114 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.3259+4115A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753419 | ||||||
| chr4:25753517
|
C | G | 5 | a0001c0011t0003g0172a0002c0002t0005g0187a0002c0009t0003g0278others(2): Show | 5 | HG02572.hp1 HG03486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.3259+4017G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753517 | ||||||
| chr4:25753530
|
C | G | 1 | a0018c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3259+4004G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753530 | ||||||
| chr4:25753628
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3259+3906G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753628 | ||||||
| chr4:25753757
|
G | A | 2 | a0001c0011t0002g0055a0001c0011t0002g0101 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3259+3777C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753757 | ||||||
| chr4:25753758
|
T | C | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3259+3776A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753758 | ||||||
| chr4:25753961
|
G | A | 4 | a0001c0001t0010g0008a0001c0001t0010g0129a0001c0008t0012g0143others(1): Show | 4 | HG00741.hp1 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3259+3573C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753961 | ||||||
| chr4:25753975
|
C | G | 1 | a0001c0001t0001g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3259+3559G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753975 | ||||||
| chr4:25753984
|
C | CATAA | 51 | a0001c0001t0001g0012a0001c0001t0001g0077a0001c0001t0001g0193others(48): Show | 51 | HG00558.hp2 HG00741.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.3259+3546_3259+354 others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753984 | ||||||
| chr4:25753984
|
C | CATAAATA others(1): Show |
14 | a0001c0001t0001g0030a0001c0001t0001g0293a0001c0001t0003g0183others(11): Show | 16 | HG00438.hp1 HG01891.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3259+3542_3259+354 others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753984 | ||||||
| chr4:25753984
|
CATAA | C | 158 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.3259+3546_3259+354 others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753984 | ||||||
| chr4:25754004
|
A | C | 10 | a0001c0001t0001g0136a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG01109.hp1 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3259+3530T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754004 | ||||||
| chr4:25754173
|
A | C | 1 | a0001c0001t0002g0248 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3259+3361T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754173 | ||||||
| chr4:25754227
|
A | G | 279 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(276): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.3259+3307T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754227 | ||||||
| chr4:25754290
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3259+3244C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754290 | ||||||
| chr4:25754325
|
T | G | 2 | a0001c0011t0002g0055a0001c0011t0002g0101 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3259+3209A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754325 | ||||||
| chr4:25754351
|
CT | C | 107 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.3259+3182delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754351 | ||||||
| chr4:25754351
|
CTT | C | 15 | a0001c0001t0001g0287a0001c0001t0001g0293a0001c0001t0002g0140others(12): Show | 17 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.3259+3181_3259+318 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754351 | ||||||
| chr4:25754401
|
C | T | 112 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(109): Show | 114 | HG00609.hp1 HG00741.hp1 HG01074.hp2 others(111): Show |
intron_variant | MODIFIER | c.3259+3133G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754401 | ||||||
| chr4:25754416
|
T | G | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3259+3118A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754416 | ||||||
| chr4:25754420
|
C | T | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3259+3114G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754420 | ||||||
| chr4:25754566
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3259+2968C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754566 | ||||||
| chr4:25755141
|
T | C | 14 | a0001c0001t0001g0293a0001c0001t0002g0140a0001c0001t0002g0196others(11): Show | 16 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.3259+2393A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755141 | ||||||
| chr4:25755166
|
C | T | 1 | a0009c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3259+2368G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755166 | ||||||
| chr4:25755179
|
G | C | 5 | a0001c0001t0002g0155a0001c0001t0010g0008a0001c0001t0010g0129others(2): Show | 5 | HG00741.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3259+2355C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755179 | ||||||
| chr4:25755251
|
T | TTTTTA | 19 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0193others(16): Show | 19 | HG00438.hp1 HG00558.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.3259+2278_3259+228 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755251 | ||||||
| chr4:25755251
|
T | TTTTTATT others(3): Show |
2 | a0001c0001t0002g0052a0001c0001t0002g0106 | 2 | HG01358.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.3259+2273_3259+228 others(14): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755251 | ||||||
| chr4:25755251
|
T | TTTTTATT others(8): Show |
1 | a0001c0001t0002g0246 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3259+2268_3259+228 others(19): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755251 | ||||||
| chr4:25755251
|
TTTTTA | T | 109 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(106): Show | 111 | HG00609.hp1 HG00741.hp1 HG01074.hp2 others(108): Show |
intron_variant | MODIFIER | c.3259+2278_3259+228 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755251 | ||||||
| chr4:25755385
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3259+2149T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755385 | ||||||
| chr4:25755466
|
G | A | 7 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0081others(4): Show | 7 | HG02074.hp1 HG02083.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.3259+2068C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755466 | ||||||
| chr4:25755525
|
T | G | 86 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(83): Show | 88 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(85): Show |
intron_variant | MODIFIER | c.3259+2009A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755525 | ||||||
| chr4:25755677
|
G | A | 3 | a0007c0031t0020g0169a0013c0026t0013g0280a0018c0032t0019g0170 | 3 | HG03209.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3259+1857C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755677 | ||||||
| chr4:25755773
|
T | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0112a0001c0001t0001g0113others(1): Show | 4 | HG00140.hp1 HG00733.hp2 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.3259+1761A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755773 | ||||||
| chr4:25755817
|
T | C | 2 | a0001c0003t0002g0096a0001c0003t0002g0097 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3259+1717A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755817 | ||||||
| chr4:25755834
|
A | G | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3259+1700T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755834 | ||||||
| chr4:25755875
|
G | C | 4 | a0001c0001t0010g0008a0001c0001t0010g0129a0001c0008t0012g0143others(1): Show | 4 | HG00741.hp1 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3259+1659C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755875 | ||||||
| chr4:25756146
|
C | T | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3259+1388G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756146 | ||||||
| chr4:25756147
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3259+1387C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756147 | ||||||
| chr4:25756236
|
C | T | 3 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0264 | 3 | HG00738.hp2 HG01928.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.3259+1298G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756236 | ||||||
| chr4:25756237
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3259+1297C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756237 | ||||||
| chr4:25756452
|
G | A | 2 | a0001c0001t0010g0008a0001c0001t0010g0129 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3259+1082C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756452 | ||||||
| chr4:25756474
|
T | C | 1 | a0001c0001t0002g0275 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3259+1060A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756474 | ||||||
| chr4:25756654
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3259+880C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756654 | ||||||
| chr4:25756734
|
A | G | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3259+800T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756734 | ||||||
| chr4:25756797
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3259+737G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756797 | ||||||
| chr4:25756958
|
G | A | 279 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(276): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.3259+576C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756958 | ||||||
| chr4:25757033
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0016others(38): Show | 42 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.3259+501A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757033 | ||||||
| chr4:25757104
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3259+430G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757104 | ||||||
| chr4:25757291
|
A | C | 1 | a0001c0001t0001g0217 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3259+243T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757291 | ||||||
| chr4:25757318
|
A | G | 279 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(276): Show | 282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.3259+216T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757318 | ||||||
| chr4:25757334
|
C | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0231a0001c0001t0001g0271 | 3 | NA18939.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.3259+200G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757334 | ||||||
| chr4:25757342
|
G | A | 172 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(169): Show | 175 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.3259+192C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757342 | ||||||
| chr4:25757373
|
T | C | 70 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(67): Show | 70 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.3259+161A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757373 | ||||||
| chr4:25757455
|
AC | A | 87 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.3259+78delG | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757455 | ||||||
| chr4:25757457
|
C | A | 18 | a0001c0001t0001g0028a0001c0001t0001g0037a0001c0001t0001g0047others(15): Show | 18 | HG00438.hp2 HG00597.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.3259+77G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757457 | ||||||
| chr4:25757457
|
C | CA | 13 | a0001c0001t0002g0032a0001c0001t0002g0139a0001c0001t0002g0148others(10): Show | 13 | HG00738.hp1 HG00741.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3259+76dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757457 | ||||||
| chr4:25757457
|
CA | C | 85 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0042others(82): Show | 85 | HG00558.hp2 HG00609.hp1 HG01074.hp2 others(82): Show |
intron_variant | MODIFIER | c.3259+76delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757457 | ||||||
| chr4:25757457
|
CAA | C | 22 | a0001c0001t0002g0155a0001c0001t0002g0174a0001c0001t0002g0176others(19): Show | 22 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.3259+75_3259+76del others(2): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757457 | ||||||
| chr4:25757487
|
CT | C | 170 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(167): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.3259+46delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757487 | ||||||
| chr4:25757488
|
T | C | 69 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(66): Show | 69 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(66): Show |
intron_variant | MODIFIER | c.3259+46A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757488 | ||||||
| chr4:25757676
|
C | G | 44 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0084others(41): Show | 46 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.3186+12G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 22/23 | chr4 | 25757676 | ||||||
| chr4:25757850
|
A | T | 1 | a0001c0003t0002g0013 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3084-60T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25757850 | ||||||
| chr4:25757862
|
A | C | 4 | a0001c0001t0002g0126a0004c0007t0001g0164a0004c0007t0001g0165others(1): Show | 4 | HG02965.hp1 HG02970.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.3084-72T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25757862 | ||||||
| chr4:25758069
|
A | T | 128 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.3084-279T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758069 | ||||||
| chr4:25758153
|
G | A | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3084-363C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758153 | ||||||
| chr4:25758195
|
G | A | 3 | a0001c0001t0009g0124a0001c0001t0009g0285a0001c0003t0009g0027 | 3 | HG01891.hp1 HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3084-405C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758195 | ||||||
| chr4:25758361
|
C | T | 3 | a0001c0006t0007g0125a0002c0009t0007g0298a0007c0033t0007g0171 | 3 | HG02258.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3084-571G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758361 | ||||||
| chr4:25758388
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3083+553A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758388 | ||||||
| chr4:25758559
|
C | T | 10 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0016others(7): Show | 11 | HG00733.hp1 HG00738.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.3083+382G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758559 | ||||||
| chr4:25758674
|
CTT | C | 21 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0084others(18): Show | 21 | HG00558.hp2 HG00741.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.3083+265_3083+266d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758674 | ||||||
| chr4:25758678
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3083+263A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758678 | ||||||
| chr4:25758761
|
G | T | 20 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0084others(17): Show | 20 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.3083+180C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758761 | ||||||
| chr4:25758859
|
G | T | 1 | a0001c0001t0017g0090 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3083+82C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758859 | ||||||
| chr4:25758876
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3083+65G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758876 | ||||||
| chr4:25759071
|
A | G | 70 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(67): Show | 70 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(67): Show |
splice_region_variant&intron_variant | LOW | c.2956-3T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759071 | ||||||
| chr4:25759158
|
C | G | 1 | a0001c0017t0002g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2956-90G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759158 | ||||||
| chr4:25759163
|
AT | A | 9 | a0001c0006t0002g0154a0001c0006t0004g0092a0001c0006t0004g0132others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2956-96delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759163 | ||||||
| chr4:25759206
|
T | C | 115 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(112): Show | 116 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.2956-138A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759206 | ||||||
| chr4:25759236
|
C | G | 20 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0084others(17): Show | 20 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.2956-168G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759236 | ||||||
| chr4:25759252
|
CA | C | 21 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0016others(18): Show | 22 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2956-185delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759252 | ||||||
| chr4:25759263
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0015a0001c0001t0002g0016others(39): Show | 43 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2956-195C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759263 | ||||||
| chr4:25759281
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2956-213G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759281 | ||||||
| chr4:25759322
|
G | A | 22 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0084others(19): Show | 22 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2956-254C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759322 | ||||||
| chr4:25759696
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2956-628G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759696 | ||||||
| chr4:25759783
|
C | T | 1 | a0001c0010t0022g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2956-715G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759783 | ||||||
| chr4:25759784
|
A | G | 137 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(134): Show | 138 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.2956-716T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759784 | ||||||
| chr4:25759797
|
C | T | 2 | a0001c0003t0002g0096a0001c0003t0002g0097 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2956-729G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759797 | ||||||
| chr4:25759798
|
A | G | 265 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(262): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.2956-730T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759798 | ||||||
| chr4:25759877
|
G | C | 1 | a0001c0001t0001g0012 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2956-809C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759877 | ||||||
| chr4:25760099
|
T | C | 1 | a0004c0007t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2956-1031A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760099 | ||||||
| chr4:25760157
|
G | A | 2 | a0002c0002t0005g0187a0012c0016t0002g0141 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2956-1089C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760157 | ||||||
| chr4:25760241
|
C | T | 3 | a0001c0001t0003g0149a0001c0010t0022g0307a0002c0005t0003g0122 | 3 | HG03041.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2956-1173G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760241 | ||||||
| chr4:25760268
|
T | C | 20 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0084others(17): Show | 20 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.2956-1200A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760268 | ||||||
| chr4:25760313
|
G | A | 3 | a0007c0031t0020g0169a0013c0026t0013g0280a0018c0032t0019g0170 | 3 | HG03209.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2956-1245C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760313 | ||||||
| chr4:25760695
|
A | G | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2956-1627T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760695 | ||||||
| chr4:25760760
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2956-1692C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760760 | ||||||
| chr4:25761298
|
G | A | 114 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(111): Show | 115 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.2956-2230C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761298 | ||||||
| chr4:25761301
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2956-2233C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761301 | ||||||
| chr4:25761348
|
G | C | 2 | a0001c0001t0010g0008a0001c0001t0010g0129 | 2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2956-2280C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761348 | ||||||
| chr4:25761348
|
G | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0218 | 2 | NA18993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2956-2280C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761348 | ||||||
| chr4:25761420
|
T | C | 265 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(262): Show | 266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.2956-2352A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761420 | ||||||
| chr4:25761421
|
G | A | 2 | a0001c0001t0002g0295a0010c0037t0003g0304 | 2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2956-2353C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761421 | ||||||
| chr4:25761447
|
C | T | 2 | a0001c0008t0012g0143a0008c0038t0012g0305 | 2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2956-2379G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761447 | ||||||
| chr4:25761623
|
A | G | 3 | a0001c0001t0002g0295a0002c0002t0005g0187a0010c0037t0003g0304 | 3 | HG02145.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2956-2555T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761623 | ||||||
| chr4:25761669
|
C | G | 1 | a0001c0001t0002g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2956-2601G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761669 | ||||||
| chr4:25761770
|
A | G | 1 | a0002c0009t0004g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2956-2702T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761770 | ||||||
| chr4:25762138
|
G | T | 1 | a0001c0001t0002g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2956-3070C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762138 | ||||||
| chr4:25762431
|
C | G | 266 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(263): Show | 267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.2955+2895G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762431 | ||||||
| chr4:25762695
|
C | T | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2955+2631G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762695 | ||||||
| chr4:25762709
|
G | T | 115 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(112): Show | 116 | HG00558.hp1 HG00609.hp1 HG00642.hp2 others(113): Show |
intron_variant | MODIFIER | c.2955+2617C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762709 | ||||||
| chr4:25762803
|
C | G | 21 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0084others(18): Show | 21 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2955+2523G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762803 | ||||||
| chr4:25762821
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2955+2505G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762821 | ||||||
| chr4:25762877
|
G | A | 3 | a0001c0001t0002g0174a0001c0001t0002g0176a0001c0001t0002g0260 | 3 | HG03017.hp1 HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2955+2449C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762877 | ||||||
| chr4:25762953
|
C | T | 2 | a0005c0019t0002g0010a0012c0016t0002g0141 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2955+2373G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762953 | ||||||
| chr4:25762974
|
C | CA | 91 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(88): Show | 91 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.2955+2351dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762974 | ||||||
| chr4:25762974
|
CAA | C | 20 | a0001c0001t0001g0030a0001c0001t0001g0077a0001c0001t0001g0084others(17): Show | 20 | HG00438.hp1 HG00558.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.2955+2350_2955+235 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762974 | ||||||
| chr4:25763037
|
G | C | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2955+2289C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763037 | ||||||
| chr4:25763185
|
G | GA | 134 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(131): Show | 137 | HG00558.hp1 HG00609.hp1 HG00642.hp2 others(134): Show |
intron_variant | MODIFIER | c.2955+2140dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763185 | ||||||
| chr4:25763231
|
C | G | 1 | a0001c0001t0002g0003 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2955+2095G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763231 | ||||||
| chr4:25763293
|
T | C | 3 | a0001c0001t0010g0008a0001c0001t0010g0129a0012c0016t0002g0141 | 3 | HG00741.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2955+2033A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763293 | ||||||
| chr4:25763376
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2955+1950C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763376 | ||||||
| chr4:25763690
|
C | A | 236 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0021others(233): Show | 239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2955+1636G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763690 | ||||||
| chr4:25763705
|
G | A | 129 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(126): Show | 130 | HG00558.hp1 HG00609.hp1 HG00642.hp2 others(127): Show |
intron_variant | MODIFIER | c.2955+1621C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763705 | ||||||
| chr4:25763892
|
G | C | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2955+1434C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763892 | ||||||
| chr4:25763905
|
G | A | 251 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0021others(248): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.2955+1421C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763905 | ||||||
| chr4:25763911
|
G | T | 1 | a0001c0001t0002g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2955+1415C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763911 | ||||||
| chr4:25763942
|
A | G | 8 | a0001c0006t0002g0154a0001c0006t0004g0092a0001c0006t0004g0132others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2955+1384T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763942 | ||||||
| chr4:25763996
|
A | G | 5 | a0001c0001t0003g0149a0001c0010t0022g0307a0001c0011t0003g0172others(2): Show | 5 | HG02572.hp1 HG03041.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+1330T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763996 | ||||||
| chr4:25764021
|
C | A | 8 | a0001c0006t0002g0154a0001c0006t0004g0092a0001c0006t0004g0132others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2955+1305G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764021 | ||||||
| chr4:25764064
|
C | T | 1 | a0001c0001t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2955+1262G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764064 | ||||||
| chr4:25764065
|
G | A | 5 | a0001c0001t0005g0300a0001c0001t0009g0124a0001c0001t0009g0285others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2955+1261C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764065 | ||||||
| chr4:25764079
|
G | T | 1 | a0001c0001t0001g0043 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2955+1247C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764079 | ||||||
| chr4:25764087
|
C | T | 3 | a0001c0001t0010g0008a0001c0001t0010g0129a0012c0016t0002g0141 | 3 | HG00741.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2955+1239G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764087 | ||||||
| chr4:25764088
|
G | A | 49 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0235others(46): Show | 50 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.2955+1238C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764088 | ||||||
| chr4:25764190
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2955+1136C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764190 | ||||||
| chr4:25764262
|
A | T | 72 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(69): Show | 72 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.2955+1064T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764262 | ||||||
| chr4:25764357
|
G | A | 1 | a0001c0001t0003g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2955+969C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764357 | ||||||
| chr4:25764412
|
G | A | 1 | a0001c0001t0002g0002 | 2 | HG00733.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2955+914C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764412 | ||||||
| chr4:25764523
|
G | T | 2 | a0005c0019t0002g0010a0016c0020t0002g0011 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2955+803C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764523 | ||||||
| chr4:25764562
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2955+764C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764562 | ||||||
| chr4:25764603
|
T | C | 1 | a0001c0001t0002g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2955+723A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764603 | ||||||
| chr4:25765029
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2955+297G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765029 | ||||||
| chr4:25765037
|
C | T | 78 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(75): Show | 78 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.2955+289G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765037 | ||||||
| chr4:25765063
|
C | T | 6 | a0001c0006t0007g0125a0001c0011t0002g0055a0001c0011t0002g0101others(3): Show | 6 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2955+263G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765063 | ||||||
| chr4:25765140
|
G | A | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2955+186C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765140 | ||||||
| chr4:25765269
|
C | A | 13 | a0001c0001t0001g0293a0001c0001t0002g0140a0001c0001t0005g0300others(10): Show | 15 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2955+57G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765269 | ||||||
| chr4:25765289
|
C | G | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2955+37G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765289 | ||||||
| chr4:25765442
|
G | A | 3 | a0001c0001t0002g0295a0002c0018t0002g0158a0010c0037t0003g0304 | 3 | HG02145.hp2 HG03225.hp1 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.2846-7C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765442 | ||||||
| chr4:25765497
|
T | G | 4 | a0001c0001t0002g0128a0001c0001t0002g0134a0001c0001t0002g0151others(1): Show | 4 | HG02630.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2846-62A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765497 | ||||||
| chr4:25765511
|
A | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0030others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.2846-76T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765511 | ||||||
| chr4:25765561
|
G | A | 205 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0021others(202): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.2846-126C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765561 | ||||||
| chr4:25765752
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2846-317G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765752 | ||||||
| chr4:25766058
|
G | T | 6 | a0001c0006t0007g0125a0001c0011t0002g0055a0001c0011t0002g0101others(3): Show | 6 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2846-623C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766058 | ||||||
| chr4:25766154
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-719T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766154 | ||||||
| chr4:25766157
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-722C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766157 | ||||||
| chr4:25766158
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-723C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766158 | ||||||
| chr4:25766159
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-724G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766159 | ||||||
| chr4:25766160
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-725A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766160 | ||||||
| chr4:25766282
|
A | G | 1 | a0006c0012t0002g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2846-847T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766282 | ||||||
| chr4:25766344
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2846-909C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766344 | ||||||
| chr4:25766389
