| geneid | 57606 |
|---|---|
| ensemblid | ENSG00000109171.15 |
| hgncid | 29282 |
| symbol | SLAIN2 |
| name | SLAIN motif family member 2 |
| refseq_nuc | NM_020846.2 |
| refseq_prot | NP_065897.1 |
| ensembl_nuc | ENST00000264313.11 |
| ensembl_prot | ENSP00000264313.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 48341529 |
| end | 48426201 |
| strand | + |
| ver | v1.2 |
| region | chr4:48341529-48426201 |
| region5000 | chr4:48336529-48431201 |
| regionname0 | SLAIN2_chr4_48341529_48426201 |
| regionname5000 | SLAIN2_chr4_48336529_48431201 |
| 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 | 581 | 342 | 83 | 60 | 139 | 18 | 40 | 114 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0002 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0003 | 0/0 | 581 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0004 | 0/0 | 581 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0005 | 0/0 | 350 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0006 | 0/0 | 581 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0007 | 0/0 | 575 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| 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 | 1746 | 312 | 64 | 56 | 138 | 16 | 36 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0002 | 0/0 | 1746 | 15 | 4 | 4 | 1 | 2 | 4 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0003 | 0/0 | 1746 | 11 | 11 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0004 | 0/0 | 1746 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0005 | 0/0 | 1728 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0006 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0007 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0008 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0009 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0010 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| c0011 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4336 | 146 | 37 | 24 | 64 | 9 | 10 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0002 | 0/0 | 4335 | 77 | 19 | 18 | 24 | 3 | 13 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0003 | 0/0 | 4336 | 41 | 2 | 11 | 16 | 4 | 8 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0004 | 0/0 | 4335 | 26 | 3 | 1 | 19 | 0 | 3 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0005 | 0/0 | 4335 | 9 | 3 | 2 | 0 | 2 | 2 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0006 | 0/0 | 4331 | 8 | 8 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0007 | 0/0 | 4336 | 4 | 0 | 0 | 4 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0008 | 0/0 | 4336 | 4 | 0 | 4 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0009 | 0/0 | 4334 | 4 | 0 | 2 | 0 | 0 | 2 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0010 | 0/0 | 4336 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0011 | 0/0 | 4336 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0012 | 0/0 | 4331 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0013 | 0/0 | 4335 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0014 | 0/0 | 4331 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0015 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0016 | 0/0 | 4336 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0017 | 0/0 | 4335 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0018 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0019 | 0/0 | 4335 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0020 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0021 | 0/0 | 4335 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0022 | 0/0 | 4337 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0023 | 0/0 | 4336 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0024 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0025 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0026 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0027 | 0/0 | 4336 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0028 | 0/0 | 4335 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0029 | 0/0 | 4334 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0030 | 0/0 | 4334 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0031 | 0/0 | 4334 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0032 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0033 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| t0034 | 0/0 | 4336 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| 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 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| 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 | 1746 | 312 | 64 | 56 | 138 | 16 | 36 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0002 | 0/0 | 1746 | 15 | 4 | 4 | 1 | 2 | 4 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0003 | 0/0 | 1746 | 11 | 11 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0004 | 0/0 | 1746 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0006 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0002c0011 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0003c0010 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0004c0009 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0005c0007 | 0/0 | 1746 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0006c0008 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0007c0005 | 0/0 | 1728 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6081 | 142 | 35 | 22 | 64 | 9 | 10 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0002 | 0/0 | 6080 | 72 | 16 | 16 | 24 | 3 | 13 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0003 | 0/0 | 6081 | 41 | 2 | 11 | 16 | 4 | 8 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0004 | 0/0 | 6080 | 26 | 3 | 1 | 19 | 0 | 3 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0007 | 0/0 | 6081 | 4 | 0 | 0 | 4 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0008 | 0/0 | 6081 | 4 | 0 | 4 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0010 | 0/0 | 6081 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0011 | 0/0 | 6081 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0013 | 0/0 | 6080 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0015 | 0/0 | 6080 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0016 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0017 | 0/0 | 6080 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0018 | 0/0 | 6080 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0019 | 0/0 | 6080 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0021 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0022 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0023 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0024 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0025 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0026 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0027 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0028 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0029 | 0/0 | 6079 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0032 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0033 | 0/0 | 6080 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0001t0034 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0002t0005 | 0/0 | 6080 | 9 | 3 | 2 | 0 | 2 | 2 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0002t0009 | 0/0 | 6079 | 4 | 0 | 2 | 0 | 0 | 2 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0002t0030 | 0/0 | 6079 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0002t0031 | 0/0 | 6079 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0003t0006 | 0/0 | 6076 | 8 | 8 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0003t0012 | 0/0 | 6076 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0003t0014 | 0/0 | 6076 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0004t0002 | 0/0 | 6080 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0001c0006t0001 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0002c0011t0020 | 0/0 | 6080 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0003c0010t0001 | 0/0 | 6081 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0004c0009t0002 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0005c0007t0002 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0006c0008t0001 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| a0007c0005t0001 | 0/0 | 6063 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | copy fasta | chr4 | 48336529 | 48431201 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0007g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0007g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0007g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0007g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0008g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0010g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0013g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0013g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0015g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0016g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0017g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0018g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0019g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0021g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0022g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0023g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0024g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0025g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0026g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0027g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0028g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0029g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0032g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0033g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0034g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0009g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0009g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0009g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0009g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0030g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0031g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0012g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0004t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0004t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0002c0011t0020g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0003c0010t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0004c0009t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0005c0007t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0006c0008t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0007c0005t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0208 | EUR | GBR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | GBR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0215 | EUR | FIN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0165 | EUR | FIN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00408 | hp1 | a0001 | c0001 | t0033 | g0294 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00738 | hp1 | a0003 | c0010 | t0001 | g0136 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0332 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00741 | hp2 | a0001 | c0002 | t0009 | g0204 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01069 | hp2 | a0001 | c0002 | t0005 | g0005 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01074 | hp1 | a0001 | c0002 | t0009 | g0171 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01099 | hp1 | a0001 | c0001 | t0028 | g0274 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0310 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01109 | hp1 | a0005 | c0007 | t0002 | g0309 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0005 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0145 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0328 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0142 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0229 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0182 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0301 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01891 | hp2 | a0001 | c0003 | t0014 | g0153 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0144 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01978 | hp2 | a0004 | c0009 | t0002 | g0331 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0146 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02004 | hp1 | a0001 | c0001 | t0021 | g0242 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0088 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02040 | hp1 | a0002 | c0011 | t0020 | g0263 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0176 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02056 | hp2 | a0001 | c0001 | t0013 | g0293 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0327 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02145 | hp2 | a0001 | c0003 | t0006 | g0220 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0329 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02148 | hp2 | a0007 | c0005 | t0001 | g0104 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02155 | hp2 | a0001 | c0001 | t0013 | g0245 | EAS | CDX | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0339 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02258 | hp1 | a0001 | c0001 | t0029 | g0163 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02258 | hp2 | a0001 | c0003 | t0006 | g0029 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0336 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0237 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02451 | hp2 | a0001 | c0003 | t0006 | g0218 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02523 | hp1 | a0001 | c0002 | t0031 | g0178 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0278 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02615 | hp1 | a0001 | c0001 | t0016 | g0340 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02615 | hp2 | a0001 | c0003 | t0012 | g0221 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02630 | hp2 | a0001 | c0001 | t0023 | g0031 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0299 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0334 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0027 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02895 | hp1 | a0006 | c0008 | t0001 | g0120 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02922 | hp2 | a0001 | c0003 | t0006 | g0028 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02965 | hp2 | a0001 | c0006 | t0001 | g0096 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03017 | hp1 | a0001 | c0001 | t0017 | g0241 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0187 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0173 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03098 | hp1 | a0001 | c0003 | t0006 | g0219 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03139 | hp1 | a0001 | c0004 | t0002 | g0236 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03139 | hp2 | a0001 | c0001 | t0027 | g0181 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03195 | hp2 | a0001 | c0004 | t0002 | g0238 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0279 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03225 | hp2 | a0001 | c0001 | t0015 | g0303 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03453 | hp1 | a0001 | c0003 | t0006 | g0223 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03453 | hp2 | a0001 | c0001 | t0018 | g0290 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0203 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0170 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03492 | hp2 | a0001 | c0002 | t0005 | g0177 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03540 | hp1 | a0001 | c0003 | t0012 | g0222 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0017 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0210 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0319 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03831 | hp2 | a0001 | c0001 | t0019 | g0312 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0262 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03927 | hp2 | a0001 | c0002 | t0009 | g0172 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0314 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04184 | hp1 | a0001 | c0002 | t0009 | g0179 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0248 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0198 | SAS | STU | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | STU | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0318 | SAS | STU | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | CHB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | CHB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18939 | hp1 | a0001 | c0001 | t0025 | g0043 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18964 | hp1 | a0001 | c0001 | t0024 | g0010 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0330 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0321 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19005 | hp2 | a0001 | c0001 | t0026 | g0070 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19030 | hp1 | a0001 | c0002 | t0030 | g0205 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0032 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19056 | hp2 | a0001 | c0001 | t0022 | g0115 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19064 | hp1 | a0001 | c0001 | t0034 | g0183 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19078 | hp2 | a0001 | c0001 | t0007 | g0337 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19079 | hp2 | a0001 | c0001 | t0032 | g0057 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19083 | hp2 | a0001 | c0001 | t0007 | g0273 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19086 | hp2 | a0001 | c0001 | t0010 | g0089 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0335 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0180 | AFR | ASW | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ASW | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20752 | hp1 | a0001 | c0002 | t0005 | g0175 | EUR | TSI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20805 | hp2 | a0001 | c0002 | t0005 | g0174 | EUR | TSI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | GIH | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0297 | SAS | GIH | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02559 | hp2 | a0001 | c0003 | t0006 | g0030 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | USA | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | USA | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | USA | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | USA | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0148 | REF | REF | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0025 | REF | REF | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48341909
|
C | T | 1 | a0002 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.170C>T | p.Pro57Leu | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 381/6081 | 170/1746 | 57/581 | chr4 | 48341909 | ||
| chr4:48341960
|
AGTCGGGC others(11): Show |
A | 1 | a0007 | 1 | HG02148.hp2 | conservative_inframe_deletion | MODERATE | c.229_246delGGCGGGCC others(10): Show |
p.Gly77_Gly82del | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 440/6081 | 229/1746 | 77/581 | INFO_REALIGN_3_PRIME | chr4 | 48341960 | |
| chr4:48342076
|
C | G | 1 | a0003 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.337C>G | p.Arg113Gly | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 548/6081 | 337/1746 | 113/581 | chr4 | 48342076 | ||
| chr4:48379710
|
A | G | 1 | a0004 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.724A>G | p.Arg242Gly | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/8 | 935/6081 | 724/1746 | 242/581 | chr4 | 48379710 | ||
| chr4:48379782
|
A | G | 1 | a0006 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.796A>G | p.Ile266Val | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/8 | 1007/6081 | 796/1746 | 266/581 | chr4 | 48379782 | ||
| chr4:48382756
|
C | T | 1 | a0005 | 1 | HG01109.hp1 | stop_gained | HIGH | c.1051C>T | p.Arg351* | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/8 | 1262/6081 | 1051/1746 | 351/581 | chr4 | 48382756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48341751
|
T | C | 1 | a0001c0004 | 3 | HG02451.hp1 HG03139.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.12T>C | p.Val4Val | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 223/6081 | 12/1746 | 4/581 | chr4 | 48341751 | ||
| chr4:48342072
|
G | C | 1 | a0001c0006 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.333G>C | p.Pro111Pro | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 544/6081 | 333/1746 | 111/581 | chr4 | 48342072 | ||
| chr4:48382602
|
G | A | 1 | a0001c0003 | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