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2846-954C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766389 | ||||||
| chr4:25766439
|
C | CA | 8 | a0001c0001t0001g0145a0001c0001t0001g0245a0001c0001t0002g0178others(5): Show | 8 | HG01515.hp2 HG02055.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2846-1005dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766439 | ||||||
| chr4:25766439
|
CA | C | 80 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(77): Show | 80 | HG00609.hp1 HG01070.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.2846-1005delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766439 | ||||||
| chr4:25766439
|
CAA | C | 12 | a0001c0001t0001g0215a0001c0001t0001g0293a0001c0001t0002g0140others(9): Show | 14 | HG00741.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2846-1006_2846-100 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766439 | ||||||
| chr4:25766459
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2846-1024C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766459 | ||||||
| chr4:25766500
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2845+1025C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766500 | ||||||
| chr4:25766508
|
T | C | 8 | a0001c0001t0001g0293a0001c0001t0002g0140a0001c0001t0006g0150others(5): Show | 10 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2845+1017A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766508 | ||||||
| chr4:25766599
|
G | C | 6 | a0001c0006t0007g0125a0001c0011t0002g0055a0001c0011t0002g0101others(3): Show | 6 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2845+926C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766599 | ||||||
| chr4:25766627
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2845+898G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766627 | ||||||
| chr4:25766674
|
A | G | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2845+851T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766674 | ||||||
| chr4:25766855
|
C | T | 1 | a0001c0001t0002g0105 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2845+670G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766855 | ||||||
| chr4:25766867
|
G | T | 1 | a0001c0001t0003g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2845+658C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766867 | ||||||
| chr4:25766868
|
A | C | 1 | a0001c0001t0003g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2845+657T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766868 | ||||||
| chr4:25766919
|
G | A | 1 | a0016c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2845+606C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766919 | ||||||
| chr4:25766957
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2845+568G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766957 | ||||||
| chr4:25767002
|
A | T | 1 | a0001c0001t0002g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2845+523T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767002 | ||||||
| chr4:25767030
|
G | A | 3 | a0001c0001t0002g0295a0002c0018t0002g0158a0010c0037t0003g0304 | 3 | HG02145.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2845+495C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767030 | ||||||
| chr4:25767155
|
G | A | 92 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0030others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.2845+370C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767155 | ||||||
| chr4:25767160
|
C | G | 1 | a0002c0018t0002g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2845+365G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767160 | ||||||
| chr4:25767417
|
C | A | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2845+108G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767417 | ||||||
| chr4:25767419
|
A | T | 3 | a0001c0001t0002g0295a0002c0018t0002g0158a0010c0037t0003g0304 | 3 | HG02145.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2845+106T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767419 | ||||||
| chr4:25767507
|
C | G | 71 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(68): Show | 71 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.2845+18G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767507 | ||||||
| chr4:25767508
|
C | G | 71 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(68): Show | 71 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.2845+17G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767508 | ||||||
| chr4:25767513
|
T | C | 161 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0030others(158): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2845+12A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767513 | ||||||
| chr4:25767614
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG01106.hp1 | splice_region_variant&intron_variant | LOW | c.2761-5C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 18/23 | chr4 | 25767614 | ||||||
| chr4:25767622
|
G | A | 3 | a0001c0001t0010g0008a0001c0001t0010g0129a0012c0016t0002g0141 | 3 | HG00741.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2761-13C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 18/23 | chr4 | 25767622 | ||||||
| chr4:25767697
|
T | C | 71 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(68): Show | 71 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.2760+43A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 18/23 | chr4 | 25767697 | ||||||
| chr4:25767705
|
A | G | 71 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(68): Show | 71 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.2760+35T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 18/23 | chr4 | 25767705 | ||||||
| chr4:25767838
|
T | C | 5 | a0001c0006t0007g0125a0001c0011t0002g0055a0001c0011t0002g0101others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2670-8A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25767838 | ||||||
| chr4:25767964
|
T | A | 2 | a0001c0001t0001g0047a0001c0001t0002g0196 | 2 | HG02055.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2670-134A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25767964 | ||||||
| chr4:25768011
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2670-181C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768011 | ||||||
| chr4:25768254
|
C | T | 5 | a0001c0006t0007g0125a0001c0011t0002g0055a0001c0011t0002g0101others(2): Show | 5 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2670-424G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768254 | ||||||
| chr4:25768349
|
C | T | 107 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0040others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.2670-519G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768349 | ||||||
| chr4:25768460
|
G | A | 1 | a0001c0001t0003g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2670-630C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768460 | ||||||
| chr4:25768506
|
C | T | 1 | a0001c0001t0002g0302 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2670-676G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768506 | ||||||
| chr4:25768612
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2670-782C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768612 | ||||||
| chr4:25768763
|
G | A | 11 | a0001c0006t0002g0154a0001c0006t0004g0092a0001c0006t0004g0132others(8): Show | 11 | HG02280.hp2 HG02451.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2670-933C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768763 | ||||||
| chr4:25768830
|
T | C | 2 | a0001c0008t0001g0162a0002c0002t0001g0279 | 2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2670-1000A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768830 | ||||||
| chr4:25768844
|
T | C | 1 | a0002c0018t0002g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2670-1014A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768844 | ||||||
| chr4:25768902
|
G | C | 70 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(67): Show | 70 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.2670-1072C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768902 | ||||||
| chr4:25769028
|
A | AT | 240 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0021others(237): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.2670-1199dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769028 | ||||||
| chr4:25769266
|
A | G | 5 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0291others(2): Show | 5 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670-1436T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769266 | ||||||
| chr4:25769493
|
G | A | 255 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0021others(252): Show | 257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.2670-1663C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769493 | ||||||
| chr4:25769514
|
T | G | 6 | a0001c0001t0003g0149a0001c0001t0003g0286a0001c0010t0022g0307others(3): Show | 6 | HG02886.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2670-1684A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769514 | ||||||
| chr4:25769698
|
G | A | 2 | a0001c0001t0002g0176a0001c0001t0016g0091 | 2 | HG03669.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2670-1868C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769698 | ||||||
| chr4:25769738
|
T | C | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2670-1908A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769738 | ||||||
| chr4:25769759
|
C | T | 9 | a0001c0001t0001g0075a0001c0001t0001g0080a0001c0001t0001g0081others(6): Show | 9 | HG02074.hp1 HG02083.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.2670-1929G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769759 | ||||||
| chr4:25769851
|
C | A | 2 | a0002c0005t0001g0156a0002c0005t0001g0157 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2670-2021G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769851 | ||||||
| chr4:25769855
|
T | G | 2 | a0002c0005t0001g0156a0002c0005t0001g0157 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2670-2025A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769855 | ||||||
| chr4:25769885
|
T | C | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2670-2055A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769885 | ||||||
| chr4:25769978
|
A | T | 3 | a0001c0001t0006g0150a0002c0002t0006g0268a0002c0005t0006g0001 | 5 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670-2148T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769978 | ||||||
| chr4:25770023
|
G | A | 48 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0028others(45): Show | 48 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.2670-2193C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770023 | ||||||
| chr4:25770168
|
G | C | 2 | a0001c0001t0009g0285a0001c0003t0009g0027 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2670-2338C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770168 | ||||||
| chr4:25770169
|
C | T | 90 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(87): Show | 91 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.2670-2339G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770169 | ||||||
| chr4:25770257
|
T | C | 1 | a0002c0002t0002g0133 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2670-2427A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770257 | ||||||
| chr4:25770274
|
T | C | 2 | a0001c0001t0002g0259a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2670-2444A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770274 | ||||||
| chr4:25770336
|
C | A | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2670-2506G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770336 | ||||||
| chr4:25770351
|
C | T | 177 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(174): Show | 180 | HG00140.hp2 HG00558.hp1 HG00642.hp1 others(177): Show |
intron_variant | MODIFIER | c.2670-2521G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770351 | ||||||
| chr4:25770461
|
C | T | 24 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0139others(21): Show | 24 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.2670-2631G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770461 | ||||||
| chr4:25770575
|
G | A | 119 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0037others(116): Show | 119 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.2670-2745C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770575 | ||||||
| chr4:25770612
|
C | T | 2 | a0001c0008t0007g0161a0007c0031t0020g0169 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2670-2782G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770612 | ||||||
| chr4:25770671
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2670-2841G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770671 | ||||||
| chr4:25770739
|
C | CA | 18 | a0001c0001t0001g0293a0001c0001t0003g0149a0001c0001t0003g0265others(15): Show | 20 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.2670-2910dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770739 | ||||||
| chr4:25770739
|
CA | C | 13 | a0001c0001t0001g0184a0001c0001t0001g0225a0001c0001t0001g0235others(10): Show | 13 | HG00642.hp2 HG01106.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2670-2910delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770739 | ||||||
| chr4:25770739
|
CAA | C | 179 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0030others(176): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2670-2911_2670-291 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770739 | ||||||
| chr4:25770739
|
CAAA | C | 17 | a0001c0001t0002g0031a0001c0001t0002g0139a0001c0001t0002g0302others(14): Show | 17 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2670-2912_2670-291 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770739 | ||||||
| chr4:25770760
|
A | G | 1 | a0001c0001t0003g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2670-2930T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770760 | ||||||
| chr4:25770837
|
G | C | 227 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0030others(224): Show | 230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.2670-3007C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770837 | ||||||
| chr4:25770855
|
T | C | 206 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0030others(203): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.2670-3025A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770855 | ||||||
| chr4:25770874
|
G | A | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2670-3044C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770874 | ||||||
| chr4:25771167
|
C | A | 1 | a0018c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2670-3337G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771167 | ||||||
| chr4:25771199
|
C | A | 1 | a0014c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2670-3369G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771199 | ||||||
| chr4:25771216
|
T | C | 2 | a0001c0001t0002g0196a0001c0034t0002g0137 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2670-3386A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771216 | ||||||
| chr4:25771344
|
G | A | 2 | a0001c0008t0007g0161a0007c0031t0020g0169 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2670-3514C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771344 | ||||||
| chr4:25771449
|
C | A | 204 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0030others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.2670-3619G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771449 | ||||||
| chr4:25771522
|
C | T | 1 | a0001c0001t0002g0002 | 2 | HG00733.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2670-3692G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771522 | ||||||
| chr4:25771575
|
A | C | 97 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0037others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.2670-3745T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771575 | ||||||
| chr4:25771743
|
A | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2670-3913T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771743 | ||||||
| chr4:25771828
|
C | T | 95 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0037others(92): Show | 95 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2670-3998G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771828 | ||||||
| chr4:25771838
|
C | T | 1 | a0001c0008t0012g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2670-4008G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771838 | ||||||
| chr4:25771888
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0095a0001c0001t0002g0147others(1): Show | 4 | HG02040.hp2 NA18993.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2670-4058C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771888 | ||||||
| chr4:25772356
|
G | A | 2 | a0001c0001t0002g0242a0001c0001t0003g0086 | 2 | HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2669+3921C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25772356 | ||||||
| chr4:25772641
|
G | A | 11 | a0001c0001t0001g0136a0001c0001t0001g0296a0001c0001t0002g0139others(8): Show | 11 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2669+3636C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25772641 | ||||||
| chr4:25772811
|
T | A | 18 | a0001c0001t0001g0235a0001c0001t0001g0256a0001c0001t0002g0002others(15): Show | 19 | HG00642.hp2 HG00733.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.2669+3466A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25772811 | ||||||
| chr4:25772922
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0001g0252 | 2 | NA18970.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2669+3355G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25772922 | ||||||
| chr4:25773085
|
C | T | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2669+3192G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773085 | ||||||
| chr4:25773279
|
A | G | 1 | a0003c0004t0001g0146 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2669+2998T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773279 | ||||||
| chr4:25773382
|
G | T | 1 | a0001c0001t0002g0003 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2669+2895C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773382 | ||||||
| chr4:25773412
|
T | C | 42 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0056others(39): Show | 42 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.2669+2865A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773412 | ||||||
| chr4:25773602
|
A | T | 170 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0030others(167): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.2669+2675T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773602 | ||||||
| chr4:25773628
|
C | T | 20 | a0001c0001t0001g0136a0001c0001t0001g0296a0001c0001t0002g0126others(17): Show | 20 | HG01192.hp2 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2669+2649G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773628 | ||||||
| chr4:25773666
|
A | G | 112 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0035others(109): Show | 115 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.2669+2611T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773666 | ||||||
| chr4:25773718
|
C | G | 5 | a0001c0001t0002g0302a0002c0002t0002g0277a0002c0002t0002g0281others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2669+2559G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773718 | ||||||
| chr4:25773896
|
C | T | 2 | a0001c0010t0002g0173a0001c0010t0022g0307 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2669+2381G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773896 | ||||||
| chr4:25773985
|
A | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | NA18942.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2669+2292T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773985 | ||||||
| chr4:25773996
|
G | A | 56 | a0001c0001t0001g0117a0001c0001t0001g0258a0001c0001t0002g0014others(53): Show | 56 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.2669+2281C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773996 | ||||||
| chr4:25774169
|
T | G | 14 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0082others(11): Show | 14 | HG00673.hp2 HG02027.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.2669+2108A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774169 | ||||||
| chr4:25774208
|
C | T | 2 | a0001c0010t0002g0173a0001c0010t0022g0307 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2669+2069G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774208 | ||||||
| chr4:25774394
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2669+1883A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774394 | ||||||
| chr4:25774719
|
G | A | 225 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(222): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2669+1558C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774719 | ||||||
| chr4:25774919
|
C | T | 2 | a0001c0010t0002g0173a0001c0010t0022g0307 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2669+1358G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774919 | ||||||
| chr4:25775032
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2669+1245C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775032 | ||||||
| chr4:25775060
|
G | C | 1 | a0001c0001t0002g0062 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2669+1217C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775060 | ||||||
| chr4:25775203
|
T | A | 2 | a0001c0001t0001g0296a0001c0008t0007g0161 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2669+1074A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775203 | ||||||
| chr4:25775441
|
T | G | 3 | a0001c0001t0002g0242a0001c0001t0003g0086a0001c0001t0009g0285 | 3 | HG01891.hp1 HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2669+836A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775441 | ||||||
| chr4:25775460
|
G | T | 166 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(163): Show | 169 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2669+817C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775460 | ||||||
| chr4:25775527
|
A | G | 222 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(219): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.2669+750T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775527 | ||||||
| chr4:25775655
|
G | A | 17 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0056others(14): Show | 17 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.2669+622C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775655 | ||||||
| chr4:25775876
|
C | T | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2669+401G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775876 | ||||||
| chr4:25775905
|
C | A | 1 | a0001c0001t0002g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2669+372G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775905 | ||||||
| chr4:25776134
|
G | C | 2 | a0001c0001t0001g0120a0001c0027t0001g0197 | 2 | HG00733.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.2669+143C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25776134 | ||||||
| chr4:25776180
|
C | A | 8 | a0001c0001t0002g0302a0001c0001t0008g0114a0001c0001t0008g0290others(5): Show | 8 | HG01074.hp1 HG01257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2669+97G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25776180 | ||||||
| chr4:25776645
|
C | T | 4 | a0001c0001t0001g0040a0001c0001t0001g0249a0001c0001t0001g0271others(1): Show | 4 | NA18939.hp1 NA18944.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.2586-285G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776645 | ||||||
| chr4:25776650
|
A | G | 1 | a0003c0004t0001g0146 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2586-290T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776650 | ||||||
| chr4:25776716
|
T | C | 225 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(222): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2586-356A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776716 | ||||||
| chr4:25776837
|
AT | A | 53 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(50): Show | 53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2586-478delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776837 | ||||||
| chr4:25776886
|
A | T | 3 | a0001c0001t0002g0242a0001c0001t0003g0086a0001c0001t0009g0285 | 3 | HG01891.hp1 HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2586-526T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776886 | ||||||
| chr4:25776902
|
A | C | 170 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(167): Show | 173 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(170): Show |
intron_variant | MODIFIER | c.2586-542T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776902 | ||||||
| chr4:25776984
|
G | T | 1 | a0001c0001t0002g0014 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2586-624C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776984 | ||||||
| chr4:25777029
|
C | A | 3 | a0001c0001t0002g0242a0001c0001t0003g0086a0001c0001t0009g0285 | 3 | HG01891.hp1 HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2586-669G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777029 | ||||||
| chr4:25777045
|
A | G | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2586-685T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777045 | ||||||
| chr4:25777135
|
A | G | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2586-775T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777135 | ||||||
| chr4:25777191
|
A | C | 1 | a0001c0001t0001g0215 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2586-831T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777191 | ||||||
| chr4:25777292
|
C | T | 1 | a0003c0004t0001g0146 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2586-932G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777292 | ||||||
| chr4:25777325
|
T | C | 53 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(50): Show | 53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2586-965A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777325 | ||||||
| chr4:25777361
|
A | G | 167 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(164): Show | 170 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.2586-1001T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777361 | ||||||
| chr4:25777440
|
G | T | 167 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(164): Show | 170 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.2586-1080C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777440 | ||||||
| chr4:25777538
|
G | A | 308 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.2586-1178C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777538 | ||||||
| chr4:25777794
|
G | T | 2 | a0001c0001t0002g0208a0001c0001t0002g0248 | 2 | HG01169.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2585+1282C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777794 | ||||||
| chr4:25777800
|
A | G | 4 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0060others(1): Show | 4 | NA18955.hp2 NA18973.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.2585+1276T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777800 | ||||||
| chr4:25777827
|
C | T | 12 | a0001c0001t0002g0302a0001c0001t0008g0114a0001c0001t0008g0290others(9): Show | 12 | HG01074.hp1 HG01257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2585+1249G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777827 | ||||||
| chr4:25777914
|
T | C | 1 | a0010c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2585+1162A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777914 | ||||||
| chr4:25778063
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2585+1013C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778063 | ||||||
| chr4:25778155
|
C | T | 12 | a0001c0001t0002g0302a0001c0001t0008g0114a0001c0001t0008g0290others(9): Show | 12 | HG01074.hp1 HG01257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2585+921G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778155 | ||||||
| chr4:25778363
|
A | G | 167 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(164): Show | 170 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.2585+713T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778363 | ||||||
| chr4:25778465
|
A | T | 2 | a0001c0001t0002g0105a0001c0001t0002g0180 | 2 | HG02135.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2585+611T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778465 | ||||||
| chr4:25778525
|
T | C | 225 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(222): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2585+551A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778525 | ||||||
| chr4:25778925
|
G | T | 167 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(164): Show | 170 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.2585+151C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778925 | ||||||
| chr4:25778977
|
C | T | 167 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(164): Show | 170 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.2585+99G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778977 | ||||||
| chr4:25779269
|
A | G | 225 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(222): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2458-66T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25779269 | ||||||
| chr4:25779389
|
C | G | 1 | a0001c0001t0003g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2458-186G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25779389 | ||||||
| chr4:25779933
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2458-730A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25779933 | ||||||
| chr4:25779938
|
C | T | 1 | a0009c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2458-735G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25779938 | ||||||
| chr4:25780090
|
T | A | 2 | a0002c0018t0002g0158a0007c0031t0020g0169 | 2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2458-887A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780090 | ||||||
| chr4:25780139
|
G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2458-936C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780139 | ||||||
| chr4:25780161
|
C | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0057a0001c0001t0001g0059others(2): Show | 5 | HG01074.hp2 HG01257.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.2458-958G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780161 | ||||||
| chr4:25780290
|
C | G | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2458-1087G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780290 | ||||||
| chr4:25780541
|
C | T | 5 | a0001c0001t0002g0242a0001c0001t0003g0086a0001c0001t0009g0285others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2458-1338G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780541 | ||||||
| chr4:25780824
|
TTA | T | 167 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(164): Show | 170 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.2457+1416_2457+141 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780824 | ||||||
| chr4:25780886
|
C | T | 2 | a0001c0001t0002g0242a0001c0001t0003g0086 | 2 | HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2457+1356G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780886 | ||||||
| chr4:25780920
|
G | A | 2 | a0001c0010t0002g0173a0001c0010t0022g0307 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2457+1322C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780920 | ||||||
| chr4:25780959
|
G | C | 1 | a0001c0001t0018g0233 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2457+1283C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780959 | ||||||
| chr4:25780969
|
G | C | 167 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(164): Show | 170 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.2457+1273C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780969 | ||||||
| chr4:25781213
|
G | A | 53 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(50): Show | 53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2457+1029C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781213 | ||||||
| chr4:25781252
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2457+990T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781252 | ||||||
| chr4:25781366
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2457+876T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781366 | ||||||
| chr4:25781506
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2457+736A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781506 | ||||||
| chr4:25781543
|
C | T | 2 | a0005c0019t0002g0010a0016c0020t0002g0011 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2457+699G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781543 | ||||||
| chr4:25781676
|
C | T | 1 | a0003c0004t0001g0210 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2457+566G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781676 | ||||||
| chr4:25781836
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2457+406A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781836 | ||||||
| chr4:25781859
|
C | A | 2 | a0001c0001t0008g0114a0001c0001t0008g0290 | 2 | HG01074.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.2457+383G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781859 | ||||||
| chr4:25781882
|
T | C | 54 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(51): Show | 54 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.2457+360A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781882 | ||||||
| chr4:25782110
|
C | T | 1 | a0005c0021t0003g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2457+132G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25782110 | ||||||
| chr4:25782178
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2457+64A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25782178 | ||||||
| chr4:25782450
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2281-32A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782450 | ||||||
| chr4:25782470
|
A | C | 6 | a0001c0001t0001g0100a0001c0001t0002g0003a0001c0001t0002g0032others(3): Show | 6 | HG02683.hp2 HG03654.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.2281-52T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782470 | ||||||
| chr4:25782495
|
G | A | 12 | a0001c0001t0002g0302a0001c0001t0008g0114a0001c0001t0008g0290others(9): Show | 12 | HG01074.hp1 HG01257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2281-77C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782495 | ||||||
| chr4:25782698
|
C | T | 226 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(223): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2281-280G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782698 | ||||||
| chr4:25782715
|
C | T | 1 | a0001c0001t0002g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2281-297G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782715 | ||||||
| chr4:25782932
|
C | G | 129 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(126): Show | 132 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(129): Show |
intron_variant | MODIFIER | c.2281-514G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782932 | ||||||
| chr4:25782935
|
T | G | 226 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(223): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2281-517A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782935 | ||||||
| chr4:25783110
|
A | G | 109 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(106): Show | 112 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(109): Show |
intron_variant | MODIFIER | c.2281-692T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783110 | ||||||
| chr4:25783204
|
C | T | 55 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(52): Show | 55 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.2281-786G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783204 | ||||||
| chr4:25783357
|
A | C | 55 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(52): Show | 55 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.2280+871T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783357 | ||||||
| chr4:25783501
|
A | G | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2280+727T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783501 | ||||||
| chr4:25783539
|
C | A | 53 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(50): Show | 53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2280+689G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783539 | ||||||
| chr4:25783596
|
G | A | 2 | a0001c0001t0010g0008a0002c0002t0005g0187 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2280+632C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783596 | ||||||
| chr4:25783630
|
T | G | 2 | a0001c0001t0010g0008a0002c0002t0005g0187 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2280+598A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783630 | ||||||
| chr4:25783693
|
T | C | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2280+535A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783693 | ||||||
| chr4:25783824
|
C | A | 53 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(50): Show | 53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2280+404G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783824 | ||||||
| chr4:25783966
|
T | C | 1 | a0001c0001t0002g0250 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2280+262A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783966 | ||||||
| chr4:25784102
|
G | A | 2 | a0001c0001t0010g0008a0002c0002t0005g0187 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2280+126C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25784102 | ||||||
| chr4:25784315
|
T | C | 1 | a0010c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2218-25A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784315 | ||||||
| chr4:25784322
|
G | T | 1 | a0001c0001t0002g0242 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2218-32C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784322 | ||||||
| chr4:25784425
|
T | G | 9 | a0001c0001t0002g0139a0001c0001t0009g0124a0001c0006t0007g0125others(6): Show | 9 | HG02145.hp1 HG02965.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2218-135A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784425 | ||||||
| chr4:25784470
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2218-180G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784470 | ||||||
| chr4:25784796
|
T | C | 229 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(226): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.2218-506A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784796 | ||||||
| chr4:25785072
|
T | C | 2 | a0005c0021t0003g0283a0005c0022t0004g0284 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2218-782A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785072 | ||||||
| chr4:25785274
|
G | A | 2 | a0005c0019t0002g0010a0016c0020t0002g0011 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2218-984C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785274 | ||||||
| chr4:25785512
|
T | G | 15 | a0001c0001t0002g0126a0001c0001t0002g0139a0001c0001t0004g0123others(12): Show | 15 | HG01192.hp2 HG02145.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.2218-1222A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785512 | ||||||
| chr4:25785723
|
A | C | 6 | a0001c0001t0002g0242a0001c0001t0003g0086a0001c0001t0008g0114others(3): Show | 6 | HG01074.hp1 HG01257.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.2218-1433T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785723 | ||||||
| chr4:25785723
|
A | G | 214 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(211): Show | 217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.2218-1433T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785723 | ||||||
| chr4:25785780
|
T | C | 1 | a0010c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2218-1490A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785780 | ||||||
| chr4:25785903
|
T | A | 1 | a0001c0001t0002g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2218-1613A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785903 | ||||||
| chr4:25786204
|
T | C | 1 | a0014c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2218-1914A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786204 | ||||||
| chr4:25786216
|
A | G | 202 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.2218-1926T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786216 | ||||||
| chr4:25786265
|
C | T | 5 | a0001c0001t0002g0302a0002c0002t0002g0277a0002c0002t0002g0281others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2217+1959G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786265 | ||||||
| chr4:25786328
|
G | A | 1 | a0001c0010t0002g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2217+1896C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786328 | ||||||
| chr4:25786426
|
C | T | 20 | a0001c0001t0002g0126a0001c0001t0002g0139a0001c0001t0002g0302others(17): Show | 20 | HG01192.hp2 HG02145.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.2217+1798G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786426 | ||||||
| chr4:25786564
|
G | A | 2 | a0001c0001t0010g0008a0002c0002t0005g0187 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2217+1660C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786564 | ||||||
| chr4:25786752
|
C | T | 2 | a0005c0019t0002g0010a0016c0020t0002g0011 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2217+1472G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786752 | ||||||
| chr4:25786891
|
G | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0177a0001c0001t0002g0226others(1): Show | 4 | NA18941.hp1 NA19012.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217+1333C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786891 | ||||||
| chr4:25786980
|
T | G | 49 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(46): Show | 49 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.2217+1244A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786980 | ||||||
| chr4:25786985
|
G | C | 2 | a0005c0021t0003g0283a0005c0022t0004g0284 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2217+1239C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786985 | ||||||
| chr4:25787061
|
T | C | 1 | a0001c0001t0002g0177 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2217+1163A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787061 | ||||||
| chr4:25787117
|
T | C | 202 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.2217+1107A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787117 | ||||||
| chr4:25787163
|
C | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0155 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2217+1061G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787163 | ||||||
| chr4:25787169
|
C | A | 2 | a0001c0010t0002g0173a0001c0010t0022g0307 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2217+1055G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787169 | ||||||
| chr4:25787246
|
C | T | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2217+978G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787246 | ||||||
| chr4:25787247
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2217+977C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787247 | ||||||
| chr4:25787383
|
C | T | 26 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0056others(23): Show | 26 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2217+841G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787383 | ||||||
| chr4:25787447
|
G | A | 50 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(47): Show | 50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2217+777C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787447 | ||||||
| chr4:25787691
|
T | C | 50 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(47): Show | 50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2217+533A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787691 | ||||||
| chr4:25787698
|
C | G | 143 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(140): Show | 146 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(143): Show |
intron_variant | MODIFIER | c.2217+526G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787698 | ||||||
| chr4:25787700
|
T | C | 50 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(47): Show | 50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2217+524A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787700 | ||||||
| chr4:25788132
|
A | G | 1 | a0001c0003t0002g0024 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2217+92T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25788132 | ||||||
| chr4:25788154
|
C | T | 1 | a0010c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2217+70G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25788154 | ||||||
| chr4:25788406
|
T | C | 2 | a0001c0001t0003g0216a0001c0001t0003g0265 | 2 | HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2077-42A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788406 | ||||||
| chr4:25788455
|
G | A | 50 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(47): Show | 50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2077-91C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788455 | ||||||
| chr4:25788569
|
C | CGT | 10 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0029others(7): Show | 10 | HG00438.hp2 HG00673.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.2077-207_2077-206d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | ||||||
| chr4:25788569
|
CGT | C | 50 | a0001c0001t0001g0021a0001c0001t0001g0040a0001c0001t0001g0043others(47): Show | 50 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2077-207_2077-206d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | ||||||
| chr4:25788569
|
CGTGT | C | 40 | a0001c0001t0001g0051a0001c0001t0001g0077a0001c0001t0001g0078others(37): Show | 42 | HG01070.hp2 HG01109.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.2077-209_2077-206d others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | ||||||
| chr4:25788569
|
CGTGTGT | C | 120 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(117): Show | 121 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(118): Show |
intron_variant | MODIFIER | c.2077-211_2077-206d others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | ||||||
| chr4:25788569
|
CGTGTGTG others(1): Show |
C | 49 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0047others(46): Show | 49 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.2077-213_2077-206d others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | ||||||
| chr4:25788569
|
CGTGTGTG others(3): Show |
C | 14 | a0001c0001t0002g0099a0001c0001t0002g0126a0001c0001t0002g0128others(11): Show | 14 | HG02145.hp1 HG02630.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.2077-215_2077-206d others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | ||||||
| chr4:25788569
|
CGTGTGTG others(5): Show |
C | 2 | a0001c0010t0002g0173a0001c0010t0022g0307 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2077-217_2077-206d others(14): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | ||||||
| chr4:25788569
|
CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2077-223_2077-206d others(20): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | ||||||
| chr4:25788592
|
G | A | 3 | a0005c0021t0003g0283a0005c0022t0004g0284a0018c0032t0019g0170 | 3 | HG02717.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2077-228C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788592 | ||||||
| chr4:25788594
|
G | A | 11 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0066others(8): Show | 13 | HG02109.hp1 HG02257.hp1 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.2077-230C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788594 | ||||||
| chr4:25788596
|
G | A | 99 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(96): Show | 100 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.2077-232C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788596 | ||||||
| chr4:25788598
|
G | A | 37 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0056others(34): Show | 37 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.2077-234C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788598 | ||||||
| chr4:25788615
|
T | C | 27 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0056others(24): Show | 27 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.2077-251A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788615 | ||||||
| chr4:25788620
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2077-256C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788620 | ||||||
| chr4:25788809
|
G | T | 11 | a0001c0001t0002g0139a0001c0001t0009g0124a0001c0003t0002g0096others(8): Show | 11 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.2077-445C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788809 | ||||||
| chr4:25788898
|
C | G | 1 | a0013c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2077-534G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788898 | ||||||
| chr4:25788899
|
C | G | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2077-535G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788899 | ||||||
| chr4:25788918
|
C | A | 3 | a0001c0001t0008g0114a0001c0001t0008g0290a0011c0029t0005g0135 | 3 | HG01074.hp1 HG01257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2077-554G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788918 | ||||||
| chr4:25788936
|
G | C | 3 | a0001c0001t0002g0128a0001c0001t0002g0134a0001c0001t0002g0151 | 3 | HG03130.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2077-572C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788936 | ||||||
| chr4:25788982
|
T | A | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2077-618A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788982 | ||||||
| chr4:25789021
|
G | T | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2077-657C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789021 | ||||||
| chr4:25789090
|
A | G | 200 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(197): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.2077-726T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789090 | ||||||
| chr4:25789096
|
T | G | 226 | a0001c0001t0001g0012a0001c0001t0001g0030a0001c0001t0001g0035others(223): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2077-732A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789096 | ||||||
| chr4:25789133
|
A | G | 50 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(47): Show | 50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2077-769T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789133 | ||||||
| chr4:25789242
|
G | A | 1 | a0001c0003t0002g0025 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2077-878C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789242 | ||||||
| chr4:25789367
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2077-1003C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789367 | ||||||
| chr4:25789584
|
CA | C | 75 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(72): Show | 75 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.2076+870delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | ||||||
| chr4:25789584
|
CAA | C | 112 | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0036others(109): Show | 115 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.2076+869_2076+870d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | ||||||
| chr4:25789584
|
CAAA | C | 35 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0056others(32): Show | 35 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.2076+868_2076+870d others(5): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | ||||||
| chr4:25789584
|
CAAAA | C | 16 | a0001c0001t0002g0126a0001c0001t0002g0139a0001c0001t0009g0124others(13): Show | 16 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.2076+867_2076+870d others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | ||||||
| chr4:25789584
|
CAAAAA | C | 55 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(52): Show | 55 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.2076+866_2076+870d others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | ||||||
| chr4:25789788
|
C | A | 50 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(47): Show | 50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2076+667G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789788 | ||||||
| chr4:25789791
|
C | A | 2 | a0002c0005t0001g0156a0002c0005t0001g0157 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2076+664G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789791 | ||||||
| chr4:25789807
|
C | A | 1 | a0002c0013t0014g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2076+648G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789807 | ||||||
| chr4:25789812
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2076+643C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789812 | ||||||
| chr4:25789849
|
AG | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0034others(2): Show | 5 | HG01346.hp2 HG01928.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.2076+605delC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789849 | ||||||
| chr4:25789855
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2076+600A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789855 | ||||||
| chr4:25789968
|
T | C | 3 | a0001c0001t0008g0114a0001c0001t0008g0290a0011c0029t0005g0135 | 3 | HG01074.hp1 HG01257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2076+487A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789968 | ||||||
| chr4:25789970
|
T | C | 5 | a0001c0011t0002g0055a0001c0011t0002g0101a0005c0021t0003g0283others(2): Show | 5 | HG02647.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2076+485A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789970 | ||||||
| chr4:25790013
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2076+442A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25790013 | ||||||
| chr4:25790204
|
G | A | 2 | a0001c0011t0002g0055a0001c0011t0002g0101 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2076+251C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25790204 | ||||||
| chr4:25790238
|
C | T | 4 | a0001c0001t0005g0300a0002c0002t0006g0268a0002c0009t0004g0267others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076+217G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25790238 | ||||||
| chr4:25790403
|
C | T | 2 | a0001c0011t0002g0055a0001c0011t0002g0101 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2076+52G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25790403 | ||||||
| chr4:25790610
|
A | AGAAG | 6 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0072others(3): Show | 6 | HG00597.hp2 HG01261.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1957-40_1957-37dup others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | ||||||
| chr4:25790610
|
AGAAG | A | 12 | a0001c0001t0001g0080a0001c0001t0002g0126a0001c0001t0002g0302others(9): Show | 12 | HG01074.hp1 HG01192.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1957-40_1957-37del others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | ||||||
| chr4:25790610
|
AGAAGGAA others(1): Show |
A | 5 | a0001c0001t0002g0139a0002c0009t0003g0278a0004c0007t0001g0165others(2): Show | 5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1957-44_1957-37del others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | ||||||
| chr4:25790610
|
AGAAGGAA others(5): Show |
A | 7 | a0001c0001t0009g0124a0001c0003t0002g0096a0001c0003t0002g0097others(4): Show | 7 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957-48_1957-37del others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | ||||||
| chr4:25790610
|
AGAAGGAA others(13): Show |
A | 2 | a0001c0001t0010g0008a0002c0002t0005g0187 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1957-56_1957-37del others(20): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | ||||||
| chr4:25790610
|
AGAAGGAA others(21): Show |
A | 3 | a0001c0001t0010g0129a0005c0021t0003g0283a0018c0032t0019g0170 | 3 | HG00741.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1957-64_1957-37del others(28): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | ||||||
| chr4:25790610
|
AGAAGGAA others(25): Show |
A | 47 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(44): Show | 47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1957-68_1957-37del others(32): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | ||||||
| chr4:25790621
|
A | G | 1 | a0013c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1957-47T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790621 | ||||||
| chr4:25790626
|
G | A | 1 | a0013c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1957-52C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790626 | ||||||
| chr4:25790632
|
AAGGAAGG others(29): Show |
A | 2 | a0001c0001t0002g0250a0008c0038t0012g0305 | 2 | HG03486.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1957-94_1957-59del others(36): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790632 | ||||||
| chr4:25790632
|
AAGGAAGG others(33): Show |
A | 1 | a0001c0001t0002g0266 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1957-98_1957-59del others(40): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790632 | ||||||
| chr4:25790640
|
AAGGAAGG others(21): Show |
A | 2 | a0001c0011t0002g0055a0001c0011t0002g0101 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1957-94_1957-67del others(28): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790640 | ||||||
| chr4:25790644
|
AAGGAAGG others(17): Show |
A | 7 | a0001c0001t0001g0213a0001c0001t0002g0064a0001c0001t0002g0066others(4): Show | 7 | HG02004.hp1 HG02148.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957-94_1957-71del others(24): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790644 | ||||||
| chr4:25790644
|
AAGGAAGG others(21): Show |
A | 2 | a0001c0001t0001g0204a0001c0001t0018g0233 | 2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1957-98_1957-71del others(28): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790644 | ||||||
| chr4:25790644
|
AAGGAAGG others(25): Show |
A | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1957-102_1957-71de others(33): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790644 | ||||||
| chr4:25790648
|
AAGGAAGG others(13): Show |
A | 3 | a0001c0001t0002g0119a0003c0004t0001g0110a0006c0012t0002g0022 | 3 | HG02735.hp1 NA18968.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1957-94_1957-75del others(20): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790648 | ||||||
| chr4:25790648
|
AAGGAAGG others(17): Show |
A | 57 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(54): Show | 57 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1957-98_1957-75del others(24): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790648 | ||||||
| chr4:25790648
|
AAGGAAGG others(21): Show |
A | 7 | a0001c0001t0001g0235a0001c0001t0001g0256a0001c0001t0002g0069others(4): Show | 7 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.1957-102_1957-75de others(29): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790648 | ||||||
| chr4:25790652
|
AAGGAAGG others(9): Show |
A | 3 | a0001c0010t0024g0309a0001c0014t0001g0159a0001c0027t0001g0197 | 3 | HG00733.hp2 HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1957-94_1957-79del others(16): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790652 | ||||||
| chr4:25790652
|
AAGGAAGG others(13): Show |
A | 20 | a0001c0001t0001g0012a0001c0001t0001g0047a0001c0001t0001g0057others(17): Show | 20 | HG00741.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1957-98_1957-79del others(20): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790652 | ||||||
| chr4:25790652
|
AAGGAAGG others(17): Show |
A | 6 | a0001c0001t0001g0232a0001c0001t0001g0245a0001c0001t0002g0002others(3): Show | 7 | HG00733.hp1 HG01169.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957-102_1957-79de others(25): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790652 | ||||||
| chr4:25790656
|
AAGGAAGG others(5): Show |
A | 2 | a0001c0001t0001g0120a0001c0001t0002g0190 | 2 | HG01069.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1957-94_1957-83del others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790656 | ||||||
| chr4:25790656
|
AAGGAAGG others(9): Show |
A | 9 | a0001c0010t0002g0173a0002c0002t0002g0133a0002c0005t0003g0122others(6): Show | 9 | HG02145.hp2 HG02647.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1957-98_1957-83del others(16): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790656 | ||||||
| chr4:25790656
|
AAGGAAGG others(13): Show |
A | 20 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0041others(17): Show | 20 | HG00609.hp2 HG00738.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1957-102_1957-83de others(21): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790656 | ||||||
| chr4:25790660
|
AAGGAAGG others(1): Show |
A | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0002g0147others(1): Show | 4 | HG00438.hp2 HG00673.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957-94_1957-87del others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790660 | ||||||
| chr4:25790660
|
AAGGAAGG others(5): Show |
A | 3 | a0001c0010t0022g0307a0002c0005t0006g0001a0012c0016t0002g0141 | 5 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1957-98_1957-87del others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790660 | ||||||
| chr4:25790660
|
AAGGAAGG others(9): Show |
A | 4 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0240others(1): Show | 4 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-102_1957-87de others(17): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790660 | ||||||
| chr4:25790664
|
A | G | 8 | a0001c0001t0002g0083a0001c0001t0004g0123a0001c0001t0010g0008others(5): Show | 8 | HG01192.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1957-90T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790664 | ||||||
| chr4:25790664
|
AAGGG | A | 32 | a0001c0001t0001g0040a0001c0001t0001g0051a0001c0001t0001g0081others(29): Show | 32 | HG00558.hp1 HG00558.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.1957-94_1957-91del others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790664 | ||||||
| chr4:25790664
|
AAGGGAGG others(1): Show |
A | 6 | a0001c0001t0001g0075a0001c0001t0002g0046a0001c0001t0003g0086others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957-98_1957-91del others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790664 | ||||||
| chr4:25790664
|
AAGGGAGG others(5): Show |
A | 2 | a0001c0001t0001g0145a0001c0001t0002g0191 | 2 | HG00735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1957-102_1957-91de others(13): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790664 | ||||||
| chr4:25790668
|
G | A | 32 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0072others(29): Show | 32 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1957-94C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790668 | ||||||
| chr4:25790672
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1957-98C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790672 | ||||||
| chr4:25790676
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1957-102C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790676 | ||||||
| chr4:25790705
|
A | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1957-131T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790705 | ||||||
| chr4:25790717
|
A | C | 2 | a0001c0001t0001g0296a0001c0008t0007g0161 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1957-143T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790717 | ||||||
| chr4:25790738
|
A | G | 308 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1957-164T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790738 | ||||||
| chr4:25790742
|
A | G | 308 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1957-168T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790742 | ||||||
| chr4:25790746
|
A | G | 308 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1957-172T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790746 | ||||||
| chr4:25790782
|
G | A | 1 | a0002c0013t0014g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1957-208C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790782 | ||||||
| chr4:25790881
|
T | C | 1 | a0002c0013t0014g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1957-307A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790881 | ||||||
| chr4:25791024
|
G | T | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1957-450C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791024 | ||||||
| chr4:25791094
|
C | T | 50 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(47): Show | 50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1957-520G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791094 | ||||||
| chr4:25791095
|
A | C | 229 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(226): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1957-521T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791095 | ||||||
| chr4:25791273
|
A | G | 2 | a0001c0001t0001g0296a0001c0008t0007g0161 | 2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1957-699T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791273 | ||||||
| chr4:25791436
|
T | C | 146 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(143): Show | 149 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.1957-862A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791436 | ||||||
| chr4:25791459
|
C | T | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1957-885G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791459 | ||||||
| chr4:25791472
|
G | A | 2 | a0001c0011t0002g0055a0001c0011t0002g0101 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1957-898C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791472 | ||||||
| chr4:25791492
|
G | A | 1 | a0001c0001t0002g0272 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1957-918C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791492 | ||||||
| chr4:25791497
|
C | T | 2 | a0001c0001t0002g0152a0002c0002t0008g0301 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1957-923G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791497 | ||||||
| chr4:25791645
|