synonymous_variant | LOW | c.897G>A | p.Arg299Arg | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/8 | 1108/6081 | 897/1746 | 299/581 | chr4 | 48382602 | ||
| chr4:48422041
|
C | T | 1 | a0001c0002 | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
synonymous_variant | LOW | c.1710C>T | p.Ser570Ser | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1921/6081 | 1710/1746 | 570/581 | chr4 | 48422041 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48341533
|
C | T | 2 | a0001c0001t0003a0001c0001t0034 | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-207C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 207 | chr4 | 48341533 | |||||
| chr4:48341633
|
G | C | 1 | a0001c0003t0014 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-107G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 107 | chr4 | 48341633 | |||||
| chr4:48341671
|
C | T | 2 | a0001c0001t0013a0001c0001t0033 | 3 | HG00408.hp1 HG02056.hp2 HG02155.hp2 |
5_prime_UTR_variant | MODIFIER | c.-69C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 69 | chr4 | 48341671 | |||||
| chr4:48341676
|
G | A | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(12): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
5_prime_UTR_variant | MODIFIER | c.-64G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 64 | chr4 | 48341676 | |||||
| chr4:48341685
|
C | T | 1 | a0001c0001t0032 | 1 | NA19079.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 55 | chr4 | 48341685 | |||||
| chr4:48422418
|
A | G | 1 | a0001c0001t0034 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 341 | chr4 | 48422418 | |||||
| chr4:48422634
|
T | A | 1 | a0001c0001t0033 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*557T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 557 | chr4 | 48422634 | |||||
| chr4:48423113
|
C | G | 1 | a0001c0002t0031 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1036C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1036 | chr4 | 48423113 | |||||
| chr4:48423179
|
G | C | 1 | a0001c0001t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1102G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1102 | chr4 | 48423179 | |||||
| chr4:48423191
|
A | T | 1 | a0001c0002t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1114A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1114 | chr4 | 48423191 | |||||
| chr4:48423275
|
TA | T | 14 | a0001c0001t0002a0001c0001t0004a0001c0001t0013others(11): Show | 113 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1208delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1208 | INFO_REALIGN_3_PRIME | chr4 | 48423275 | ||||
| chr4:48423275
|
TAA | T | 5 | a0001c0001t0029a0001c0002t0005a0001c0002t0009others(2): Show | 16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1207_*1208delAA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1207 | INFO_REALIGN_3_PRIME | chr4 | 48423275 | ||||
| chr4:48423275
|
TAAAAA | T | 3 | a0001c0003t0006a0001c0003t0012a0001c0003t0014 | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1204_*1208delAAAA others(1): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1204 | INFO_REALIGN_3_PRIME | chr4 | 48423275 | ||||
| chr4:48423338
|
T | G | 1 | a0001c0002t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1261T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1261 | chr4 | 48423338 | |||||
| chr4:48423431
|
G | T | 1 | a0001c0001t0021 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1354 | chr4 | 48423431 | |||||
| chr4:48423461
|
A | C | 1 | a0002c0011t0020 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1384A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1384 | chr4 | 48423461 | |||||
| chr4:48423670
|
C | G | 1 | a0001c0001t0019 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1593C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1593 | chr4 | 48423670 | |||||
| chr4:48424049
|
A | T | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(12): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1972A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1972 | chr4 | 48424049 | |||||
| chr4:48424470
|
A | G | 1 | a0001c0001t0027 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2393A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2393 | chr4 | 48424470 | |||||
| chr4:48424565
|
A | G | 1 | a0001c0001t0018 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2488A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2488 | chr4 | 48424565 | |||||
| chr4:48424585
|
T | G | 2 | a0001c0001t0008a0001c0001t0022 | 5 | HG01256.hp2 HG01496.hp2 HG01943.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2508T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2508 | chr4 | 48424585 | |||||
| chr4:48424748
|
C | T | 1 | a0001c0001t0026 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2671C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2671 | chr4 | 48424748 | |||||
| chr4:48424766
|
T | TA | 2 | a0001c0001t0022a0001c0002t0005 | 10 | HG01069.hp2 HG01109.hp2 HG02055.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2700dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2701 | INFO_REALIGN_3_PRIME | chr4 | 48424766 | ||||
| chr4:48424929
|
G | A | 3 | a0001c0003t0006a0001c0003t0012a0001c0003t0014 | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2852G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2852 | chr4 | 48424929 | |||||
| chr4:48424998
|
A | G | 1 | a0001c0001t0025 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2921A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2921 | chr4 | 48424998 | |||||
| chr4:48425243
|
C | T | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(23): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*3166C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3166 | chr4 | 48425243 | |||||
| chr4:48425273
|
A | G | 1 | a0001c0001t0004 | 26 | HG00609.hp1 HG01099.hp2 HG02074.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3196A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3196 | chr4 | 48425273 | |||||
| chr4:48425442
|
C | T | 1 | a0001c0001t0024 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3365C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3365 | chr4 | 48425442 | |||||
| chr4:48425452
|
T | C | 1 | a0001c0001t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3375T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3375 | chr4 | 48425452 | |||||
| chr4:48425605
|
A | T | 1 | a0001c0001t0023 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3528A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3528 | chr4 | 48425605 | |||||
| chr4:48425612
|
A | G | 3 | a0001c0002t0005a0001c0002t0009a0001c0002t0031 | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3535A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3535 | chr4 | 48425612 | |||||
| chr4:48425702
|
C | T | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(12): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*3625C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3625 | chr4 | 48425702 | |||||
| chr4:48425756
|
G | A | 15 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(12): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*3679G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3679 | chr4 | 48425756 | |||||
| chr4:48425860
|
G | A | 1 | a0001c0001t0010 | 2 | HG02015.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3783G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3783 | chr4 | 48425860 | |||||
| chr4:48425974
|
A | G | 1 | a0001c0001t0011 | 2 | HG02809.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3897A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3897 | chr4 | 48425974 | |||||
| chr4:48426009
|
C | G | 1 | a0001c0001t0017 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3932C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3932 | chr4 | 48426009 | |||||
| chr4:48426075
|
C | T | 1 | a0001c0003t0012 | 2 | HG02615.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3998C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3998 | chr4 | 48426075 | |||||
| chr4:48426084
|
C | T | 3 | a0001c0002t0005a0001c0002t0009a0001c0002t0031 | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4007C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 4007 | chr4 | 48426084 | |||||
| chr4:48426136
|
G | A | 1 | a0001c0002t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4059G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 4059 | chr4 | 48426136 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48342137
|
G | T | 116 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(113): Show | 118 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.389+9G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342137 | ||||||
| chr4:48342182
|
A | T | 1 | a0001c0001t0001g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.389+54A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342182 | ||||||
| chr4:48342313
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.389+185C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342313 | ||||||
| chr4:48342340
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.389+212C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342340 | ||||||
| chr4:48342592
|
G | T | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+464G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342592 | ||||||
| chr4:48342593
|
C | T | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+465C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342593 | ||||||
| chr4:48342711
|
C | CT | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0033others(106): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.389+607dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | |||||
| chr4:48342711
|
C | CTT | 28 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(25): Show | 28 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.389+606_389+607dup others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | |||||
| chr4:48342711
|
C | CTTT | 89 | a0001c0001t0001g0162a0001c0001t0001g0224a0001c0001t0002g0006others(86): Show | 91 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.389+605_389+607dup others(3): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | |||||
| chr4:48342711
|
C | CTTTT | 44 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(41): Show | 46 | HG00323.hp2 HG00733.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.389+604_389+607dup others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | |||||
| chr4:48342711
|
C | CTTTTT | 27 | a0001c0001t0002g0339a0001c0001t0003g0184a0001c0001t0003g0185others(24): Show | 27 | HG00738.hp2 HG00741.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.389+603_389+607dup others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | |||||