T | C | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1957-1071A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791645 | ||||||
| chr4:25791772
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1957-1198C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791772 | ||||||
| chr4:25791789
|
G | A | 1 | a0001c0001t0005g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1957-1215C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791789 | ||||||
| chr4:25791861
|
C | G | 3 | a0001c0001t0004g0130a0001c0001t0010g0129a0002c0009t0007g0298 | 3 | HG00741.hp1 HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1957-1287G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791861 | ||||||
| chr4:25791911
|
TA | T | 27 | a0001c0001t0001g0043a0001c0001t0001g0136a0001c0001t0001g0258others(24): Show | 27 | HG01070.hp2 HG01433.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1957-1338delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791911 | ||||||
| chr4:25792053
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1957-1479A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792053 | ||||||
| chr4:25792116
|
C | A | 31 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(28): Show | 31 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1957-1542G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792116 | ||||||
| chr4:25792179
|
G | A | 70 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0136others(67): Show | 72 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1957-1605C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792179 | ||||||
| chr4:25792189
|
G | GT | 4 | a0001c0001t0001g0145a0001c0001t0001g0201a0001c0001t0001g0206others(1): Show | 4 | HG00597.hp2 HG02738.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-1616dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792189 | ||||||
| chr4:25792191
|
A | T | 234 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(231): Show | 237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1957-1617T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792191 | ||||||
| chr4:25792326
|
C | A | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1957-1752G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792326 | ||||||
| chr4:25792372
|
G | A | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1957-1798C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792372 | ||||||
| chr4:25792468
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1957-1894T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792468 | ||||||
| chr4:25792471
|
G | T | 57 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0188others(54): Show | 59 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1957-1897C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792471 | ||||||
| chr4:25792485
|
A | C | 101 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(98): Show | 103 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1957-1911T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792485 | ||||||
| chr4:25792679
|
A | T | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1957-2105T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792679 | ||||||
| chr4:25792823
|
T | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1957-2249A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792823 | ||||||
| chr4:25792954
|
G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1957-2380C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792954 | ||||||
| chr4:25792959
|
T | A | 1 | a0001c0001t0002g0251 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1957-2385A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792959 | ||||||
| chr4:25792961
|
T | A | 4 | a0001c0001t0005g0300a0002c0002t0006g0268a0002c0009t0004g0267others(1): Show | 4 | HG02280.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957-2387A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792961 | ||||||
| chr4:25792973
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1957-2399C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792973 | ||||||
| chr4:25793064
|
C | T | 58 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0188others(55): Show | 60 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1957-2490G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793064 | ||||||
| chr4:25793083
|
G | C | 3 | a0001c0001t0002g0071a0001c0001t0002g0111a0001c0001t0002g0261 | 3 | HG01169.hp2 HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1957-2509C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793083 | ||||||
| chr4:25793159
|
C | T | 32 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(29): Show | 32 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1957-2585G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793159 | ||||||
| chr4:25793220
|
A | G | 33 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(30): Show | 33 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1957-2646T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793220 | ||||||
| chr4:25793247
|
G | A | 96 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(93): Show | 97 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.1957-2673C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793247 | ||||||
| chr4:25793256
|
C | T | 1 | a0001c0006t0004g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1957-2682G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793256 | ||||||
| chr4:25793290
|
T | G | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1957-2716A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793290 | ||||||
| chr4:25793438
|
C | T | 4 | a0001c0001t0010g0008a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02630.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957-2864G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793438 | ||||||
| chr4:25793513
|
T | C | 97 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(94): Show | 98 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.1957-2939A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793513 | ||||||
| chr4:25793558
|
GC | G | 96 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(93): Show | 97 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.1957-2985delG | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793558 | ||||||
| chr4:25793685
|
G | A | 2 | a0002c0005t0001g0156a0002c0005t0001g0157 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1957-3111C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793685 | ||||||
| chr4:25793692
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1957-3118A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793692 | ||||||
| chr4:25793766
|
T | G | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1957-3192A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793766 | ||||||
| chr4:25793770
|
C | T | 1 | a0001c0001t0002g0032 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1957-3196G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793770 | ||||||
| chr4:25793809
|
G | T | 21 | a0001c0001t0001g0188a0001c0001t0001g0287a0001c0001t0001g0288others(18): Show | 23 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1957-3235C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793809 | ||||||
| chr4:25793980
|
A | T | 2 | a0005c0019t0002g0010a0016c0020t0002g0011 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1957-3406T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793980 | ||||||
| chr4:25794013
|
C | T | 54 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0188others(51): Show | 56 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1957-3439G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794013 | ||||||
| chr4:25794028
|
G | A | 2 | a0001c0001t0002g0192a0001c0001t0002g0262 | 2 | HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1957-3454C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794028 | ||||||
| chr4:25794228
|
A | G | 32 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0258others(29): Show | 32 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1957-3654T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794228 | ||||||
| chr4:25794247
|
T | C | 10 | a0001c0001t0001g0136a0001c0001t0002g0148a0001c0001t0002g0152others(7): Show | 10 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1957-3673A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794247 | ||||||
| chr4:25794251
|
A | G | 1 | a0001c0001t0003g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1957-3677T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794251 | ||||||
| chr4:25794271
|
C | A | 2 | a0002c0002t0002g0133a0002c0005t0003g0122 | 2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1957-3697G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794271 | ||||||
| chr4:25794336
|
C | A | 6 | a0001c0001t0004g0123a0001c0001t0010g0008a0002c0002t0008g0301others(3): Show | 6 | HG01192.hp2 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1957-3762G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794336 | ||||||
| chr4:25794540
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1957-3966G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794540 | ||||||
| chr4:25794568
|
A | G | 2 | a0001c0010t0002g0173a0001c0010t0022g0307 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1957-3994T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794568 | ||||||
| chr4:25794574
|
G | A | 22 | a0001c0001t0002g0015a0001c0001t0002g0017a0001c0001t0002g0034others(19): Show | 22 | HG00741.hp1 HG01346.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.1957-4000C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794574 | ||||||
| chr4:25794591
|
T | C | 4 | a0001c0010t0024g0309a0001c0014t0001g0159a0002c0002t0002g0133others(1): Show | 4 | HG01109.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-4017A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794591 | ||||||
| chr4:25794694
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1957-4120G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794694 | ||||||
| chr4:25794697
|
A | C | 1 | a0001c0001t0008g0290 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1957-4123T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794697 | ||||||
| chr4:25794707
|
T | C | 2 | a0001c0001t0002g0196a0001c0034t0002g0137 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1957-4133A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794707 | ||||||
| chr4:25794892
|
C | A | 73 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(70): Show | 75 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1957-4318G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794892 | ||||||
| chr4:25794892
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1957-4318G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794892 | ||||||
| chr4:25794894
|
T | G | 5 | a0001c0001t0002g0302a0002c0002t0002g0277a0002c0002t0002g0281others(2): Show | 5 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1957-4320A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794894 | ||||||
| chr4:25794905
|
G | A | 43 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(40): Show | 43 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1957-4331C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794905 | ||||||
| chr4:25795015
|
T | C | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1957-4441A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795015 | ||||||
| chr4:25795055
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0021others(43): Show | 46 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1957-4481C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795055 | ||||||
| chr4:25795059
|
G | A | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1957-4485C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795059 | ||||||
| chr4:25795060
|
T | TG | 14 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0163others(11): Show | 16 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1957-4487dupC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795060 | ||||||
| chr4:25795154
|
A | C | 7 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0163others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1957-4580T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795154 | ||||||
| chr4:25795155
|
CGT | C | 7 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0163others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1957-4583_1957-458 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795155 | ||||||
| chr4:25795158
|
T | C | 7 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0163others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1957-4584A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795158 | ||||||
| chr4:25795191
|
G | A | 1 | a0002c0005t0006g0001 | 3 | HG02109.hp1 HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1957-4617C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795191 | ||||||
| chr4:25795225
|
A | G | 1 | a0001c0001t0002g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1957-4651T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795225 | ||||||
| chr4:25795322
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG00438.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1957-4748G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795322 | ||||||
| chr4:25795393
|
A | T | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1957-4819T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795393 | ||||||
| chr4:25795463
|
G | C | 74 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(71): Show | 74 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1957-4889C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795463 | ||||||
| chr4:25795595
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1957-5021G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795595 | ||||||
| chr4:25795825
|
C | T | 2 | a0001c0001t0002g0189a0006c0012t0002g0022 | 2 | HG02735.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1957-5251G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795825 | ||||||
| chr4:25795826
|
G | A | 29 | a0001c0001t0001g0104a0001c0001t0001g0117a0001c0001t0001g0188others(26): Show | 30 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1957-5252C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795826 | ||||||
| chr4:25795902
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1957-5328C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795902 | ||||||
| chr4:25795911
|
C | T | 12 | a0001c0001t0001g0296a0001c0001t0002g0302a0001c0008t0007g0161others(9): Show | 12 | HG01884.hp1 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1957-5337G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795911 | ||||||
| chr4:25795924
|
GA | G | 34 | a0001c0001t0001g0012a0001c0001t0001g0100a0001c0001t0001g0287others(31): Show | 36 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1957-5351delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795924 | ||||||
| chr4:25795924
|
GAA | G | 25 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0042others(22): Show | 25 | HG00099.hp2 HG00597.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1957-5352_1957-535 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795924 | ||||||
| chr4:25795946
|
C | T | 1 | a0003c0004t0001g0202 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1957-5372G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795946 | ||||||
| chr4:25795962
|
G | C | 3 | a0002c0002t0008g0301a0002c0009t0007g0298a0010c0037t0003g0304 | 3 | HG02145.hp2 HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1957-5388C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795962 | ||||||
| chr4:25796043
|
A | C | 3 | a0001c0001t0003g0286a0001c0001t0004g0130a0001c0001t0010g0129 | 3 | HG00741.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1957-5469T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796043 | ||||||
| chr4:25796096
|
C | T | 3 | a0001c0001t0008g0114a0001c0001t0008g0290a0011c0029t0005g0135 | 3 | HG01074.hp1 HG01257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1957-5522G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796096 | ||||||
| chr4:25796239
|
C | T | 1 | a0001c0010t0024g0309 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1957-5665G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796239 | ||||||
| chr4:25796253
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1957-5679G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796253 | ||||||
| chr4:25796315
|
T | A | 1 | a0001c0001t0003g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1957-5741A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796315 | ||||||
| chr4:25796321
|
G | A | 3 | a0001c0001t0008g0114a0001c0001t0008g0290a0011c0029t0005g0135 | 3 | HG01074.hp1 HG01257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1957-5747C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796321 | ||||||
| chr4:25796342
|
C | T | 7 | a0001c0001t0002g0196a0001c0001t0009g0285a0001c0014t0001g0159others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1957-5768G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796342 | ||||||
| chr4:25796383
|
C | T | 1 | a0001c0014t0001g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1957-5809G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796383 | ||||||
| chr4:25796449
|
A | ATG | 3 | a0001c0001t0001g0296a0001c0001t0002g0192a0001c0008t0007g0161 | 3 | HG01884.hp1 HG02683.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1956+5832_1956+583 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796449 | ||||||
| chr4:25796697
|
T | C | 158 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(155): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1956+5586A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796697 | ||||||
| chr4:25796713
|
G | A | 1 | a0001c0003t0002g0025 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1956+5570C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796713 | ||||||
| chr4:25796730
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1956+5553C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796730 | ||||||
| chr4:25796864
|
G | C | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1956+5419C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796864 | ||||||
| chr4:25796868
|
GA | G | 86 | a0001c0001t0001g0019a0001c0001t0001g0104a0001c0001t0001g0117others(83): Show | 89 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1956+5414delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796868 | ||||||
| chr4:25796868
|
GAA | G | 7 | a0001c0001t0002g0196a0001c0001t0009g0285a0001c0008t0002g0142others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+5413_1956+541 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796868 | ||||||
| chr4:25796935
|
G | C | 1 | a0001c0010t0002g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1956+5348C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796935 | ||||||
| chr4:25797059
|
G | A | 1 | a0001c0003t0002g0049 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1956+5224C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797059 | ||||||
| chr4:25797153
|
T | C | 132 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(129): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1956+5130A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797153 | ||||||
| chr4:25797193
|
C | CA | 79 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0100others(76): Show | 82 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1956+5089dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797193 | ||||||
| chr4:25797250
|
C | T | 32 | a0001c0001t0002g0126a0001c0001t0002g0302a0002c0002t0001g0279others(29): Show | 34 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1956+5033G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797250 | ||||||
| chr4:25797330
|
T | C | 118 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(115): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1956+4953A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797330 | ||||||
| chr4:25797339
|
C | T | 7 | a0001c0001t0001g0109a0001c0001t0001g0229a0001c0001t0002g0064others(4): Show | 7 | HG01943.hp2 HG02004.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+4944G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797339 | ||||||
| chr4:25797342
|
T | C | 10 | a0001c0001t0002g0302a0002c0002t0002g0277a0002c0002t0002g0281others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1956+4941A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797342 | ||||||
| chr4:25797346
|
A | T | 73 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(70): Show | 74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.1956+4937T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797346 | ||||||
| chr4:25797627
|
A | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0021others(36): Show | 39 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1956+4656T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797627 | ||||||
| chr4:25797715
|
C | A | 2 | a0001c0001t0001g0292a0001c0001t0002g0220 | 2 | HG00738.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1956+4568G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797715 | ||||||
| chr4:25797875
|
A | C | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0296others(5): Show | 8 | HG01074.hp1 HG01884.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1956+4408T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797875 | ||||||
| chr4:25797893
|
G | A | 1 | a0001c0008t0007g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1956+4390C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797893 | ||||||
| chr4:25798092
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0008g0114a0011c0029t0005g0135 | 3 | HG01074.hp1 HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1956+4191C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798092 | ||||||
| chr4:25798130
|
A | C | 157 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.1956+4153T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798130 | ||||||
| chr4:25798133
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1956+4150C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798133 | ||||||
| chr4:25798383
|
T | C | 1 | a0001c0001t0002g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1956+3900A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798383 | ||||||
| chr4:25798442
|
CA | C | 11 | a0002c0002t0002g0133a0002c0002t0002g0138a0002c0002t0008g0301others(8): Show | 13 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1956+3840delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798442 | ||||||
| chr4:25798445
|
A | G | 4 | a0001c0001t0001g0296a0001c0001t0008g0114a0001c0008t0007g0161others(1): Show | 4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+3838T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798445 | ||||||
| chr4:25798476
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1956+3807A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798476 | ||||||
| chr4:25798545
|
C | T | 21 | a0001c0001t0002g0196a0001c0034t0002g0137a0002c0002t0002g0133others(18): Show | 23 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1956+3738G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798545 | ||||||
| chr4:25798657
|
G | A | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1956+3626C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798657 | ||||||
| chr4:25798870
|
G | A | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1956+3413C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798870 | ||||||
| chr4:25798957
|
C | T | 1 | a0001c0001t0003g0276 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1956+3326G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798957 | ||||||
| chr4:25799077
|
TTTG | T | 3 | a0001c0001t0001g0136a0001c0001t0002g0131a0001c0001t0002g0134 | 3 | HG02257.hp2 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1956+3203_1956+320 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799077 | ||||||
| chr4:25799248
|
C | T | 173 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(170): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1956+3035G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799248 | ||||||
| chr4:25799259
|
G | C | 164 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(161): Show | 165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.1956+3024C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799259 | ||||||
| chr4:25799267
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1956+3016C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799267 | ||||||
| chr4:25799519
|
C | T | 2 | a0001c0001t0008g0114a0011c0029t0005g0135 | 2 | HG01074.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1956+2764G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799519 | ||||||
| chr4:25799554
|
G | A | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1956+2729C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799554 | ||||||
| chr4:25799681
|
T | C | 1 | a0007c0031t0020g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1956+2602A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799681 | ||||||
| chr4:25799861
|
T | C | 2 | a0001c0001t0002g0196a0001c0034t0002g0137 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1956+2422A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799861 | ||||||
| chr4:25799906
|
A | G | 2 | a0001c0001t0002g0302a0001c0006t0004g0299 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1956+2377T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799906 | ||||||
| chr4:25799996
|
G | T | 1 | a0001c0008t0007g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1956+2287C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799996 | ||||||
| chr4:25800125
|
G | A | 28 | a0002c0002t0001g0279a0002c0002t0002g0133a0002c0002t0002g0138others(25): Show | 30 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1956+2158C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800125 | ||||||
| chr4:25800255
|
A | C | 1 | a0001c0001t0001g0087 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1956+2028T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800255 | ||||||
| chr4:25800315
|
C | A | 184 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(181): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1956+1968G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800315 | ||||||
| chr4:25800340
|
C | G | 2 | a0001c0001t0002g0295a0001c0008t0001g0162 | 2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1956+1943G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800340 | ||||||
| chr4:25800358
|
A | G | 2 | a0001c0001t0002g0032a0006c0012t0015g0073 | 2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1956+1925T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800358 | ||||||
| chr4:25800616
|
T | C | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1956+1667A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800616 | ||||||
| chr4:25800668
|
T | A | 4 | a0001c0001t0001g0296a0001c0001t0008g0114a0001c0008t0007g0161others(1): Show | 4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+1615A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800668 | ||||||
| chr4:25800669
|
A | T | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1956+1614T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800669 | ||||||
| chr4:25800754
|
G | C | 34 | a0001c0001t0002g0196a0001c0014t0001g0159a0001c0034t0002g0137others(31): Show | 36 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.1956+1529C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800754 | ||||||
| chr4:25800776
|
G | C | 4 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0163others(1): Show | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1956+1507C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800776 | ||||||
| chr4:25800778
|
A | G | 4 | a0001c0001t0001g0296a0001c0001t0008g0114a0001c0008t0007g0161others(1): Show | 4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+1505T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800778 | ||||||
| chr4:25800867
|
A | G | 35 | a0001c0001t0002g0196a0001c0014t0001g0159a0001c0034t0002g0137others(32): Show | 37 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.1956+1416T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800867 | ||||||
| chr4:25800885
|
C | T | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1956+1398G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800885 | ||||||
| chr4:25800930
|
C | G | 6 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0163others(3): Show | 6 | HG02451.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1956+1353G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800930 | ||||||
| chr4:25801030
|
C | T | 1 | a0001c0027t0001g0197 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1956+1253G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801030 | ||||||
| chr4:25801141
|
G | A | 1 | a0001c0014t0001g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1956+1142C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801141 | ||||||
| chr4:25801262
|
G | C | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1956+1021C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801262 | ||||||
| chr4:25801276
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1956+1007C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801276 | ||||||
| chr4:25801311
|
G | A | 46 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(43): Show | 46 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1956+972C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801311 | ||||||
| chr4:25801346
|
T | A | 1 | a0001c0001t0003g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1956+937A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801346 | ||||||
| chr4:25801360
|
G | T | 1 | a0001c0001t0002g0227 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1956+923C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801360 | ||||||
| chr4:25801534
|
C | T | 28 | a0002c0002t0001g0279a0002c0002t0002g0133a0002c0002t0002g0138others(25): Show | 30 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1956+749G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801534 | ||||||
| chr4:25801602
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1956+681A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801602 | ||||||
| chr4:25802115
|
A | C | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+168T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25802115 | ||||||
| chr4:25802208
|
A | G | 203 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(200): Show | 206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.1956+75T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25802208 | ||||||
| chr4:25802486
|
C | T | 28 | a0002c0002t0001g0279a0002c0002t0002g0133a0002c0002t0002g0138others(25): Show | 30 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1777-24G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802486 | ||||||
| chr4:25802621
|
G | A | 28 | a0002c0002t0001g0279a0002c0002t0002g0133a0002c0002t0002g0138others(25): Show | 30 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1777-159C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802621 | ||||||
| chr4:25802726
|
C | T | 1 | a0001c0001t0002g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1777-264G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802726 | ||||||
| chr4:25802943
|
C | T | 1 | a0001c0014t0001g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1777-481G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802943 | ||||||
| chr4:25802959
|
T | C | 1 | a0001c0001t0005g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1777-497A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802959 | ||||||
| chr4:25803229
|
C | T | 10 | a0001c0001t0002g0128a0001c0001t0002g0148a0001c0001t0002g0151others(7): Show | 10 | HG01891.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1777-767G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803229 | ||||||
| chr4:25803296
|
CT | C | 12 | a0001c0001t0001g0038a0001c0001t0001g0077a0001c0001t0001g0084others(9): Show | 12 | HG01358.hp1 HG01943.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1777-835delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803296 | ||||||
| chr4:25803297
|
T | G | 4 | a0001c0001t0001g0296a0001c0001t0008g0114a0001c0008t0007g0161others(1): Show | 4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1777-835A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803297 | ||||||
| chr4:25803306
|
C | A | 1 | a0014c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1777-844G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803306 | ||||||
| chr4:25803327
|
A | G | 159 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(156): Show | 160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1777-865T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803327 | ||||||
| chr4:25803398
|
C | T | 2 | a0001c0001t0003g0149a0001c0001t0006g0150 | 2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1777-936G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803398 | ||||||
| chr4:25803435
|
C | T | 1 | a0014c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1777-973G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803435 | ||||||
| chr4:25803508
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1776+1033C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803508 | ||||||
| chr4:25803569
|
C | T | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1776+972G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803569 | ||||||
| chr4:25803638
|
G | A | 38 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0163others(35): Show | 40 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.1776+903C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803638 | ||||||
| chr4:25803781
|
G | GT | 30 | a0001c0001t0002g0006a0001c0001t0002g0177a0001c0001t0002g0227others(27): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1776+759dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803781 | ||||||
| chr4:25803782
|
T | G | 1 | a0001c0001t0002g0015 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1776+759A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803782 | ||||||
| chr4:25803790
|
T | G | 9 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0020others(6): Show | 9 | HG02451.hp1 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1776+751A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803790 | ||||||
| chr4:25803799
|
G | T | 193 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(190): Show | 196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1776+742C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803799 | ||||||
| chr4:25803805
|
G | T | 1 | a0017c0030t0001g0045 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1776+736C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803805 | ||||||
| chr4:25803928
|
G | A | 1 | a0006c0012t0015g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1776+613C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803928 | ||||||
| chr4:25804306
|
G | A | 1 | a0014c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1776+235C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25804306 | ||||||
| chr4:25804778
|
A | T | 2 | a0001c0001t0001g0080a0001c0001t0002g0094 | 2 | NA18968.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1565-26T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25804778 | ||||||
| chr4:25804803
|
T | C | 1 | a0001c0001t0002g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1565-51A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25804803 | ||||||
| chr4:25805224
|
G | T | 1 | a0001c0001t0002g0226 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1565-472C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805224 | ||||||
| chr4:25805324
|
C | A | 2 | a0001c0001t0001g0274a0001c0001t0002g0178 | 2 | HG00099.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1565-572G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805324 | ||||||
| chr4:25805487
|
C | G | 2 | a0001c0001t0002g0289a0001c0001t0008g0290 | 2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1565-735G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805487 | ||||||
| chr4:25805496
|
C | T | 1 | a0001c0006t0004g0299 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1565-744G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805496 | ||||||
| chr4:25805582
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1565-830T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805582 | ||||||
| chr4:25805592
|
TC | T | 144 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(141): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1565-841delG | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805592 | ||||||
| chr4:25805678
|
TAG | T | 8 | a0001c0001t0002g0139a0001c0001t0004g0123a0001c0001t0009g0124others(5): Show | 8 | HG01192.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1565-928_1565-927d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805678 | ||||||
| chr4:25805698
|
C | G | 1 | a0001c0001t0001g0252 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1565-946G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805698 | ||||||
| chr4:25805708
|
C | T | 1 | a0009c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1565-956G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805708 | ||||||
| chr4:25805897
|
A | G | 1 | a0001c0001t0002g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1565-1145T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805897 | ||||||
| chr4:25806041
|
G | GT | 69 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(66): Show | 69 | HG00140.hp2 HG00558.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.1565-1290dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806041 | ||||||
| chr4:25806041
|
GT | G | 43 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0038others(40): Show | 43 | HG00438.hp2 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1565-1290delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806041 | ||||||
| chr4:25806045
|
T | G | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1565-1293A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806045 | ||||||
| chr4:25806046
|
T | G | 2 | a0001c0001t0003g0149a0001c0001t0006g0150 | 2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1565-1294A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806046 | ||||||
| chr4:25806196
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1565-1444C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806196 | ||||||
| chr4:25806205
|
A | T | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1565-1453T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806205 | ||||||
| chr4:25806251
|
A | G | 1 | a0001c0014t0001g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1565-1499T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806251 | ||||||
| chr4:25806294
|
C | T | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1565-1542G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806294 | ||||||
| chr4:25806478
|
C | G | 2 | a0001c0001t0002g0196a0001c0034t0002g0137 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1565-1726G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806478 | ||||||
| chr4:25806577
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1565-1825C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806577 | ||||||
| chr4:25806856
|
T | TA | 12 | a0001c0001t0001g0296a0001c0001t0002g0174a0001c0001t0002g0196others(9): Show | 12 | HG01074.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1565-2105dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806856 | ||||||
| chr4:25806991
|
C | T | 2 | a0001c0001t0002g0208a0001c0001t0002g0248 | 2 | HG01169.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1565-2239G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806991 | ||||||
| chr4:25807070
|
A | C | 160 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(157): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1565-2318T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807070 | ||||||
| chr4:25807089
|
G | A | 2 | a0001c0008t0007g0161a0012c0016t0002g0141 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1565-2337C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807089 | ||||||
| chr4:25807152
|
C | G | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1565-2400G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807152 | ||||||
| chr4:25807155
|
T | C | 31 | a0001c0001t0002g0302a0001c0001t0005g0300a0001c0006t0004g0299others(28): Show | 33 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1565-2403A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807155 | ||||||
| chr4:25807280
|
G | A | 1 | a0003c0004t0001g0195 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1565-2528C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807280 | ||||||
| chr4:25807448
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1565-2696A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807448 | ||||||
| chr4:25807580
|
A | T | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1565-2828T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807580 | ||||||
| chr4:25807641
|
A | T | 3 | a0001c0001t0002g0264a0001c0001t0003g0216a0001c0001t0003g0265 | 3 | HG00738.hp2 HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1565-2889T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807641 | ||||||
| chr4:25807740
|
C | T | 2 | a0001c0001t0002g0196a0001c0034t0002g0137 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1565-2988G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807740 | ||||||
| chr4:25807783
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1565-3031T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807783 | ||||||
| chr4:25807812
|
A | G | 1 | a0014c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1565-3060T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807812 | ||||||
| chr4:25808202
|
T | C | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1565-3450A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808202 | ||||||
| chr4:25808251
|
A | C | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1565-3499T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808251 | ||||||
| chr4:25808318
|
C | T | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1565-3566G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808318 | ||||||
| chr4:25808360
|
A | G | 4 | a0001c0001t0001g0296a0001c0001t0008g0114a0001c0008t0007g0161others(1): Show | 4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565-3608T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808360 | ||||||
| chr4:25808395
|
T | C | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1565-3643A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808395 | ||||||
| chr4:25808396
|
A | C | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1565-3644T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808396 | ||||||
| chr4:25808474
|
G | A | 67 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0050others(64): Show | 67 | HG00140.hp2 HG00558.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.1565-3722C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808474 | ||||||
| chr4:25808725
|
C | T | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1565-3973G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808725 | ||||||
| chr4:25808739
|
T | C | 2 | a0001c0011t0002g0055a0001c0011t0002g0101 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1565-3987A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808739 | ||||||
| chr4:25808784
|
T | C | 2 | a0001c0003t0002g0096a0001c0003t0002g0097 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1565-4032A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808784 | ||||||
| chr4:25808806
|
A | ACGCCTGT others(129): Show |
3 | a0001c0001t0002g0196a0001c0001t0002g0289a0001c0034t0002g0137 | 3 | HG01433.hp2 HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1565-4055_1565-405 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808806 | ||||||
| chr4:25808815
|
A | ATCCCAGC others(129): Show |
2 | a0001c0001t0001g0201a0001c0001t0001g0218 | 2 | NA18993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1565-4064_1565-406 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808815 | ||||||
| chr4:25808836
|
G | A | 2 | a0001c0003t0002g0096a0001c0003t0002g0097 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1565-4084C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(265): Show |
1 | a0001c0001t0002g0226 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(129): Show |
227 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0030others(224): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1565-4085_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(401): Show |
1 | a0001c0010t0024g0309 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(412): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(265): Show |
1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(265): Show |
9 | a0001c0001t0001g0019a0001c0001t0001g0047a0001c0001t0001g0082others(6): Show | 9 | HG00609.hp1 HG00673.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(265): Show |
28 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0051others(25): Show | 28 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(129): Show |
16 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0084others(13): Show | 16 | HG00609.hp2 HG01074.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.1565-4085_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(265): Show |
1 | a0001c0001t0002g0247 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(129): Show |
1 | a0001c0001t0002g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808836
|
G | GAGGCGGG others(129): Show |
1 | a0001c0001t0001g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | ||||||
| chr4:25808841
|
G | GGGCAGAT others(129): Show |
1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1565-4090_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808841 | ||||||
| chr4:25808870
|
A | C | 14 | a0001c0001t0003g0149a0001c0001t0006g0150a0001c0011t0003g0172others(11): Show | 14 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1565-4118T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808870 | ||||||
| chr4:25808873
|
C | T | 14 | a0001c0001t0003g0149a0001c0001t0006g0150a0001c0011t0003g0172others(11): Show | 14 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1565-4121G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808873 | ||||||
| chr4:25808893
|
C | CCCCCGTC others(128): Show |
1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1565-4142_1565-414 others(139): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808893 | ||||||
| chr4:25808897
|
T | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0075a0001c0001t0001g0193others(3): Show | 6 | HG03579.hp2 NA18747.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1565-4145A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808897 | ||||||
| chr4:25808898
|
A | C | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1565-4146T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808898 | ||||||
| chr4:25808898
|
A | G | 9 | a0001c0001t0001g0040a0001c0001t0001g0075a0001c0001t0001g0193others(6): Show | 9 | HG03098.hp1 HG03579.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565-4146T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808898 | ||||||
| chr4:25808938
|
T | A | 79 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0050others(76): Show | 79 | HG00558.hp1 HG00558.hp2 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.1565-4186A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808938 | ||||||
| chr4:25808943
|
A | G | 1 | a0001c0001t0005g0209 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1565-4191T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808943 | ||||||
| chr4:25808945
|
T | C | 1 | a0001c0001t0005g0209 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1565-4193A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808945 | ||||||
| chr4:25808965
|
T | C | 2 | a0001c0010t0002g0173a0003c0028t0001g0185 | 2 | HG03041.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1565-4213A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808965 | ||||||
| chr4:25808972
|
G | C | 3 | a0001c0010t0002g0173a0002c0002t0002g0138a0003c0028t0001g0185 | 3 | HG03041.hp1 NA18522.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1565-4220C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808972 | ||||||
| chr4:25808990
|
G | A | 2 | a0001c0001t0001g0028a0001c0003t0002g0049 | 2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.1565-4238C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808990 | ||||||
| chr4:25809005
|
A | G | 1 | a0001c0001t0003g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1565-4253T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809005 | ||||||
| chr4:25809012
|
G | T | 1 | a0001c0001t0005g0223 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1565-4260C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809012 | ||||||
| chr4:25809022
|
G | A | 64 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0072others(61): Show | 64 | HG00558.hp1 HG00558.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.1565-4270C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809022 | ||||||
| chr4:25809037
|
C | T | 2 | a0001c0010t0024g0309a0014c0024t0023g0308 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1565-4285G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809037 | ||||||
| chr4:25809051
|
C | T | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0038others(26): Show | 29 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1565-4299G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809051 | ||||||
| chr4:25809072
|
C | CA | 21 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0095others(18): Show | 21 | HG00597.hp1 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1565-4321dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809072 | ||||||
| chr4:25809289
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1565-4537A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809289 | ||||||
| chr4:25809308
|
AT | A | 144 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0050others(141): Show | 146 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.1565-4557delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809308 | ||||||
| chr4:25809436
|
C | T | 2 | a0001c0001t0003g0149a0001c0001t0006g0150 | 2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1565-4684G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809436 | ||||||
| chr4:25809609
|
G | A | 1 | a0009c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1565-4857C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809609 | ||||||
| chr4:25809629
|
C | T | 29 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0051others(26): Show | 29 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1565-4877G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809629 | ||||||
| chr4:25809770
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1565-5018A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809770 | ||||||
| chr4:25809771
|
A | T | 7 | a0001c0010t0002g0173a0002c0002t0002g0138a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1565-5019T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809771 | ||||||
| chr4:25809853
|
T | C | 17 | a0001c0001t0001g0121a0001c0001t0001g0296a0001c0010t0024g0309others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1565-5101A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809853 | ||||||
| chr4:25809920
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1565-5168C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809920 | ||||||
| chr4:25809982
|
C | T | 4 | a0001c0001t0001g0296a0002c0002t0008g0301a0002c0009t0007g0298others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565-5230G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809982 | ||||||
| chr4:25810101
|
T | C | 1 | a0001c0001t0002g0189 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1565-5349A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810101 | ||||||
| chr4:25810267
|
C | A | 27 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0051others(24): Show | 27 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1565-5515G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810267 | ||||||
| chr4:25810270
|
C | T | 10 | a0002c0002t0001g0279a0002c0002t0002g0277a0002c0002t0002g0281others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565-5518G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810270 | ||||||
| chr4:25810402
|
A | C | 110 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036others(107): Show | 112 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(109): Show |
intron_variant | MODIFIER | c.1565-5650T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810402 | ||||||
| chr4:25810473
|
G | A | 10 | a0002c0002t0001g0279a0002c0002t0002g0277a0002c0002t0002g0281others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565-5721C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810473 | ||||||
| chr4:25810721
|
C | G | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1565-5969G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810721 | ||||||
| chr4:25810739
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1565-5987C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810739 | ||||||
| chr4:25810746
|
G | A | 4 | a0001c0001t0001g0296a0002c0002t0008g0301a0002c0009t0007g0298others(1): Show | 4 | HG01884.hp1 HG02258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565-5994C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810746 | ||||||
| chr4:25810765
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0002g0068 | 2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1565-6013C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810765 | ||||||
| chr4:25810831
|
G | A | 1 | a0016c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1565-6079C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810831 | ||||||
| chr4:25810855
|
G | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0051others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1565-6103C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810855 | ||||||
| chr4:25810920
|
C | T | 2 | a0006c0012t0002g0022a0006c0012t0015g0073 | 2 | HG02735.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1565-6168G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810920 | ||||||
| chr4:25810994
|
C | T | 1 | a0001c0010t0024g0309 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1565-6242G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810994 | ||||||
| chr4:25811075
|
A | G | 64 | a0001c0001t0001g0121a0001c0001t0001g0188a0001c0001t0001g0293others(61): Show | 66 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.1565-6323T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811075 | ||||||
| chr4:25811090
|
C | T | 16 | a0001c0001t0002g0128a0001c0001t0002g0134a0001c0001t0002g0139others(13): Show | 16 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1565-6338G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811090 | ||||||
| chr4:25811091
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0003g0194 | 2 | HG02040.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.1565-6339C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811091 | ||||||
| chr4:25811360
|
T | C | 3 | a0001c0001t0001g0121a0001c0010t0024g0309a0014c0024t0023g0308 | 3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1565-6608A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811360 | ||||||
| chr4:25811448
|
G | A | 135 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036others(132): Show | 137 | HG00558.hp1 HG00558.hp2 HG00733.hp2 others(134): Show |
intron_variant | MODIFIER | c.1564+6690C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811448 | ||||||
| chr4:25811461
|
GTCCATAG others(14): Show |
G | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1564+6656_1564+667 others(25): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811461 | ||||||
| chr4:25811465
|
A | G | 1 | a0001c0001t0003g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1564+6673T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811465 | ||||||
| chr4:25811497
|
A | G | 245 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(242): Show | 248 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(245): Show |
intron_variant | MODIFIER | c.1564+6641T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811497 | ||||||
| chr4:25811659
|
C | T | 5 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+6479G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811659 | ||||||
| chr4:25811748
|
G | GT | 20 | a0001c0001t0001g0009a0001c0001t0001g0042a0001c0001t0001g0047others(17): Show | 20 | HG00558.hp2 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1564+6389dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811748 | ||||||
| chr4:25811748
|
GT | G | 24 | a0001c0001t0001g0040a0001c0001t0002g0140a0001c0001t0002g0163others(21): Show | 26 | HG01071.hp2 HG01074.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1564+6389delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811748 | ||||||
| chr4:25811748
|
GTT | G | 16 | a0001c0001t0001g0188a0001c0001t0001g0296a0001c0001t0002g0247others(13): Show | 16 | HG01261.hp1 HG01884.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1564+6388_1564+638 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811748 | ||||||
| chr4:25811761
|
T | G | 1 | a0010c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1564+6377A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811761 | ||||||
| chr4:25811761
|
T | TG | 5 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0004g0130others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564+6376_1564+637 others(5): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811761 | ||||||
| chr4:25811764
|
T | G | 42 | a0001c0001t0001g0038a0001c0001t0001g0041a0001c0001t0001g0107others(39): Show | 42 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1564+6374A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811764 | ||||||
| chr4:25811765
|
TTG | T | 19 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0051others(16): Show | 19 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1564+6371_1564+637 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811765 | ||||||
| chr4:25811766
|
TG | T | 8 | a0001c0001t0001g0198a0001c0001t0001g0234a0001c0001t0001g0271others(5): Show | 8 | HG01891.hp1 HG02027.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564+6371delC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811766 | ||||||
| chr4:25811767
|
G | T | 20 | a0001c0001t0001g0293a0001c0001t0002g0126a0001c0001t0002g0128others(17): Show | 20 | HG00741.hp1 HG01081.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1564+6371C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811767 | ||||||
| chr4:25811770
|
G | T | 2 | a0001c0001t0004g0123a0008c0038t0012g0305 | 2 | HG01192.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1564+6368C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811770 | ||||||
| chr4:25811845
|
A | C | 1 | a0001c0001t0005g0209 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1564+6293T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811845 | ||||||
| chr4:25811923
|
A | G | 17 | a0001c0001t0001g0293a0001c0001t0002g0128a0001c0001t0002g0134others(14): Show | 17 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1564+6215T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811923 | ||||||
| chr4:25811973
|
T | G | 10 | a0002c0002t0001g0279a0002c0002t0002g0277a0002c0002t0002g0281others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564+6165A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811973 | ||||||
| chr4:25812179
|
CG | C | 5 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+5958delC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812179 | ||||||
| chr4:25812264
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1564+5874A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812264 | ||||||
| chr4:25812405
|
T | C | 1 | a0001c0010t0024g0309 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1564+5733A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812405 | ||||||
| chr4:25812714
|
G | GA | 7 | a0001c0001t0001g0048a0001c0001t0001g0232a0001c0001t0002g0126others(4): Show | 7 | HG01109.hp1 HG02056.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1564+5423dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812714 | ||||||
| chr4:25812714
|
GA | G | 24 | a0001c0001t0001g0120a0001c0001t0001g0236a0001c0001t0001g0256others(21): Show | 24 | HG00738.hp2 HG01069.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1564+5423delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812714 | ||||||
| chr4:25812762
|
C | T | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1564+5376G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812762 | ||||||
| chr4:25812815
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1564+5323G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812815 | ||||||
| chr4:25812882
|
G | A | 26 | a0001c0001t0001g0293a0001c0001t0002g0128a0001c0001t0002g0134others(23): Show | 28 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1564+5256C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812882 | ||||||
| chr4:25812936
|
C | T | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0196 | 3 | HG02055.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1564+5202G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812936 | ||||||
| chr4:25813107
|
G | C | 5 | a0001c0003t0002g0024a0001c0003t0002g0025a0001c0003t0002g0103others(2): Show | 5 | HG00558.hp2 HG00733.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564+5031C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813107 | ||||||
| chr4:25813198
|
T | A | 83 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036others(80): Show | 83 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.1564+4940A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813198 | ||||||
| chr4:25813396
|
C | T | 78 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0036others(75): Show | 78 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(75): Show |
intron_variant | MODIFIER | c.1564+4742G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813396 | ||||||
| chr4:25813470
|
T | A | 17 | a0001c0001t0002g0126a0001c0003t0002g0013a0001c0003t0002g0024others(14): Show | 17 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1564+4668A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813470 | ||||||
| chr4:25813541
|
C | T | 2 | a0001c0001t0009g0285a0001c0006t0004g0132 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1564+4597G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813541 | ||||||
| chr4:25813625
|
C | T | 52 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0051others(49): Show | 54 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1564+4513G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813625 | ||||||
| chr4:25813682
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1564+4456C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813682 | ||||||
| chr4:25813705
|
G | A | 5 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+4433C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813705 | ||||||
| chr4:25813803
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1564+4335A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813803 | ||||||
| chr4:25813922
|
C | T | 1 | a0009c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1564+4216G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813922 | ||||||
| chr4:25814032
|
C | T | 11 | a0001c0001t0001g0121a0001c0001t0001g0287a0001c0001t0001g0288others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1564+4106G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814032 | ||||||
| chr4:25814046
|
G | A | 10 | a0002c0002t0001g0279a0002c0002t0002g0277a0002c0002t0002g0281others(7): Show | 10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564+4092C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814046 | ||||||
| chr4:25814182
|
GA | G | 61 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(58): Show | 61 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.1564+3955delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814182 | ||||||
| chr4:25814350
|
G | A | 3 | a0001c0001t0001g0121a0001c0010t0024g0309a0014c0024t0023g0308 | 3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1564+3788C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814350 | ||||||
| chr4:25814426
|
A | G | 113 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(110): Show | 115 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1564+3712T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814426 | ||||||
| chr4:25814449
|
T | A | 43 | a0001c0001t0001g0293a0001c0001t0002g0126a0001c0001t0002g0163others(40): Show | 43 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1564+3689A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814449 | ||||||
| chr4:25814513
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1564+3625A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814513 | ||||||
| chr4:25814662
|
G | GA | 35 | a0001c0001t0002g0126a0001c0001t0002g0163a0001c0001t0002g0259others(32): Show | 35 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1564+3475dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814662 | ||||||
| chr4:25814745
|
C | T | 3 | a0001c0001t0001g0121a0001c0010t0024g0309a0014c0024t0023g0308 | 3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1564+3393G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814745 | ||||||
| chr4:25814765
|
AT | A | 5 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+3372delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814765 | ||||||
| chr4:25814797
|
G | GT | 69 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(66): Show | 71 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1564+3340dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814797 | ||||||
| chr4:25814797
|
G | GTT | 44 | a0001c0001t0001g0293a0001c0001t0002g0126a0001c0001t0002g0163others(41): Show | 44 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1564+3339_1564+334 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814797 | ||||||
| chr4:25814862
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1564+3276C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814862 | ||||||
| chr4:25814970
|
C | A | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1564+3168G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814970 | ||||||