| chr4:48342711
|
C | CTTTTTT | 11 | a0001c0001t0003g0207a0001c0001t0003g0208a0001c0001t0003g0209others(8): Show | 11 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.389+602_389+607dup others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | |||||
| chr4:48342711
|
C | CTTTTTTT others(5): Show |
1 | a0001c0003t0006g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.389+596_389+607dup others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | |||||
| chr4:48342711
|
C | CTTTTTTT others(6): Show |
4 | a0001c0003t0006g0219a0001c0003t0006g0220a0001c0003t0012g0221others(1): Show | 4 | HG02145.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.389+595_389+607dup others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | |||||
| chr4:48342711
|
C | CTTTTTTT others(7): Show |
1 | a0001c0003t0006g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+594_389+607dup others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | |||||
| chr4:48342766
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+638C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342766 | ||||||
| chr4:48342772
|
C | G | 1 | a0001c0001t0007g0337 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.389+644C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342772 | ||||||
| chr4:48342774
|
G | A | 37 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(34): Show | 38 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.389+646G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342774 | ||||||
| chr4:48342913
|
A | G | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.389+785A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342913 | ||||||
| chr4:48342999
|
C | T | 1 | a0001c0003t0006g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.389+871C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342999 | ||||||
| chr4:48343118
|
T | C | 9 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.389+990T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343118 | ||||||
| chr4:48343213
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.389+1085A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343213 | ||||||
| chr4:48343434
|
A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+1306A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343434 | ||||||
| chr4:48343734
|
T | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0034others(10): Show | 14 | HG02074.hp2 NA18939.hp1 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.389+1606T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343734 | ||||||
| chr4:48343887
|
T | A | 2 | a0001c0001t0003g0202a0001c0001t0003g0217 | 2 | NA18943.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.389+1759T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343887 | ||||||
| chr4:48343989
|
C | T | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.389+1861C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343989 | ||||||
| chr4:48344085
|
G | GT | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.389+1960dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48344085 | |||||
| chr4:48344266
|
T | A | 12 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(9): Show | 13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.389+2138T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344266 | ||||||
| chr4:48344511
|
A | C | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.389+2383A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344511 | ||||||
| chr4:48344564
|
G | A | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+2436G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344564 | ||||||
| chr4:48344686
|
T | A | 1 | a0001c0001t0001g0044 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.389+2558T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344686 | ||||||
| chr4:48344721
|
T | C | 3 | a0001c0001t0004g0231a0001c0001t0004g0232a0001c0001t0004g0233 | 3 | NA18946.hp2 NA19012.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.389+2593T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344721 | ||||||
| chr4:48344802
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.389+2674C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344802 | ||||||
| chr4:48344807
|
A | T | 1 | a0001c0001t0001g0137 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.389+2679A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344807 | ||||||
| chr4:48344868
|
G | T | 108 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(105): Show | 110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.389+2740G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344868 | ||||||
| chr4:48344929
|
A | G | 1 | a0003c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.389+2801A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344929 | ||||||
| chr4:48344976
|
T | A | 170 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+2848T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344976 | ||||||
| chr4:48345284
|
C | G | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.389+3156C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345284 | ||||||
| chr4:48345300
|
C | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.389+3172C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345300 | ||||||
| chr4:48345369
|
G | T | 1 | a0001c0001t0001g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.389+3241G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345369 | ||||||
| chr4:48345407
|
T | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+3279T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345407 | ||||||
| chr4:48345414
|
C | T | 13 | a0001c0001t0029g0163a0001c0002t0030g0205a0001c0003t0006g0028others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.389+3286C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345414 | ||||||
| chr4:48345580
|
C | A | 2 | a0001c0001t0002g0239a0001c0001t0002g0240 | 2 | HG00597.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.389+3452C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345580 | ||||||
| chr4:48345596
|
A | G | 10 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.389+3468A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345596 | ||||||
| chr4:48345729
|
TGTTA | T | 9 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(6): Show | 9 | HG01070.hp1 HG01433.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+3605_389+3608d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48345729 | |||||
| chr4:48345746
|
A | G | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.389+3618A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345746 | ||||||
| chr4:48345921
|
A | T | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+3793A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345921 | ||||||
| chr4:48345959
|
C | A | 1 | a0001c0001t0003g0164 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.389+3831C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345959 | ||||||
| chr4:48345990
|
T | TGAAA | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(311): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.389+3864_389+3865i others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48345990 | |||||
| chr4:48346009
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+3881G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48346009 | ||||||
| chr4:48346731
|
G | A | 1 | a0001c0001t0017g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.389+4603G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48346731 | ||||||
| chr4:48346797
|
GAATCAGA others(456): Show |
G | 3 | a0001c0004t0002g0236a0001c0004t0002g0237a0001c0004t0002g0238 | 3 | HG02451.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.389+4673_389+5135d others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48346797 | |||||
| chr4:48346835
|
C | CT | 17 | a0001c0001t0001g0116a0001c0001t0001g0123a0001c0001t0001g0157others(14): Show | 17 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.389+4727dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48346835 | |||||
| chr4:48346835
|
CT | C | 116 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0046others(113): Show | 118 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.389+4727delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48346835 | |||||
| chr4:48346835
|
CTT | C | 15 | a0001c0001t0002g0228a0001c0001t0002g0243a0001c0001t0002g0244others(12): Show | 15 | HG01891.hp2 HG01975.hp2 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.389+4726_389+4727d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48346835 | |||||
| chr4:48346855
|
T | A | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.389+4727T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48346855 | ||||||
| chr4:48346942
|
A | G | 13 | a0001c0001t0029g0163a0001c0002t0030g0205a0001c0003t0006g0028others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.389+4814A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48346942 | ||||||
| chr4:48347252
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+5124G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347252 | ||||||
| chr4:48347315
|
G | A | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.389+5187G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347315 | ||||||
| chr4:48347344
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+5216C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347344 | ||||||
| chr4:48347390
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+5262C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347390 | ||||||
| chr4:48347397
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+5269C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347397 | ||||||
| chr4:48347427
|
T | G | 3 | a0001c0001t0003g0186a0001c0001t0003g0201a0001c0001t0034g0183 | 3 | NA18963.hp2 NA18992.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.389+5299T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347427 | ||||||
| chr4:48347449
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.389+5321A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347449 | ||||||
| chr4:48347468
|
C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+5340C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347468 | ||||||
| chr4:48347635
|
A | G | 1 | a0001c0001t0002g0244 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.389+5507A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347635 | ||||||
| chr4:48347673
|
A | G | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.389+5545A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347673 | ||||||