| chr4:25814990
|
G | A | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1564+3148C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814990 | ||||||
| chr4:25814991
|
G | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0060others(1): Show | 4 | NA18955.hp2 NA18973.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1564+3147C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814991 | ||||||
| chr4:25814996
|
G | A | 43 | a0001c0001t0001g0293a0001c0001t0002g0126a0001c0001t0002g0163others(40): Show | 43 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1564+3142C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814996 | ||||||
| chr4:25815013
|
A | G | 176 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(173): Show | 178 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.1564+3125T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815013 | ||||||
| chr4:25815036
|
C | T | 2 | a0001c0003t0002g0024a0001c0003t0002g0025 | 2 | HG01106.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1564+3102G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815036 | ||||||
| chr4:25815069
|
A | G | 1 | a0001c0034t0002g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1564+3069T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815069 | ||||||
| chr4:25815198
|
G | T | 55 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(52): Show | 55 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1564+2940C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815198 | ||||||
| chr4:25815387
|
G | T | 5 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0004g0130others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564+2751C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815387 | ||||||
| chr4:25815443
|
A | G | 8 | a0001c0001t0001g0293a0001c0001t0002g0295a0001c0001t0003g0149others(5): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564+2695T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815443 | ||||||
| chr4:25815526
|
A | G | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1564+2612T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815526 | ||||||
| chr4:25815660
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1564+2478C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815660 | ||||||
| chr4:25815718
|
A | T | 1 | a0001c0001t0001g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1564+2420T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815718 | ||||||
| chr4:25815805
|
C | A | 7 | a0001c0003t0002g0013a0001c0003t0002g0049a0001c0003t0002g0096others(4): Show | 7 | HG00609.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1564+2333G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815805 | ||||||
| chr4:25815867
|
T | TG | 55 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(52): Show | 55 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1564+2270dupC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815867 | ||||||
| chr4:25815871
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1564+2267C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815871 | ||||||
| chr4:25816037
|
A | C | 3 | a0001c0003t0002g0024a0001c0003t0002g0025a0001c0003t0002g0103 | 3 | HG00558.hp2 HG01106.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1564+2101T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816037 | ||||||
| chr4:25816131
|
CATAAT | C | 8 | a0001c0001t0001g0293a0001c0001t0002g0295a0001c0001t0003g0149others(5): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564+2002_1564+200 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816131 | ||||||
| chr4:25816144
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1564+1994T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816144 | ||||||
| chr4:25816239
|
T | A | 1 | a0001c0001t0001g0245 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1564+1899A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816239 | ||||||
| chr4:25816389
|
G | C | 1 | a0007c0031t0020g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1564+1749C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816389 | ||||||
| chr4:25816615
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1564+1523G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816615 | ||||||
| chr4:25816655
|
C | T | 2 | a0001c0001t0003g0149a0001c0001t0006g0150 | 2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1564+1483G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816655 | ||||||
| chr4:25816775
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1564+1363G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816775 | ||||||
| chr4:25816851
|
T | C | 177 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(174): Show | 179 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(176): Show |
intron_variant | MODIFIER | c.1564+1287A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816851 | ||||||
| chr4:25816942
|
C | T | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0196 | 3 | HG02055.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1564+1196G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816942 | ||||||
| chr4:25816955
|
A | G | 55 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(52): Show | 55 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1564+1183T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816955 | ||||||
| chr4:25817045
|
C | G | 1 | a0001c0001t0003g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1564+1093G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817045 | ||||||
| chr4:25817052
|
A | G | 55 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(52): Show | 55 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1564+1086T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817052 | ||||||
| chr4:25817481
|
C | T | 10 | a0001c0001t0001g0293a0001c0001t0002g0163a0001c0001t0002g0295others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564+657G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817481 | ||||||
| chr4:25817486
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1564+652C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817486 | ||||||
| chr4:25817572
|
C | A | 10 | a0001c0001t0001g0293a0001c0001t0002g0163a0001c0001t0002g0295others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564+566G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817572 | ||||||
| chr4:25817596
|
C | T | 5 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+542G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817596 | ||||||
| chr4:25817632
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1564+506A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817632 | ||||||
| chr4:25817678
|
C | G | 171 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(168): Show | 173 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(170): Show |
intron_variant | MODIFIER | c.1564+460G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817678 | ||||||
| chr4:25817706
|
T | C | 3 | a0001c0001t0001g0121a0001c0010t0024g0309a0014c0024t0023g0308 | 3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1564+432A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817706 | ||||||
| chr4:25817812
|
T | A | 66 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(63): Show | 68 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1564+326A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817812 | ||||||
| chr4:25817888
|
G | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0196 | 3 | HG02055.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1564+250C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817888 | ||||||
| chr4:25817901
|
A | G | 1 | a0001c0001t0002g0208 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1564+237T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817901 | ||||||
| chr4:25818369
|
A | AAGAAGAG others(3): Show |
10 | a0001c0001t0001g0293a0001c0001t0002g0163a0001c0001t0002g0295others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1424-92_1424-91ins others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818369 | ||||||
| chr4:25818371
|
G | A | 2 | a0001c0001t0002g0247a0001c0001t0021g0306 | 2 | HG02074.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1424-93C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818371 | ||||||
| chr4:25818491
|
T | C | 2 | a0001c0001t0002g0302a0001c0006t0004g0299 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1424-213A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818491 | ||||||
| chr4:25818535
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0002g0259a0001c0001t0002g0297 | 3 | HG01884.hp1 HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1424-257C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818535 | ||||||
| chr4:25818536
|
G | A | 6 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0004g0130others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1424-258C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818536 | ||||||
| chr4:25818538
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0061 | 3 | NA18955.hp2 NA18973.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1424-260G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818538 | ||||||
| chr4:25818584
|
G | T | 1 | a0001c0001t0005g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1424-306C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818584 | ||||||
| chr4:25818639
|
C | T | 56 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(53): Show | 56 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1424-361G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818639 | ||||||
| chr4:25818694
|
A | G | 56 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(53): Show | 56 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1424-416T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818694 | ||||||
| chr4:25818737
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1424-459G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818737 | ||||||
| chr4:25818973
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1424-695G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818973 | ||||||
| chr4:25818993
|
C | T | 66 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(63): Show | 68 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1424-715G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818993 | ||||||
| chr4:25819180
|
C | T | 56 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(53): Show | 56 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1423+628G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819180 | ||||||
| chr4:25819335
|
AT | A | 56 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(53): Show | 56 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1423+472delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819335 | ||||||
| chr4:25819340
|
A | T | 56 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(53): Show | 56 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.1423+468T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819340 | ||||||
| chr4:25819421
|
C | T | 8 | a0001c0001t0001g0293a0001c0001t0002g0295a0001c0001t0003g0149others(5): Show | 8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1423+387G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819421 | ||||||
| chr4:25819674
|
A | AG | 17 | a0001c0001t0002g0126a0001c0003t0002g0013a0001c0003t0002g0024others(14): Show | 17 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1423+133dupC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819674 | ||||||
| chr4:25820009
|
G | A | 1 | a0005c0021t0003g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1291-69C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820009 | ||||||
| chr4:25820091
|
C | T | 1 | a0001c0001t0008g0290 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1291-151G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820091 | ||||||
| chr4:25820147
|
T | C | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1291-207A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820147 | ||||||
| chr4:25820154
|
G | C | 3 | a0001c0001t0001g0121a0001c0010t0024g0309a0014c0024t0023g0308 | 3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1291-214C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820154 | ||||||
| chr4:25820309
|
AAG | A | 88 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(85): Show | 90 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.1291-371_1291-370d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820309 | ||||||
| chr4:25820413
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1291-473C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820413 | ||||||
| chr4:25820422
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1291-482C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820422 | ||||||
| chr4:25820449
|
T | G | 2 | a0001c0001t0003g0149a0001c0001t0006g0150 | 2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1291-509A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820449 | ||||||
| chr4:25820512
|
G | A | 16 | a0001c0001t0002g0259a0001c0001t0002g0297a0001c0014t0001g0159others(13): Show | 16 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1291-572C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820512 | ||||||
| chr4:25820564
|
C | T | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1291-624G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820564 | ||||||
| chr4:25820579
|
A | G | 10 | a0001c0001t0001g0293a0001c0001t0002g0163a0001c0001t0002g0295others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1291-639T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820579 | ||||||
| chr4:25820659
|
G | A | 116 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(113): Show | 118 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.1291-719C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820659 | ||||||
| chr4:25820721
|
A | ATATATGT others(9): Show |
1 | a0001c0001t0002g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1291-782_1291-781i others(18): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820721 | ||||||
| chr4:25820730
|
T | C | 1 | a0001c0001t0002g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1291-790A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820730 | ||||||
| chr4:25820889
|
C | T | 80 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(77): Show | 82 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1291-949G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820889 | ||||||
| chr4:25820922
|
G | T | 1 | a0001c0001t0002g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1291-982C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820922 | ||||||
| chr4:25820970
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1290+1026G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820970 | ||||||
| chr4:25820992
|
C | T | 1 | a0001c0001t0006g0150 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1290+1004G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820992 | ||||||
| chr4:25820994
|
C | T | 26 | a0001c0001t0002g0126a0001c0003t0002g0013a0001c0003t0002g0024others(23): Show | 26 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1290+1002G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820994 | ||||||
| chr4:25821209
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1290+787T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821209 | ||||||
| chr4:25821251
|
T | C | 10 | a0001c0001t0002g0163a0001c0001t0002g0295a0001c0001t0003g0149others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1290+745A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821251 | ||||||
| chr4:25821270
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1290+726G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821270 | ||||||
| chr4:25821337
|
G | T | 1 | a0001c0001t0006g0150 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1290+659C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821337 | ||||||
| chr4:25821396
|
T | G | 2 | a0001c0017t0002g0144a0007c0033t0007g0171 | 2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1290+600A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821396 | ||||||
| chr4:25821417
|
C | T | 67 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(64): Show | 69 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1290+579G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821417 | ||||||
| chr4:25821453
|
A | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0258a0001c0001t0002g0174others(1): Show | 4 | HG01070.hp2 HG01433.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1290+543T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821453 | ||||||
| chr4:25821462
|
C | T | 2 | a0001c0001t0001g0070a0005c0022t0004g0284 | 2 | HG02717.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1290+534G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821462 | ||||||
| chr4:25821468
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0002g0264 | 2 | HG00738.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1290+528G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821468 | ||||||
| chr4:25821469
|
G | A | 6 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0004g0130others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1290+527C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821469 | ||||||
| chr4:25821692
|
C | T | 66 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(63): Show | 68 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1290+304G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821692 | ||||||
| chr4:25822268
|
G | A | 1 | a0009c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1158-140C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822268 | ||||||
| chr4:25822292
|
G | A | 2 | a0001c0001t0001g0120a0001c0001t0002g0099 | 2 | HG01069.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1158-164C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822292 | ||||||
| chr4:25822395
|
C | G | 85 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(82): Show | 85 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1158-267G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822395 | ||||||
| chr4:25822415
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1158-287G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822415 | ||||||
| chr4:25822487
|
T | C | 7 | a0001c0010t0002g0173a0002c0002t0002g0138a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1158-359A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822487 | ||||||
| chr4:25822574
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1158-446G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822574 | ||||||
| chr4:25822606
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1158-478C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822606 | ||||||
| chr4:25822658
|
G | A | 7 | a0002c0013t0014g0127a0004c0007t0001g0164a0004c0007t0001g0165others(4): Show | 7 | HG02055.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1158-530C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822658 | ||||||
| chr4:25822661
|
G | A | 7 | a0002c0013t0014g0127a0004c0007t0001g0164a0004c0007t0001g0165others(4): Show | 7 | HG02055.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1158-533C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822661 | ||||||
| chr4:25822696
|
C | T | 1 | a0001c0001t0005g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1158-568G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822696 | ||||||
| chr4:25823117
|
G | C | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1158-989C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823117 | ||||||
| chr4:25823386
|
G | A | 68 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(65): Show | 70 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1158-1258C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823386 | ||||||
| chr4:25823463
|
G | A | 6 | a0001c0001t0001g0121a0001c0001t0002g0163a0001c0010t0022g0307others(3): Show | 6 | HG01109.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158-1335C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823463 | ||||||
| chr4:25823478
|
C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1158-1350G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823478 | ||||||
| chr4:25823501
|
C | T | 5 | a0001c0001t0001g0293a0001c0001t0001g0296a0005c0021t0003g0283others(2): Show | 5 | HG01884.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-1373G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823501 | ||||||
| chr4:25823509
|
C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1158-1381G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823509 | ||||||
| chr4:25823510
|
A | G | 18 | a0001c0001t0001g0121a0001c0001t0002g0163a0001c0001t0002g0259others(15): Show | 18 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1158-1382T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823510 | ||||||
| chr4:25823606
|
C | G | 25 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0296others(22): Show | 27 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1158-1478G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823606 | ||||||
| chr4:25823667
|
C | T | 2 | a0001c0001t0002g0259a0001c0001t0002g0297 | 2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1158-1539G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823667 | ||||||
| chr4:25823707
|
A | G | 21 | a0001c0001t0001g0121a0001c0001t0001g0293a0001c0001t0001g0296others(18): Show | 21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1158-1579T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823707 | ||||||
| chr4:25823793
|
A | G | 58 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0107others(55): Show | 58 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1158-1665T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823793 | ||||||
| chr4:25823833
|
G | C | 1 | a0001c0001t0003g0244 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1158-1705C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823833 | ||||||
| chr4:25823874
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1158-1746C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823874 | ||||||
| chr4:25824158
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1158-2030C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824158 | ||||||
| chr4:25824177
|
C | T | 2 | a0009c0036t0002g0303a0010c0037t0003g0304 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1158-2049G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824177 | ||||||
| chr4:25824661
|
G | A | 1 | a0001c0001t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1158-2533C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824661 | ||||||
| chr4:25824695
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1158-2567C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824695 | ||||||
| chr4:25824721
|
A | G | 9 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(6): Show | 9 | HG02258.hp1 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1158-2593T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824721 | ||||||
| chr4:25824772
|
T | A | 1 | a0018c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1158-2644A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824772 | ||||||
| chr4:25824772
|
T | C | 3 | a0005c0021t0003g0283a0005c0022t0004g0284a0016c0020t0002g0011 | 3 | HG02717.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1158-2644A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824772 | ||||||
| chr4:25824808
|
T | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1158-2680A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824808 | ||||||
| chr4:25824865
|
A | G | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1158-2737T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824865 | ||||||
| chr4:25824923
|
T | C | 18 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(15): Show | 18 | HG00741.hp1 HG01074.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1158-2795A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824923 | ||||||
| chr4:25824956
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1158-2828C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824956 | ||||||
| chr4:25824974
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1158-2846C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824974 | ||||||
| chr4:25825022
|
G | T | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1158-2894C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825022 | ||||||
| chr4:25825049
|
T | C | 2 | a0001c0001t0002g0294a0001c0001t0005g0300 | 2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1158-2921A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825049 | ||||||
| chr4:25825057
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1158-2929A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825057 | ||||||
| chr4:25825178
|
C | T | 1 | a0018c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1158-3050G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825178 | ||||||
| chr4:25825282
|
G | A | 3 | a0005c0021t0003g0283a0005c0022t0004g0284a0016c0020t0002g0011 | 3 | HG02717.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1158-3154C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825282 | ||||||
| chr4:25825343
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1158-3215A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825343 | ||||||
| chr4:25825505
|
A | G | 2 | a0001c0001t0010g0008a0001c0034t0002g0137 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1158-3377T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825505 | ||||||
| chr4:25825506
|
T | C | 1 | a0001c0001t0002g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1158-3378A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825506 | ||||||
| chr4:25825665
|
T | C | 4 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0060others(1): Show | 4 | NA18955.hp2 NA18973.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158-3537A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825665 | ||||||
| chr4:25825666
|
A | AT | 128 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0036others(125): Show | 128 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.1158-3539dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | ||||||
| chr4:25825666
|
A | ATT | 20 | a0001c0001t0001g0028a0001c0001t0001g0203a0001c0001t0001g0206others(17): Show | 20 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1158-3540_1158-353 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | ||||||
| chr4:25825666
|
AT | A | 32 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(29): Show | 34 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1158-3539delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | ||||||
| chr4:25825666
|
ATTTT | A | 12 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(9): Show | 12 | HG02055.hp2 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1158-3542_1158-353 others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | ||||||
| chr4:25825666
|
ATTTTT | A | 8 | a0001c0001t0001g0121a0001c0001t0002g0163a0001c0001t0002g0259others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1158-3543_1158-353 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | ||||||
| chr4:25825778
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1158-3650C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825778 | ||||||
| chr4:25825800
|
G | A | 6 | a0002c0002t0002g0138a0002c0005t0001g0156a0002c0005t0001g0157others(3): Show | 8 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1158-3672C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825800 | ||||||
| chr4:25825831
|
C | T | 1 | a0001c0001t0002g0214 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1158-3703G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825831 | ||||||
| chr4:25826229
|
G | A | 9 | a0001c0001t0001g0121a0001c0001t0002g0163a0001c0001t0002g0297others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1157+3869C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826229 | ||||||
| chr4:25826231
|
T | C | 2 | a0001c0001t0010g0008a0001c0034t0002g0137 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1157+3867A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826231 | ||||||
| chr4:25826289
|
C | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1157+3809G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826289 | ||||||
| chr4:25826729
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1157+3369C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826729 | ||||||
| chr4:25826825
|
G | A | 35 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(32): Show | 37 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1157+3273C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826825 | ||||||
| chr4:25826861
|
A | C | 12 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(9): Show | 12 | HG02055.hp1 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1157+3237T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826861 | ||||||
| chr4:25826943
|
C | G | 9 | a0002c0002t0001g0279a0002c0002t0002g0277a0002c0002t0002g0281others(6): Show | 9 | HG02280.hp2 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1157+3155G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826943 | ||||||
| chr4:25827066
|
T | A | 1 | a0003c0004t0001g0212 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1157+3032A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827066 | ||||||
| chr4:25827162
|
T | G | 58 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0001g0175others(55): Show | 58 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1157+2936A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827162 | ||||||
| chr4:25827409
|
C | A | 13 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(10): Show | 13 | HG02145.hp2 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1157+2689G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827409 | ||||||
| chr4:25827426
|
C | T | 1 | a0001c0001t0001g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1157+2672G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827426 | ||||||
| chr4:25827475
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1157+2623G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827475 | ||||||
| chr4:25827478
|
T | C | 14 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(11): Show | 14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1157+2620A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827478 | ||||||
| chr4:25827694
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0002g0088 | 2 | HG02132.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1157+2404G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827694 | ||||||
| chr4:25827756
|
A | G | 2 | a0005c0021t0003g0283a0005c0022t0004g0284 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1157+2342T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827756 | ||||||
| chr4:25827836
|
G | C | 1 | a0016c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1157+2262C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827836 | ||||||
| chr4:25827844
|
A | AGAGGAAG others(149): Show |
1 | a0001c0027t0001g0197 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1157+2253_1157+225 others(160): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827844 | ||||||
| chr4:25828014
|
T | C | 65 | a0001c0001t0001g0009a0001c0001t0001g0121a0001c0001t0001g0136others(62): Show | 67 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.1157+2084A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828014 | ||||||
| chr4:25828125
|
CTA | C | 5 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0004g0130others(2): Show | 5 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1157+1971_1157+197 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828125 | ||||||
| chr4:25828154
|
C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1157+1944G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828154 | ||||||
| chr4:25828156
|
C | A | 3 | a0001c0001t0002g0148a0001c0001t0002g0153a0001c0001t0002g0155 | 3 | HG02559.hp2 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1157+1942G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828156 | ||||||
| chr4:25828294
|
AT | A | 14 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(11): Show | 14 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1157+1803delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828294 | ||||||
| chr4:25828390
|
G | GT | 26 | a0001c0001t0001g0085a0001c0001t0001g0121a0001c0001t0001g0245others(23): Show | 28 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1157+1707dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828390 | ||||||
| chr4:25828393
|
T | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0034t0002g0137 | 3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1157+1705A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828393 | ||||||
| chr4:25828519
|
G | C | 6 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0002g0196others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1157+1579C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828519 | ||||||
| chr4:25828531
|
C | T | 2 | a0005c0019t0002g0010a0016c0020t0002g0011 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1157+1567G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828531 | ||||||
| chr4:25828533
|