| chr4:48347694
|
A | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(4): Show | 7 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+5566A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347694 | ||||||
| chr4:48347761
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+5633G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347761 | ||||||
| chr4:48347781
|
G | A | 1 | a0001c0001t0013g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.389+5653G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347781 | ||||||
| chr4:48347782
|
C | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+5654C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347782 | ||||||
| chr4:48347897
|
A | T | 5 | a0001c0002t0009g0171a0001c0002t0009g0172a0001c0002t0009g0179others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.389+5769A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347897 | ||||||
| chr4:48347925
|
T | G | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+5797T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347925 | ||||||
| chr4:48347962
|
A | G | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.389+5834A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347962 | ||||||
| chr4:48348022
|
A | C | 1 | a0001c0001t0011g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.389+5894A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348022 | ||||||
| chr4:48348025
|
A | C | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.389+5897A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348025 | ||||||
| chr4:48348029
|
A | T | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+5901A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348029 | ||||||
| chr4:48348044
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.389+5916C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348044 | ||||||
| chr4:48348117
|
CT | C | 10 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.389+5990delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348117 | ||||||
| chr4:48348137
|
T | C | 1 | a0001c0001t0013g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.389+6009T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348137 | ||||||
| chr4:48348155
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.389+6027G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348155 | ||||||
| chr4:48348183
|
A | C | 1 | a0001c0001t0002g0336 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.389+6055A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348183 | ||||||
| chr4:48348237
|
T | A | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.389+6109T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348237 | ||||||
| chr4:48348247
|
T | TAAAAA | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+6120_389+6121i others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348247 | |||||
| chr4:48348252
|
TA | T | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+6131delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348252 | |||||
| chr4:48348560
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.389+6432G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348560 | ||||||
| chr4:48348648
|
C | G | 1 | a0001c0001t0003g0200 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.389+6520C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348648 | ||||||
| chr4:48348689
|
C | CA | 45 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(42): Show | 46 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.389+6578dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348689 | |||||
| chr4:48348689
|
C | CAA | 73 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(70): Show | 74 | HG00597.hp2 HG00609.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.389+6577_389+6578d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348689 | |||||
| chr4:48348689
|
C | CAAA | 11 | a0001c0001t0002g0227a0001c0001t0002g0234a0001c0001t0002g0246others(8): Show | 11 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.389+6576_389+6578d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348689 | |||||
| chr4:48348704
|
AAAG | A | 9 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.389+6581_389+6583d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348704 | |||||
| chr4:48348740
|
G | A | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.389+6612G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348740 | ||||||
| chr4:48348770
|
C | T | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+6642C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348770 | ||||||
| chr4:48348771
|
A | G | 15 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(12): Show | 16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.389+6643A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348771 | ||||||
| chr4:48348827
|
C | T | 10 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.389+6699C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348827 | ||||||
| chr4:48348828
|
C | T | 1 | a0001c0001t0003g0200 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.389+6700C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348828 | ||||||
| chr4:48348883
|
A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+6755A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348883 | ||||||
| chr4:48348973
|
C | A | 5 | a0001c0001t0002g0292a0001c0001t0007g0330a0001c0001t0013g0245others(2): Show | 5 | HG00408.hp1 HG02056.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.389+6845C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348973 | ||||||
| chr4:48348996
|
A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+6868A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348996 | ||||||
| chr4:48349047
|
T | C | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+6919T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349047 | ||||||
| chr4:48349079
|
T | C | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+6951T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349079 | ||||||
| chr4:48349551
|
C | G | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.389+7423C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349551 | ||||||
| chr4:48349561
|
A | G | 1 | a0001c0001t0002g0250 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.389+7433A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349561 | ||||||
| chr4:48349623
|
C | T | 6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+7495C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349623 | ||||||
| chr4:48349964
|
C | CA | 14 | a0001c0001t0001g0139a0001c0002t0005g0005a0001c0002t0005g0173others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.389+7844dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48349964 | |||||
| chr4:48350213
|
G | C | 1 | a0004c0009t0002g0331 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.389+8085G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350213 | ||||||
| chr4:48350219
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.389+8091G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350219 | ||||||
| chr4:48350315
|
A | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0109 | 2 | HG00558.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.389+8187A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350315 | ||||||
| chr4:48350511
|
G | A | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.389+8383G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350511 | ||||||
| chr4:48350906
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.389+8778A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350906 | ||||||
| chr4:48351016
|
A | G | 2 | a0001c0001t0002g0230a0001c0001t0002g0291 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.389+8888A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351016 | ||||||
| chr4:48351268
|
A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+9140A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351268 | ||||||
| chr4:48351303
|
A | G | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+9175A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351303 | ||||||
| chr4:48351325
|
G | A | 71 | a0001c0001t0002g0006a0001c0001t0002g0228a0001c0001t0002g0239others(68): Show | 72 | HG00597.hp2 HG00609.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.389+9197G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351325 | ||||||
| chr4:48351462
|
T | C | 1 | a0001c0001t0004g0251 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.389+9334T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351462 | ||||||
| chr4:48351464
|
A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+9336A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351464 | ||||||
| chr4:48351669
|
A | T | 170 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+9541A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351669 | ||||||
| chr4:48351697
|
C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+9569C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351697 | ||||||
| chr4:48351701
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.389+9573C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351701 | ||||||
| chr4:48351740
|
G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+9612G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351740 | ||||||
| chr4:48351754
|
G | A | 1 | a0001c0001t0003g0186 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.389+9626G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351754 | ||||||
| chr4:48351816
|
T | C | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+9688T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351816 | ||||||
| chr4:48351861
|
T | C | 1 | a0001c0001t0004g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.389+9733T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351861 | ||||||
| chr4:48351880
|
C | T | 6 | a0001c0002t0005g0005a0001c0002t0005g0174a0001c0002t0005g0175others(3): Show | 7 | HG01069.hp2 HG01109.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+9752C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351880 | ||||||
| chr4:48351955
|
G | A | 7 | a0001c0001t0002g0227a0001c0001t0002g0234a0001c0001t0002g0235others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+9827G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351955 | ||||||
| chr4:48352040
|
C | T | 170 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+9912C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352040 | ||||||
| chr4:48352049
|
T | C | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+9921T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352049 | ||||||
| chr4:48352112
|