C | T | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1157+1565G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828533 | ||||||
| chr4:25828575
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1157+1523C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828575 | ||||||
| chr4:25828616
|
C | G | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1157+1482G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828616 | ||||||
| chr4:25828651
|
C | A | 7 | a0001c0001t0001g0121a0001c0001t0002g0163a0001c0001t0002g0297others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1157+1447G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828651 | ||||||
| chr4:25828663
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1157+1435C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828663 | ||||||
| chr4:25828703
|
A | AT | 5 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0034t0002g0137others(2): Show | 5 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+1394dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828703 | ||||||
| chr4:25829032
|
G | T | 1 | a0001c0001t0003g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1157+1066C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829032 | ||||||
| chr4:25829033
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1157+1065G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829033 | ||||||
| chr4:25829121
|
C | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1157+977G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829121 | ||||||
| chr4:25829237
|
C | T | 5 | a0002c0005t0001g0156a0002c0005t0001g0157a0002c0005t0003g0122others(2): Show | 7 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1157+861G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829237 | ||||||
| chr4:25829252
|
C | A | 13 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(10): Show | 13 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1157+846G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829252 | ||||||
| chr4:25829417
|
G | A | 23 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0002g0126others(20): Show | 23 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1157+681C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829417 | ||||||
| chr4:25829535
|
G | T | 37 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0287others(34): Show | 37 | HG00741.hp1 HG01192.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1157+563C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829535 | ||||||
| chr4:25829542
|
C | T | 8 | a0001c0001t0002g0148a0001c0001t0002g0151a0001c0001t0002g0152others(5): Show | 8 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+556G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829542 | ||||||
| chr4:25829600
|
G | A | 1 | a0002c0009t0007g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1157+498C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829600 | ||||||
| chr4:25829613
|
T | C | 1 | a0014c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1157+485A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829613 | ||||||
| chr4:25829658
|
A | G | 1 | a0003c0004t0001g0210 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1157+440T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829658 | ||||||
| chr4:25829936
|
G | GA | 29 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(26): Show | 29 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1157+161dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829936 | ||||||
| chr4:25830053
|
C | T | 1 | a0001c0003t0002g0013 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1157+45G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25830053 | ||||||
| chr4:25830056
|
G | A | 36 | a0001c0001t0001g0021a0001c0001t0001g0047a0001c0001t0001g0048others(33): Show | 36 | HG00438.hp1 HG00597.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.1157+42C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25830056 | ||||||
| chr4:25830331
|
T | C | 6 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-175A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25830331 | ||||||
| chr4:25830568
|
A | G | 22 | a0001c0001t0001g0009a0001c0001t0001g0287a0001c0001t0001g0288others(19): Show | 22 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1099-412T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25830568 | ||||||
| chr4:25830572
|
T | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0271a0001c0001t0002g0174others(4): Show | 7 | HG00609.hp1 HG02083.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099-416A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25830572 | ||||||
| chr4:25830767
|
C | T | 29 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(26): Show | 29 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1099-611G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25830767 | ||||||
| chr4:25831022
|
T | C | 1 | a0001c0003t0009g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1099-866A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831022 | ||||||
| chr4:25831071
|
T | C | 6 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0003g0286others(3): Show | 6 | HG02451.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-915A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831071 | ||||||
| chr4:25831149
|
C | T | 1 | a0003c0004t0001g0202 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1099-993G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831149 | ||||||
| chr4:25831384
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1099-1228C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831384 | ||||||
| chr4:25831393
|
G | C | 5 | a0002c0005t0001g0156a0002c0005t0001g0157a0002c0005t0003g0122others(2): Show | 7 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099-1237C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831393 | ||||||
| chr4:25831491
|
A | AAAT | 23 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0029others(20): Show | 23 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1099-1338_1099-133 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831491 | ||||||
| chr4:25831491
|
A | AAATAAT | 3 | a0001c0001t0001g0213a0001c0001t0002g0016a0018c0032t0019g0170 | 3 | HG02148.hp1 HG02148.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1099-1341_1099-133 others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831491 | ||||||
| chr4:25831507
|
AATAATT | A | 34 | a0001c0001t0001g0107a0001c0001t0001g0175a0001c0001t0001g0182others(31): Show | 34 | HG00738.hp1 HG00738.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-1357_1099-135 others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831507 | ||||||
| chr4:25831507
|
AATAATTA others(2): Show |
A | 3 | a0001c0001t0002g0294a0001c0001t0004g0130a0001c0001t0005g0300 | 3 | HG02723.hp1 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1099-1360_1099-135 others(13): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831507 | ||||||
| chr4:25831510
|
A | AATT | 6 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0219others(3): Show | 6 | HG02074.hp1 HG02080.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-1357_1099-135 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | ||||||
| chr4:25831510
|
A | T | 5 | a0001c0001t0001g0072a0001c0001t0001g0087a0001c0001t0002g0147others(2): Show | 5 | HG01516.hp1 HG02071.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-1354T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | ||||||
| chr4:25831510
|
AATT | A | 40 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0056others(37): Show | 41 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-1357_1099-135 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | ||||||
| chr4:25831510
|
AATTATT | A | 70 | a0001c0001t0001g0050a0001c0001t0001g0117a0001c0001t0001g0136others(67): Show | 70 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1099-1360_1099-135 others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | ||||||
| chr4:25831510
|
AATTATTA others(2): Show |
A | 21 | a0001c0001t0002g0250a0001c0001t0003g0286a0001c0008t0002g0142others(18): Show | 23 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1099-1363_1099-135 others(13): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | ||||||
| chr4:25831510
|
AATTATTA others(5): Show |
A | 1 | a0001c0001t0002g0111 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1099-1366_1099-135 others(16): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | ||||||
| chr4:25831513
|
T | A | 97 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0028others(94): Show | 97 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1099-1357A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831513 | ||||||
| chr4:25831516
|
T | A | 98 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(95): Show | 99 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1099-1360A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831516 | ||||||
| chr4:25831519
|
T | A | 93 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(90): Show | 94 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1099-1363A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831519 | ||||||
| chr4:25831522
|
T | A | 48 | a0001c0001t0001g0021a0001c0001t0001g0047a0001c0001t0001g0048others(45): Show | 50 | HG00597.hp2 HG01069.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1099-1366A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831522 | ||||||
| chr4:25831525
|
T | A | 13 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0121others(10): Show | 15 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099-1369A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831525 | ||||||
| chr4:25831679
|
C | T | 6 | a0001c0001t0002g0148a0001c0001t0002g0151a0001c0001t0002g0152others(3): Show | 6 | HG02559.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+1316G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831679 | ||||||
| chr4:25831738
|
T | A | 1 | a0018c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1098+1257A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831738 | ||||||
| chr4:25831914
|
C | A | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1098+1081G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831914 | ||||||
| chr4:25831999
|
G | A | 12 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0134others(9): Show | 12 | HG01192.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1098+996C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831999 | ||||||
| chr4:25832184
|
C | T | 19 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0003g0286others(16): Show | 19 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1098+811G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832184 | ||||||
| chr4:25832302
|
A | G | 5 | a0002c0005t0001g0156a0002c0005t0001g0157a0002c0005t0003g0122others(2): Show | 7 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098+693T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832302 | ||||||
| chr4:25832374
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1098+621A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832374 | ||||||
| chr4:25832562
|
A | G | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1098+433T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832562 | ||||||
| chr4:25832632
|
C | G | 257 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(254): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1098+363G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832632 | ||||||
| chr4:25832706
|
A | G | 6 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+289T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832706 | ||||||
| chr4:25832924
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1098+71C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832924 | ||||||
| chr4:25832961
|
C | T | 1 | a0001c0001t0002g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1098+34G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832961 | ||||||
| chr4:25833168
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.983-58C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 4/23 | chr4 | 25833168 | ||||||
| chr4:25833422
|
T | C | 2 | a0001c0001t0001g0009a0001c0011t0003g0172 | 2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.982+26A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 4/23 | chr4 | 25833422 | ||||||
| chr4:25833687
|
C | T | 1 | a0001c0001t0003g0149 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.861-118G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833687 | ||||||
| chr4:25833817
|
A | G | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-248T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833817 | ||||||
| chr4:25833892
|
C | T | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-323G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833892 | ||||||
| chr4:25833900
|
A | T | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.861-331T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833900 | ||||||
| chr4:25833985
|
T | A | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-416A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833985 | ||||||
| chr4:25834008
|
C | T | 2 | a0005c0019t0002g0010a0016c0020t0002g0011 | 2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.861-439G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834008 | ||||||
| chr4:25834022
|
A | G | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-453T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834022 | ||||||
| chr4:25834084
|
G | A | 1 | a0001c0001t0003g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.861-515C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834084 | ||||||
| chr4:25834188
|
C | A | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.861-619G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834188 | ||||||
| chr4:25834622
|
A | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | NA18942.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.860+575T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834622 | ||||||
| chr4:25834847
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.860+350C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834847 | ||||||
| chr4:25834894
|
C | G | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.860+303G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834894 | ||||||
| chr4:25835074
|
C | T | 14 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0003g0286others(11): Show | 14 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.860+123G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25835074 | ||||||
| chr4:25835095
|
CAAG | C | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.860+99_860+101delC others(2): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25835095 | ||||||
| chr4:25835137
|
T | C | 53 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(50): Show | 55 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.860+60A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25835137 | ||||||
| chr4:25835159
|
C | T | 7 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(4): Show | 7 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.860+38G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25835159 | ||||||
| chr4:25835460
|
T | G | 30 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(27): Show | 30 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.734-137A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835460 | ||||||
| chr4:25835595
|
G | A | 2 | a0009c0036t0002g0303a0010c0037t0003g0304 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.734-272C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835595 | ||||||
| chr4:25835602
|
A | G | 4 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0005g0300others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-279T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835602 | ||||||
| chr4:25835688
|
T | C | 140 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(137): Show | 143 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.734-365A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835688 | ||||||
| chr4:25835780
|
A | G | 1 | a0001c0008t0002g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.734-457T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835780 | ||||||
| chr4:25835847
|
G | C | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-524C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835847 | ||||||
| chr4:25835944
|
T | C | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-621A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835944 | ||||||
| chr4:25835950
|
A | T | 30 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(27): Show | 30 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.734-627T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835950 | ||||||
| chr4:25836017
|
C | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0287a0001c0001t0001g0288others(12): Show | 15 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-694G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836017 | ||||||
| chr4:25836096
|
T | A | 1 | a0001c0001t0002g0191 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.734-773A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836096 | ||||||
| chr4:25836506
|
G | A | 3 | a0001c0001t0002g0014a0001c0003t0002g0024a0001c0003t0002g0025 | 3 | HG01106.hp2 HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.734-1183C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836506 | ||||||
| chr4:25836509
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.734-1186C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836509 | ||||||
| chr4:25836533
|
A | T | 216 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.734-1210T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836533 | ||||||
| chr4:25836693
|
G | A | 1 | a0001c0001t0002g0003 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.734-1370C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836693 | ||||||
| chr4:25836792
|
C | T | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1469G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836792 | ||||||
| chr4:25836806
|
G | C | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1483C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836806 | ||||||
| chr4:25836859
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0002g0220 | 2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.734-1536T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836859 | ||||||
| chr4:25836867
|
T | G | 2 | a0001c0001t0002g0002a0001c0001t0002g0023 | 3 | HG00733.hp1 HG01884.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.734-1544A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836867 | ||||||
| chr4:25836904
|
T | C | 95 | a0001c0001t0001g0107a0001c0001t0001g0175a0001c0001t0001g0182others(92): Show | 95 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.734-1581A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836904 | ||||||
| chr4:25837192
|
G | GA | 30 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(27): Show | 30 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.734-1870dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837192 | ||||||
| chr4:25837279
|
G | T | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-1956C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837279 | ||||||
| chr4:25837391
|
A | T | 2 | a0005c0021t0003g0283a0005c0022t0004g0284 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.734-2068T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837391 | ||||||
| chr4:25837537
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.734-2214G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837537 | ||||||
| chr4:25837630
|
G | A | 4 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0005g0300others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-2307C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837630 | ||||||
| chr4:25837784
|
T | C | 2 | a0009c0036t0002g0303a0010c0037t0003g0304 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.734-2461A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837784 | ||||||
| chr4:25837856
|
A | C | 1 | a0003c0004t0001g0212 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.734-2533T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837856 | ||||||
| chr4:25838106
|
G | A | 3 | a0001c0001t0002g0014a0001c0003t0002g0024a0001c0003t0002g0025 | 3 | HG01106.hp2 HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.734-2783C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838106 | ||||||
| chr4:25838186
|
C | T | 1 | a0003c0028t0001g0185 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.734-2863G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838186 | ||||||
| chr4:25838364
|
G | A | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.734-3041C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838364 | ||||||
| chr4:25838369
|
A | T | 2 | a0001c0001t0003g0149a0001c0001t0006g0150 | 2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.734-3046T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838369 | ||||||
| chr4:25838954
|
G | A | 3 | a0001c0001t0001g0074a0001c0001t0002g0190a0001c0001t0002g0191 | 3 | HG00735.hp2 HG02602.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.734-3631C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838954 | ||||||
| chr4:25839167
|
A | G | 75 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(72): Show | 76 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.734-3844T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839167 | ||||||
| chr4:25839413
|
T | C | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-4090A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839413 | ||||||
| chr4:25839426
|
C | A | 7 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(4): Show | 7 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-4103G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839426 | ||||||
| chr4:25839735
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.734-4412G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839735 | ||||||
| chr4:25839821
|
C | CAA | 109 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(106): Show | 109 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.734-4500_734-4499d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839821 | ||||||
| chr4:25839950
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.734-4627C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839950 | ||||||
| chr4:25840377
|
C | T | 14 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0003g0286others(11): Show | 14 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.734-5054G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840377 | ||||||
| chr4:25840485
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.734-5162A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840485 | ||||||
| chr4:25840712
|
T | C | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-5389A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840712 | ||||||
| chr4:25840794
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.734-5471A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840794 | ||||||
| chr4:25840941
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.734-5618T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840941 | ||||||
| chr4:25841090
|
TGG | T | 6 | a0001c0014t0001g0159a0002c0005t0001g0156a0002c0005t0001g0157others(3): Show | 8 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-5769_734-5768d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841090 | ||||||
| chr4:25841132
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.734-5809T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841132 | ||||||
| chr4:25841218
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.734-5895C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841218 | ||||||
| chr4:25841281
|
G | A | 1 | a0018c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.734-5958C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841281 | ||||||
| chr4:25841388
|
T | C | 1 | a0005c0022t0004g0284 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.733+5906A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841388 | ||||||
| chr4:25841445
|
T | A | 3 | a0001c0008t0002g0142a0001c0008t0012g0143a0012c0016t0002g0141 | 3 | HG02258.hp2 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.733+5849A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841445 | ||||||
| chr4:25841694
|
C | T | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.733+5600G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841694 | ||||||
| chr4:25842117
|
T | C | 3 | a0001c0001t0002g0272a0001c0003t0002g0096a0001c0003t0002g0097 | 3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.733+5177A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842117 | ||||||
| chr4:25842171
|
C | T | 1 | a0001c0027t0001g0197 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.733+5123G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842171 | ||||||
| chr4:25842245
|
T | TA | 15 | a0001c0001t0001g0098a0001c0001t0001g0182a0001c0001t0001g0252others(12): Show | 17 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.733+5048dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842245 | ||||||
| chr4:25842246
|
A | T | 2 | a0009c0036t0002g0303a0010c0037t0003g0304 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.733+5048T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842246 | ||||||
| chr4:25842308
|
A | C | 10 | a0001c0014t0001g0159a0002c0005t0001g0156a0002c0005t0001g0157others(7): Show | 12 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.733+4986T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842308 | ||||||
| chr4:25842398
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.733+4896C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842398 | ||||||
| chr4:25842399
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0002g0083a0001c0001t0002g0105 | 3 | HG00673.hp2 NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.733+4895G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842399 | ||||||
| chr4:25842437
|
G | A | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+4857C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842437 | ||||||
| chr4:25842535
|
G | T | 4 | a0005c0019t0002g0010a0005c0021t0003g0283a0005c0022t0004g0284others(1): Show | 4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+4759C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842535 | ||||||
| chr4:25842550
|
G | A | 11 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(8): Show | 13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4744C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842550 | ||||||
| chr4:25842732
|
G | A | 11 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(8): Show | 13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4562C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842732 | ||||||
| chr4:25842757
|
A | G | 11 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(8): Show | 13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4537T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842757 | ||||||
| chr4:25842774
|
G | A | 4 | a0001c0001t0002g0294a0001c0001t0002g0302a0001c0001t0005g0300others(1): Show | 4 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+4520C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842774 | ||||||
| chr4:25842783
|
T | TC | 11 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(8): Show | 13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4510dupG | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842783 | ||||||
| chr4:25842827
|
T | C | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733+4467A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842827 | ||||||
| chr4:25842918
|
C | T | 11 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(8): Show | 13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4376G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842918 | ||||||
| chr4:25842953
|
T | A | 10 | a0001c0001t0002g0128a0001c0001t0002g0134a0001c0001t0002g0139others(7): Show | 10 | HG01192.hp2 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.733+4341A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842953 | ||||||
| chr4:25842963
|
G | A | 6 | a0001c0014t0001g0159a0002c0005t0001g0156a0002c0005t0001g0157others(3): Show | 8 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.733+4331C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842963 | ||||||
| chr4:25842990
|
G | A | 1 | a0001c0001t0002g0177 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.733+4304C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842990 | ||||||
| chr4:25843014
|
A | T | 10 | a0001c0014t0001g0159a0002c0005t0001g0156a0002c0005t0001g0157others(7): Show | 12 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.733+4280T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843014 | ||||||
| chr4:25843068
|
T | C | 11 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(8): Show | 13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4226A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843068 | ||||||
| chr4:25843129
|
G | A | 11 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(8): Show | 13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4165C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843129 | ||||||
| chr4:25843174
|
G | C | 3 | a0001c0001t0001g0100a0001c0001t0002g0054a0001c0001t0002g0099 | 3 | HG02683.hp2 HG02698.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.733+4120C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843174 | ||||||
| chr4:25843187
|
G | A | 7 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+4107C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843187 | ||||||
| chr4:25843294
|
C | T | 1 | a0001c0001t0011g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.733+4000G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843294 | ||||||
| chr4:25843354
|
C | T | 1 | a0007c0033t0007g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.733+3940G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843354 | ||||||
| chr4:25843428
|
C | T | 6 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+3866G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843428 | ||||||
| chr4:25843436
|
G | A | 1 | a0001c0001t0003g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.733+3858C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843436 | ||||||
| chr4:25843648
|
G | T | 7 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+3646C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843648 | ||||||
| chr4:25843751
|
A | T | 1 | a0001c0001t0010g0129 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.733+3543T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843751 | ||||||
| chr4:25843796
|
G | A | 7 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+3498C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843796 | ||||||
| chr4:25843829
|
G | A | 2 | a0001c0011t0002g0055a0001c0011t0002g0101 | 2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.733+3465C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843829 | ||||||
| chr4:25843895
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.733+3399C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843895 | ||||||
| chr4:25844125
|
C | T | 1 | a0013c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.733+3169G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844125 | ||||||
| chr4:25844290
|
C | G | 7 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+3004G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844290 | ||||||
| chr4:25844327
|
T | C | 7 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+2967A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844327 | ||||||
| chr4:25844339
|
G | A | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.733+2955C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844339 | ||||||
| chr4:25844373
|
T | C | 8 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.733+2921A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844373 | ||||||
| chr4:25844484
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.733+2810C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844484 | ||||||
| chr4:25844609
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.733+2685C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844609 | ||||||
| chr4:25844751
|
C | T | 246 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(243): Show | 249 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.733+2543G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844751 | ||||||
| chr4:25844755
|
A | C | 95 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 98 | HG00597.hp2 HG00733.hp1 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.733+2539T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844755 | ||||||
| chr4:25845125
|
C | T | 5 | a0001c0001t0002g0163a0001c0010t0022g0307a0001c0010t0024g0309others(2): Show | 5 | HG01109.hp1 HG02615.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+2169G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845125 | ||||||
| chr4:25845166
|
G | A | 1 | a0018c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.733+2128C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845166 | ||||||
| chr4:25845372
|