A | AT | 108 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(105): Show | 110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.389+9985dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48352112 | |||||
| chr4:48352114
|
G | T | 108 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(105): Show | 110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.389+9986G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352114 | ||||||
| chr4:48352115
|
C | T | 108 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(105): Show | 110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.389+9987C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352115 | ||||||
| chr4:48352116
|
T | G | 7 | a0001c0001t0002g0227a0001c0001t0002g0234a0001c0001t0002g0235others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+9988T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352116 | ||||||
| chr4:48352269
|
A | G | 1 | a0001c0001t0002g0288 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.389+10141A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352269 | ||||||
| chr4:48352328
|
T | C | 6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+10200T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352328 | ||||||
| chr4:48352405
|
A | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.389+10277A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352405 | ||||||
| chr4:48352498
|
G | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+10370G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352498 | ||||||
| chr4:48352542
|
T | A | 2 | a0001c0001t0003g0187a0001c0001t0003g0210 | 2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.389+10414T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352542 | ||||||
| chr4:48352604
|
T | C | 182 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(179): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.389+10476T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352604 | ||||||
| chr4:48352648
|
A | T | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+10520A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352648 | ||||||
| chr4:48352664
|
A | C | 2 | a0001c0003t0012g0221a0001c0003t0012g0222 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.389+10536A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352664 | ||||||
| chr4:48352680
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.389+10552G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352680 | ||||||
| chr4:48353102
|
A | T | 1 | a0001c0001t0002g0287 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.389+10974A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353102 | ||||||
| chr4:48353172
|
G | A | 4 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0316others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.389+11044G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353172 | ||||||
| chr4:48353387
|
T | C | 2 | a0001c0001t0002g0292a0001c0001t0007g0330 | 2 | NA18977.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.389+11259T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353387 | ||||||
| chr4:48353427
|
T | TCATGGTC others(242): Show |
1 | a0001c0002t0005g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.389+11312_389+1131 others(253): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48353427 | |||||
| chr4:48353527
|
G | A | 193 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.389+11399G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353527 | ||||||
| chr4:48353587
|
CAG | C | 9 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.389+11461_389+1146 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48353587 | |||||
| chr4:48353734
|
A | G | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.389+11606A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353734 | ||||||
| chr4:48353816
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+11688G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353816 | ||||||
| chr4:48353931
|
A | G | 1 | a0001c0001t0002g0314 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.389+11803A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353931 | ||||||
| chr4:48353942
|
C | T | 193 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.389+11814C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353942 | ||||||
| chr4:48354013
|
C | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+11885C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354013 | ||||||
| chr4:48354046
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+11918C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354046 | ||||||
| chr4:48354079
|
T | G | 3 | a0001c0001t0003g0207a0001c0001t0003g0208a0001c0001t0003g0209 | 3 | HG00099.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.389+11951T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354079 | ||||||
| chr4:48354130
|
T | G | 1 | a0001c0001t0003g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.389+12002T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354130 | ||||||
| chr4:48354136
|
TAA | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+12017_389+1201 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48354136 | |||||
| chr4:48354206
|
T | C | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+12078T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354206 | ||||||
| chr4:48354298
|
A | G | 1 | a0001c0001t0034g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.389+12170A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354298 | ||||||
| chr4:48354316
|
G | A | 170 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+12188G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354316 | ||||||
| chr4:48354461
|
C | T | 177 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.389+12333C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354461 | ||||||
| chr4:48354466
|
AT | A | 170 | a0001c0001t0001g0058a0001c0001t0001g0154a0001c0001t0001g0155others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+12349delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48354466 | |||||
| chr4:48354472
|
T | C | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+12344T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354472 | ||||||
| chr4:48354476
|
T | C | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+12348T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354476 | ||||||
| chr4:48354477
|
T | C | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.389+12349T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354477 | ||||||
| chr4:48354552
|
T | C | 1 | a0001c0001t0003g0211 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.389+12424T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354552 | ||||||
| chr4:48354612
|
A | G | 1 | a0001c0001t0019g0312 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.389+12484A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354612 | ||||||
| chr4:48354651
|
G | C | 2 | a0001c0001t0003g0187a0001c0001t0003g0210 | 2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.389+12523G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354651 | ||||||
| chr4:48354690
|
C | T | 1 | a0001c0002t0005g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.389+12562C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354690 | ||||||
| chr4:48354725
|
G | A | 192 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.389+12597G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354725 | ||||||
| chr4:48354734
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+12606G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354734 | ||||||
| chr4:48354760
|
A | G | 2 | a0001c0002t0005g0177a0001c0002t0005g0203 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.389+12632A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354760 | ||||||
| chr4:48354884
|
ATTTTC | A | 146 | a0001c0001t0002g0006a0001c0001t0002g0227a0001c0001t0002g0228others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.389+12771_389+1277 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48354884 | |||||
| chr4:48354895
|
TTTTC | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0243a0001c0001t0002g0305others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.389+12771_389+1277 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48354895 | |||||
| chr4:48354906
|
T | C | 11 | a0001c0001t0002g0007a0001c0001t0002g0243a0001c0001t0002g0305others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.389+12778T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354906 | ||||||
| chr4:48354907
|
C | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0243a0001c0001t0002g0305others(8): Show | 12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.389+12779C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354907 | ||||||
| chr4:48354990
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.389+12862C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354990 | ||||||
| chr4:48355016
|
G | A | 7 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(4): Show | 7 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+12888G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355016 | ||||||
| chr4:48355022
|
C | T | 1 | a0001c0003t0006g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.389+12894C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355022 | ||||||
| chr4:48355027
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+12899G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355027 | ||||||
| chr4:48355066
|
G | A | 10 | a0001c0002t0005g0005a0001c0002t0005g0174a0001c0002t0005g0175others(7): Show | 11 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.389+12938G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355066 | ||||||
| chr4:48355079
|
G | C | 11 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(8): Show | 12 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.389+12951G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355079 | ||||||
| chr4:48355088
|
G | C | 1 | a0001c0001t0004g0318 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.389+12960G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355088 | ||||||
| chr4:48355160
|
G | A | 2 | a0001c0003t0006g0032a0001c0003t0014g0153 | 2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.389+13032G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355160 | ||||||
| chr4:48355219
|
G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+13091G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355219 | ||||||
| chr4:48355272
|
C | T | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.389+13144C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355272 | ||||||