C | T | 7 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+1922G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845372 | ||||||
| chr4:25845412
|
T | C | 7 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+1882A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845412 | ||||||
| chr4:25845426
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.733+1868C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845426 | ||||||
| chr4:25845636
|
G | A | 7 | a0001c0001t0010g0008a0001c0014t0001g0159a0002c0005t0001g0156others(4): Show | 9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+1658C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845636 | ||||||
| chr4:25845693
|
C | CAAGAAAT others(311): Show |
1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+1600_733+1601i others(320): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845693 | ||||||
| chr4:25845929
|
T | C | 134 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(131): Show | 137 | HG00597.hp2 HG00733.hp1 HG00741.hp1 others(134): Show |
intron_variant | MODIFIER | c.733+1365A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845929 | ||||||
| chr4:25845983
|
G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+1311C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845983 | ||||||
| chr4:25845999
|
T | C | 1 | a0001c0001t0002g0200 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.733+1295A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845999 | ||||||
| chr4:25846101
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+1193A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846101 | ||||||
| chr4:25846240
|
C | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+1054G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846240 | ||||||
| chr4:25846269
|
G | A | 10 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0040others(7): Show | 10 | HG00438.hp2 HG00673.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.733+1025C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846269 | ||||||
| chr4:25846434
|
G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+860C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846434 | ||||||
| chr4:25846603
|
A | G | 2 | a0001c0001t0002g0297a0002c0009t0007g0298 | 2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.733+691T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846603 | ||||||
| chr4:25846649
|
C | T | 1 | a0012c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.733+645G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846649 | ||||||
| chr4:25846675
|
A | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+619T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846675 | ||||||
| chr4:25846746
|
T | C | 56 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(53): Show | 57 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.733+548A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846746 | ||||||
| chr4:25846912
|
C | CA | 201 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(198): Show | 204 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(201): Show |
intron_variant | MODIFIER | c.733+381dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846912 | ||||||
| chr4:25846912
|
C | CAA | 26 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0296others(23): Show | 26 | HG01884.hp1 HG02132.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.733+380_733+381dup others(2): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846912 | ||||||
| chr4:25846990
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.733+304C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846990 | ||||||
| chr4:25847015
|
C | A | 1 | a0001c0001t0002g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.733+279G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25847015 | ||||||
| chr4:25847922
|
C | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-58G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25847922 | ||||||
| chr4:25848042
|
C | G | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0003c0004t0001g0146 | 3 | NA18942.hp1 NA18968.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.163-178G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848042 | ||||||
| chr4:25848402
|
G | A | 6 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-538C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848402 | ||||||
| chr4:25848456
|
T | C | 6 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-592A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848456 | ||||||
| chr4:25848487
|
A | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-623T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848487 | ||||||
| chr4:25848497
|
A | G | 1 | a0001c0001t0003g0273 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.163-633T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848497 | ||||||
| chr4:25848533
|
T | G | 6 | a0001c0001t0002g0294a0001c0001t0002g0297a0001c0001t0002g0302others(3): Show | 6 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-669A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848533 | ||||||
| chr4:25848580
|
G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-716C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848580 | ||||||
| chr4:25848651
|
T | C | 2 | a0005c0021t0003g0283a0005c0022t0004g0284 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.163-787A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848651 | ||||||
| chr4:25848702
|
C | T | 40 | a0001c0001t0001g0136a0001c0001t0001g0287a0001c0001t0001g0288others(37): Show | 42 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.163-838G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848702 | ||||||
| chr4:25848757
|
C | G | 56 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(53): Show | 57 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.163-893G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848757 | ||||||
| chr4:25848787
|
G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-923C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848787 | ||||||
| chr4:25848802
|
G | A | 13 | a0001c0001t0001g0009a0001c0001t0001g0293a0001c0001t0001g0296others(10): Show | 13 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-938C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848802 | ||||||
| chr4:25848855
|
C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-991G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848855 | ||||||
| chr4:25848902
|
G | A | 1 | a0016c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.163-1038C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848902 | ||||||
| chr4:25848905
|
C | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1041G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848905 | ||||||
| chr4:25849001
|
A | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1137T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849001 | ||||||
| chr4:25849043
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-1179C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849043 | ||||||
| chr4:25849288
|
C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1424G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849288 | ||||||
| chr4:25849290
|
A | G | 42 | a0001c0001t0001g0136a0001c0001t0001g0287a0001c0001t0001g0288others(39): Show | 44 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.163-1426T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849290 | ||||||
| chr4:25849294
|
A | T | 1 | a0001c0001t0001g0079 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.163-1430T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849294 | ||||||
| chr4:25849454
|
G | A | 1 | a0002c0002t0002g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-1590C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849454 | ||||||
| chr4:25849534
|
G | A | 1 | a0002c0002t0002g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-1670C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849534 | ||||||
| chr4:25849540
|
A | G | 77 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(74): Show | 78 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.163-1676T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849540 | ||||||
| chr4:25849641
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(90): Show | 94 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.163-1777G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849641 | ||||||
| chr4:25849738
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1874A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849738 | ||||||
| chr4:25849826
|
A | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1962T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849826 | ||||||
| chr4:25849993
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.163-2129G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849993 | ||||||
| chr4:25849994
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-2130C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849994 | ||||||
| chr4:25850014
|
G | C | 1 | a0001c0001t0002g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.163-2150C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850014 | ||||||
| chr4:25850084
|
T | G | 41 | a0001c0001t0001g0136a0001c0001t0001g0287a0001c0001t0001g0288others(38): Show | 43 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.163-2220A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850084 | ||||||
| chr4:25850097
|
T | C | 41 | a0001c0001t0001g0136a0001c0001t0001g0287a0001c0001t0001g0288others(38): Show | 43 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.163-2233A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850097 | ||||||
| chr4:25850133
|
A | G | 41 | a0001c0001t0001g0136a0001c0001t0001g0287a0001c0001t0001g0288others(38): Show | 43 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.163-2269T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850133 | ||||||
| chr4:25850144
|
T | C | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-2280A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850144 | ||||||
| chr4:25850166
|
T | C | 15 | a0001c0001t0003g0286a0001c0001t0009g0285a0002c0002t0001g0279others(12): Show | 15 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.163-2302A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850166 | ||||||
| chr4:25850240
|
G | C | 1 | a0001c0001t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.163-2376C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850240 | ||||||
| chr4:25850402
|
C | A | 4 | a0001c0010t0022g0307a0001c0010t0024g0309a0008c0038t0012g0305others(1): Show | 4 | HG01109.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2538G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850402 | ||||||
| chr4:25850503
|
A | C | 1 | a0001c0010t0022g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163-2639T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850503 | ||||||
| chr4:25850721
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0002g0207 | 2 | NA19000.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.163-2857G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850721 | ||||||
| chr4:25850806
|
G | T | 1 | a0001c0001t0002g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.163-2942C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850806 | ||||||
| chr4:25850829
|
T | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-2965A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850829 | ||||||
| chr4:25850857
|
G | GT | 8 | a0001c0001t0001g0043a0001c0001t0001g0056a0001c0001t0001g0057others(5): Show | 8 | HG00597.hp2 HG01074.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2994dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850857 | ||||||
| chr4:25850872
|
T | A | 246 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(243): Show | 249 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(246): Show |
intron_variant | MODIFIER | c.163-3008A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850872 | ||||||
| chr4:25851012
|
G | A | 6 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-3148C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851012 | ||||||
| chr4:25851149
|
C | T | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.163-3285G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851149 | ||||||
| chr4:25851210
|
A | G | 24 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(21): Show | 25 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-3346T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851210 | ||||||
| chr4:25851430
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0078 | 2 | NA18955.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.163-3566C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851430 | ||||||
| chr4:25851692
|
C | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(21): Show | 25 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-3828G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851692 | ||||||
| chr4:25851714
|
C | T | 1 | a0009c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.163-3850G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851714 | ||||||
| chr4:25851717
|
C | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(21): Show | 25 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-3853G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851717 | ||||||
| chr4:25851746
|
G | A | 59 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0287others(56): Show | 61 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.163-3882C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851746 | ||||||
| chr4:25851772
|
C | T | 6 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-3908G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851772 | ||||||
| chr4:25851814
|
G | A | 3 | a0001c0008t0002g0142a0001c0008t0012g0143a0012c0016t0002g0141 | 3 | HG02258.hp2 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.163-3950C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851814 | ||||||
| chr4:25851846
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-3982C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851846 | ||||||
| chr4:25851887
|
C | CA | 72 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0118others(69): Show | 75 | HG00597.hp2 HG00733.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.163-4024dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851887 | ||||||
| chr4:25851887
|
C | CAA | 7 | a0001c0001t0001g0012a0001c0001t0001g0287a0001c0001t0001g0288others(4): Show | 7 | HG01358.hp2 HG01928.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-4025_163-4024d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851887 | ||||||
| chr4:25851908
|
G | A | 59 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0287others(56): Show | 61 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.163-4044C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851908 | ||||||
| chr4:25852081
|
G | A | 9 | a0002c0002t0001g0279a0002c0002t0002g0277a0002c0002t0002g0281others(6): Show | 9 | HG02280.hp2 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-4217C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852081 | ||||||
| chr4:25852152
|
C | G | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.163-4288G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852152 | ||||||
| chr4:25852414
|
T | C | 60 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0287others(57): Show | 62 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-4550A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852414 | ||||||
| chr4:25852840
|
A | G | 97 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(94): Show | 100 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(97): Show |
intron_variant | MODIFIER | c.163-4976T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852840 | ||||||
| chr4:25852844
|
G | A | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163-4980C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852844 | ||||||
| chr4:25852916
|
C | T | 60 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0287others(57): Show | 62 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-5052G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852916 | ||||||
| chr4:25853173
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.163-5309G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853173 | ||||||
| chr4:25853417
|
G | A | 16 | a0001c0001t0001g0009a0001c0001t0003g0286a0001c0001t0009g0285others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-5553C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853417 | ||||||
| chr4:25853488
|
T | C | 60 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0287others(57): Show | 62 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-5624A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853488 | ||||||
| chr4:25853557
|
A | G | 23 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(20): Show | 24 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-5693T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853557 | ||||||
| chr4:25853632
|
A | G | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163-5768T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853632 | ||||||
| chr4:25853633
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163-5769G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853633 | ||||||
| chr4:25853664
|
C | CT | 15 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0175others(12): Show | 15 | HG00609.hp1 HG00741.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.163-5801dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853664 | ||||||
| chr4:25853664
|
CT | C | 130 | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0036others(127): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.163-5801delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853664 | ||||||
| chr4:25853664
|
CTT | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(28): Show | 32 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.163-5802_163-5801d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853664 | ||||||
| chr4:25853967
|
C | T | 1 | a0001c0001t0001g0012 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.163-6103G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853967 | ||||||
| chr4:25854023
|
G | A | 43 | a0001c0001t0001g0136a0001c0001t0001g0287a0001c0001t0001g0288others(40): Show | 45 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.163-6159C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854023 | ||||||
| chr4:25854104
|
G | A | 96 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(93): Show | 99 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.163-6240C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854104 | ||||||
| chr4:25854118
|
T | C | 6 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-6254A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854118 | ||||||
| chr4:25854262
|
G | A | 10 | a0001c0001t0001g0293a0001c0001t0001g0296a0001c0001t0002g0294others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-6398C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854262 | ||||||
| chr4:25854317
|
G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-6453C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854317 | ||||||
| chr4:25854410
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-6546A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854410 | ||||||
| chr4:25854553
|
C | T | 5 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0001t0004g0123others(2): Show | 5 | HG01192.hp2 HG02145.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-6689G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854553 | ||||||
| chr4:25854659
|
G | A | 60 | a0001c0001t0001g0009a0001c0001t0001g0136a0001c0001t0001g0287others(57): Show | 62 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-6795C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854659 | ||||||
| chr4:25854667
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.163-6803C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854667 | ||||||
| chr4:25854675
|
T | A | 1 | a0003c0004t0001g0110 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.163-6811A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854675 | ||||||
| chr4:25855522
|
G | A | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162+7153C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855522 | ||||||
| chr4:25855590
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+7085A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855590 | ||||||
| chr4:25855636
|
C | A | 1 | a0004c0007t0002g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.162+7039G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855636 | ||||||
| chr4:25855693
|
G | A | 2 | a0001c0001t0002g0139a0001c0001t0002g0140 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.162+6982C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855693 | ||||||
| chr4:25855704
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+6971A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855704 | ||||||
| chr4:25855779
|
T | C | 22 | a0001c0001t0001g0009a0001c0001t0003g0286a0001c0001t0009g0285others(19): Show | 22 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.162+6896A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855779 | ||||||
| chr4:25855950
|
C | T | 43 | a0001c0001t0001g0136a0001c0001t0001g0287a0001c0001t0001g0288others(40): Show | 45 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.162+6725G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855950 | ||||||
| chr4:25856018
|
G | A | 83 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0198others(80): Show | 83 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+6657C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856018 | ||||||
| chr4:25856143
|
C | A | 16 | a0001c0001t0001g0009a0001c0001t0003g0286a0001c0001t0009g0285others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.162+6532G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856143 | ||||||
| chr4:25856230
|
T | C | 16 | a0001c0001t0001g0009a0001c0001t0003g0286a0001c0001t0009g0285others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.162+6445A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856230 | ||||||
| chr4:25856368
|
G | A | 7 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(4): Show | 7 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+6307C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856368 | ||||||
| chr4:25856399
|
A | G | 1 | a0007c0033t0007g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162+6276T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856399 | ||||||
| chr4:25856483
|
A | G | 12 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+6192T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856483 | ||||||
| chr4:25856593
|
T | TA | 31 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0118others(28): Show | 32 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.162+6081dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856593 | ||||||
| chr4:25856593
|
TA | T | 36 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0044others(33): Show | 38 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+6081delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856593 | ||||||
| chr4:25856593
|
TAAA | T | 11 | a0001c0001t0003g0286a0001c0001t0010g0008a0002c0002t0001g0279others(8): Show | 11 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+6079_162+6081d others(5): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856593 | ||||||
| chr4:25856604
|
A | C | 12 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+6071T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856604 | ||||||
| chr4:25856608
|
A | C | 40 | a0001c0001t0001g0136a0001c0001t0002g0126a0001c0001t0002g0128others(37): Show | 42 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.162+6067T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856608 | ||||||
| chr4:25856609
|
A | C | 6 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(3): Show | 6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+6066T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856609 | ||||||
| chr4:25856610
|
A | C | 1 | a0001c0001t0002g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.162+6065T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856610 | ||||||
| chr4:25856611
|
A | C | 2 | a0005c0021t0003g0283a0005c0022t0004g0284 | 2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.162+6064T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856611 | ||||||
| chr4:25856801
|
A | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+5874T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856801 | ||||||
| chr4:25857192
|
A | G | 1 | a0001c0001t0002g0177 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.162+5483T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25857192 | ||||||
| chr4:25857214
|
A | T | 23 | a0001c0001t0001g0012a0001c0001t0001g0019a0001c0001t0001g0021others(20): Show | 24 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+5461T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25857214 | ||||||
| chr4:25857517
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+5158A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25857517 | ||||||
| chr4:25857527
|
T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+5148A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25857527 | ||||||
| chr4:25858027
|
G | A | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.162+4648C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858027 | ||||||
| chr4:25858345
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG00438.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.162+4330G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858345 | ||||||
| chr4:25858397
|
T | C | 1 | a0001c0001t0002g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.162+4278A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858397 | ||||||
| chr4:25858484
|
A | C | 6 | a0002c0002t0001g0279a0002c0002t0002g0277a0002c0002t0002g0281others(3): Show | 6 | HG02572.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+4191T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858484 | ||||||
| chr4:25858515
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.162+4160A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858515 | ||||||
| chr4:25858539
|
T | G | 1 | a0001c0001t0001g0040 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.162+4136A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858539 | ||||||
| chr4:25858822
|
G | C | 2 | a0001c0011t0003g0172a0018c0032t0019g0170 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+3853C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858822 | ||||||
| chr4:25859132
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.162+3543T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859132 | ||||||
| chr4:25859175
|
G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+3500C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859175 | ||||||
| chr4:25859328
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0003g0286a0001c0001t0009g0285others(13): Show | 16 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.162+3347G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859328 | ||||||
| chr4:25859737
|
T | C | 103 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(100): Show | 106 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(103): Show |
intron_variant | MODIFIER | c.162+2938A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859737 | ||||||
| chr4:25859790
|
C | A | 12 | a0001c0008t0001g0162a0001c0008t0002g0142a0001c0008t0007g0161others(9): Show | 14 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.162+2885G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859790 | ||||||
| chr4:25859951
|
A | C | 7 | a0004c0007t0001g0164a0004c0007t0001g0165a0004c0007t0001g0166others(4): Show | 7 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+2724T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859951 | ||||||
| chr4:25859965
|
G | A | 1 | a0001c0001t0002g0007 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.162+2710C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859965 | ||||||
| chr4:25860022
|
G | A | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162+2653C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860022 | ||||||
| chr4:25860216
|
T | C | 4 | a0001c0001t0001g0263a0001c0001t0002g0264a0001c0001t0002g0266others(1): Show | 4 | HG00738.hp2 HG00741.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+2459A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860216 | ||||||
| chr4:25860567
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.162+2108G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860567 | ||||||
| chr4:25860586
|
AAATGTGG others(12): Show |
A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+2070_162+2088d others(21): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860586 | ||||||
| chr4:25860844
|
C | G | 1 | a0018c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162+1831G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860844 | ||||||
| chr4:25860904
|
T | A | 1 | a0001c0001t0002g0302 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+1771A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860904 | ||||||
| chr4:25860974
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.162+1701T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860974 | ||||||
| chr4:25861086
|
G | C | 52 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(49): Show | 53 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.162+1589C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861086 | ||||||
| chr4:25861163
|
G | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+1512C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861163 | ||||||
| chr4:25861359
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.162+1316T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861359 | ||||||
| chr4:25861498
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.162+1177A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861498 | ||||||
| chr4:25861515
|
A | T | 1 | a0001c0001t0002g0289 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.162+1160T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861515 | ||||||
| chr4:25861605
|
A | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.162+1070T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861605 | ||||||
| chr4:25861630
|
C | CT | 116 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0035others(113): Show | 116 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.162+1044dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861630 | ||||||
| chr4:25861630
|
C | CTT | 9 | a0001c0001t0001g0030a0001c0001t0001g0175a0001c0001t0002g0174others(6): Show | 9 | HG02083.hp2 HG02965.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+1043_162+1044d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861630 | ||||||
| chr4:25861630
|
CT | C | 30 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0293others(27): Show | 32 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.162+1044delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861630 | ||||||
| chr4:25861753
|
G | T | 147 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(144): Show | 148 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.162+922C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861753 | ||||||
| chr4:25861760
|
A | T | 9 | a0001c0011t0003g0172a0004c0007t0001g0164a0004c0007t0001g0165others(6): Show | 9 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+915T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861760 | ||||||
| chr4:25861837
|
C | T | 1 | a0001c0010t0002g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.162+838G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861837 | ||||||
| chr4:25861916
|
G | T | 166 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0019others(163): Show | 167 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.162+759C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861916 | ||||||
| chr4:25861940
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+735G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861940 | ||||||
| chr4:25862094
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0011g0004a0001c0001t0011g0005 | 3 | HG03654.hp1 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.162+581G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862094 | ||||||
| chr4:25862275
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.162+400C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862275 | ||||||
| chr4:25862308
|
G | C | 9 | a0001c0011t0003g0172a0004c0007t0001g0164a0004c0007t0001g0165others(6): Show | 9 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+367C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862308 | ||||||
| chr4:25862384
|
C | A | 133 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0184others(130): Show | 133 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(130): Show |
intron_variant | MODIFIER | c.162+291G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862384 | ||||||
| chr4:25862462
|
G | A | 10 | a0001c0001t0001g0293a0001c0001t0001g0296a0001c0001t0002g0294others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.162+213C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862462 |