| chr4:48355510
|
A | G | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.389+13382A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355510 | ||||||
| chr4:48355607
|
G | C | 1 | a0001c0001t0002g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389+13479G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355607 | ||||||
| chr4:48355666
|
C | T | 2 | a0001c0001t0002g0285a0001c0001t0002g0286 | 2 | HG01928.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.389+13538C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355666 | ||||||
| chr4:48355717
|
T | A | 1 | a0001c0001t0003g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.389+13589T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355717 | ||||||
| chr4:48355718
|
C | A | 1 | a0001c0001t0003g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.389+13590C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355718 | ||||||
| chr4:48355736
|
C | T | 2 | a0001c0001t0001g0108a0001c0001t0002g0335 | 2 | NA19086.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.389+13608C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355736 | ||||||
| chr4:48356005
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-13844C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356005 | ||||||
| chr4:48356345
|
G | T | 1 | a0001c0003t0006g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.390-13504G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356345 | ||||||
| chr4:48356425
|
T | C | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390-13424T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356425 | ||||||
| chr4:48356434
|
CTGTACTA others(15): Show |
C | 1 | a0001c0001t0002g0284 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.390-13393_390-1337 others(26): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48356434 | |||||
| chr4:48356438
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.390-13411A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356438 | ||||||
| chr4:48356456
|
A | C | 2 | a0001c0001t0001g0160a0001c0001t0029g0163 | 2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.390-13393A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356456 | ||||||
| chr4:48356504
|
G | A | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390-13345G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356504 | ||||||
| chr4:48356703
|
T | C | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-13146T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356703 | ||||||
| chr4:48356710
|
T | G | 4 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(1): Show | 6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-13139T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356710 | ||||||
| chr4:48356743
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.390-13106C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356743 | ||||||
| chr4:48356793
|
C | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0116 | 2 | NA18946.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.390-13056C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356793 | ||||||
| chr4:48356979
|
C | T | 2 | a0001c0001t0001g0105a0007c0005t0001g0104 | 2 | HG02148.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.390-12870C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356979 | ||||||
| chr4:48356997
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-12852C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356997 | ||||||
| chr4:48357158
|
T | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-12691T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357158 | ||||||
| chr4:48357170
|
C | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-12679C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357170 | ||||||
| chr4:48357201
|
A | G | 1 | a0001c0001t0002g0304 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390-12648A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357201 | ||||||
| chr4:48357273
|
G | A | 1 | a0001c0001t0003g0182 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.390-12576G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357273 | ||||||
| chr4:48357306
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.390-12543A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357306 | ||||||
| chr4:48357375
|
CT | C | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-12463delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48357375 | |||||
| chr4:48357709
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-12140C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357709 | ||||||
| chr4:48357735
|
G | A | 170 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.390-12114G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357735 | ||||||
| chr4:48357744
|
A | G | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.390-12105A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357744 | ||||||
| chr4:48357755
|
A | G | 108 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(105): Show | 110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.390-12094A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357755 | ||||||
| chr4:48357888
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.390-11961A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357888 | ||||||
| chr4:48357998
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.390-11851C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357998 | ||||||
| chr4:48358267
|
A | G | 4 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0328others(1): Show | 4 | HG01358.hp1 HG01928.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-11582A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358267 | ||||||
| chr4:48358323
|
C | CT | 113 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(110): Show | 115 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.390-11513dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48358323 | |||||
| chr4:48358341
|
C | T | 2 | a0001c0001t0001g0044a0001c0002t0030g0205 | 2 | NA18998.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.390-11508C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358341 | ||||||
| chr4:48358353
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.390-11496C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358353 | ||||||
| chr4:48358380
|
C | T | 1 | a0001c0001t0004g0318 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.390-11469C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358380 | ||||||
| chr4:48358464
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.390-11385C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358464 | ||||||
| chr4:48358465
|
G | A | 1 | a0001c0001t0003g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.390-11384G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358465 | ||||||
| chr4:48358535
|
C | T | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.390-11314C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358535 | ||||||
| chr4:48358559
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.390-11290G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358559 | ||||||
| chr4:48358608
|
G | A | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.390-11241G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358608 | ||||||
| chr4:48358686
|
G | C | 1 | a0001c0001t0001g0059 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.390-11163G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358686 | ||||||
| chr4:48358728
|
A | AT | 109 | a0001c0001t0001g0102a0001c0001t0002g0006a0001c0001t0002g0007others(106): Show | 111 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.390-11112dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48358728 | |||||
| chr4:48358814
|
G | A | 108 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(105): Show | 110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.390-11035G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358814 | ||||||
| chr4:48358815
|
G | C | 1 | a0001c0001t0001g0060 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.390-11034G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358815 | ||||||
| chr4:48358920
|
A | C | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.390-10929A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358920 | ||||||
| chr4:48358922
|
T | C | 1 | a0001c0001t0003g0199 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.390-10927T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358922 | ||||||
| chr4:48358960
|
A | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-10889A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358960 | ||||||
| chr4:48359118
|
T | C | 1 | a0001c0001t0002g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.390-10731T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359118 | ||||||
| chr4:48359304
|
G | C | 1 | a0001c0001t0003g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.390-10545G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359304 | ||||||
| chr4:48359490
|
C | G | 116 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(113): Show | 118 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.390-10359C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359490 | ||||||
| chr4:48359709
|
T | C | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.390-10140T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359709 | ||||||
| chr4:48359883
|
C | T | 1 | a0001c0001t0002g0288 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.390-9966C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359883 | ||||||
| chr4:48359970
|
G | A | 170 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.390-9879G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359970 | ||||||
| chr4:48359971
|
T | C | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-9878T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359971 | ||||||
| chr4:48360151
|
C | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-9698C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360151 | ||||||
| chr4:48360153
|
C | CA | 50 | a0001c0001t0001g0061a0001c0001t0002g0299a0001c0001t0003g0004others(47): Show | 51 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.390-9681dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48360153 | |||||
| chr4:48360153
|
CA | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0121a0001c0001t0002g0244others(4): Show | 7 | HG01255.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.390-9681delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48360153 | |||||
| chr4:48360402
|
C | G | 3 | a0001c0001t0004g0252a0001c0001t0004g0278a0001c0001t0004g0279 | 3 | HG02572.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.390-9447C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360402 | ||||||
| chr4:48360481
|
A | G | 3 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0277 | 3 | NA18957.hp1 NA18970.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.390-9368A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360481 | ||||||
| chr4:48360504
|
A | G | 1 | a0001c0001t0002g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.390-9345A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360504 | ||||||
| chr4:48360524
|
A | G | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(311): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.390-9325A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360524 | ||||||
| chr4:48360534
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.390-9315G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360534 | ||||||
| chr4:48360560
|
C | T | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.390-9289C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360560 | ||||||
| chr4:48360688
|
C | T | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.390-9161C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360688 | ||||||
| chr4:48360839
|
A | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-9010A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360839 | ||||||
| chr4:48360867
|
G | A | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.390-8982G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360867 | ||||||
| chr4:48360892
|
T | C | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.390-8957T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360892 | ||||||
| chr4:48361045
|
G | A | 1 | a0001c0001t0003g0200 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.390-8804G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361045 | ||||||
| chr4:48361199
|
A | T | 3 | a0001c0001t0003g0186a0001c0001t0003g0201a0001c0001t0034g0183 | 3 | NA18963.hp2 NA18992.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.390-8650A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361199 | ||||||
| chr4:48361226
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.390-8623G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361226 | ||||||
| chr4:48361228
|
A | G | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.390-8621A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361228 | ||||||
| chr4:48361352
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.390-8497C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361352 | ||||||
| chr4:48361467
|
G | C | 2 | a0001c0001t0003g0185a0001c0001t0003g0199 | 2 | HG02015.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.390-8382G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361467 | ||||||
| chr4:48361500
|
T | C | 4 | a0001c0001t0003g0182a0001c0001t0003g0202a0001c0001t0003g0206others(1): Show | 4 | HG01516.hp1 NA18943.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-8349T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361500 | ||||||
| chr4:48361624
|
A | AT | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-8215dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48361624 | |||||
| chr4:48361651
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0034others(10): Show | 14 | HG02074.hp2 NA18939.hp1 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-8198C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361651 | ||||||
| chr4:48361657
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.390-8192T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361657 | ||||||
| chr4:48361824
|
GTCT | G | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.390-8020_390-8018d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48361824 | |||||
| chr4:48361966
|
A | G | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.390-7883A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361966 | ||||||
| chr4:48362019
|
G | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-7830G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362019 | ||||||
| chr4:48362232
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-7617C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362232 | ||||||
| chr4:48362358
|
T | C | 1 | a0001c0001t0007g0337 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.390-7491T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362358 | ||||||
| chr4:48362359
|
G | T | 1 | a0001c0001t0007g0337 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.390-7490G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362359 | ||||||
| chr4:48362423
|
C | CT | 31 | a0001c0001t0002g0282a0001c0001t0003g0004a0001c0001t0003g0164others(28): Show | 33 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.390-7412dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362423 | |||||
| chr4:48362423
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.390-7426C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362423 | ||||||
| chr4:48362423
|
CT | C | 12 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0062others(9): Show | 12 | HG00558.hp1 HG01167.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.390-7412delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362423 | |||||
| chr4:48362458
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-7391G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362458 | ||||||
| chr4:48362489
|
G | A | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-7360G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362489 | ||||||
| chr4:48362499
|
ACCTCTGA others(2): Show |
A | 14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 14 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-7346_390-7338d others(11): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362499 | |||||
| chr4:48362566
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.390-7283G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362566 | ||||||
| chr4:48362576
|
G | A | 12 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(9): Show | 13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.390-7273G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362576 | ||||||
| chr4:48362586
|
ATTTTTTT others(30): Show |
A | 25 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(22): Show | 26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.390-7260_390-7224d others(39): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362586 | |||||
| chr4:48362662
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.390-7187G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362662 | ||||||
| chr4:48362732
|
C | CT | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(247): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.390-7103dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362732 | |||||
| chr4:48362732
|
C | CTT | 45 | a0001c0001t0001g0054a0001c0001t0001g0124a0001c0001t0001g0128others(42): Show | 46 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.390-7104_390-7103d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362732 | |||||
| chr4:48362732
|
CTTTTTTT others(12): Show |
C | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(5): Show | 8 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.390-7102_390-7084d others(21): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362732 | |||||
| chr4:48362732
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0001g0156 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.390-7101_390-7082d others(22): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362732 | |||||
| chr4:48362750
|
C | CT | 9 | a0001c0001t0016g0340a0001c0001t0029g0163a0001c0002t0005g0005others(6): Show | 10 | HG01069.hp2 HG01109.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.390-7083dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362750 | |||||
| chr4:48362750
|
CT | C | 119 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0071others(116): Show | 121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.390-7083delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362750 | |||||
| chr4:48362766
|
T | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0002g0255others(1): Show | 4 | HG00642.hp1 HG03486.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-7083T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362766 | ||||||
| chr4:48362767
|
A | T | 21 | a0001c0001t0001g0101a0001c0001t0002g0227a0001c0001t0002g0234others(18): Show | 22 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.390-7082A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362767 | ||||||
| chr4:48362880
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-6969C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362880 | ||||||
| chr4:48362933
|
A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6916A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362933 | ||||||
| chr4:48362934
|
T | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6915T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362934 | ||||||
| chr4:48362951
|
T | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6898T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362951 | ||||||
| chr4:48363006
|
A | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6843A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363006 | ||||||
| chr4:48363044
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-6805C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363044 | ||||||
| chr4:48363061
|
A | G | 1 | a0001c0001t0025g0043 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.390-6788A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363061 | ||||||
| chr4:48363095
|
C | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.390-6754C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363095 | ||||||
| chr4:48363133
|
T | C | 184 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.390-6716T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363133 | ||||||
| chr4:48363277
|
C | T | 2 | a0001c0001t0002g0007a0001c0001t0004g0310 | 3 | HG01074.hp2 HG01099.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.390-6572C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363277 | ||||||
| chr4:48363303
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-6546G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363303 | ||||||
| chr4:48363339
|
C | T | 1 | a0001c0001t0002g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.390-6510C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363339 | ||||||
| chr4:48363372
|
C | T | 1 | a0001c0001t0002g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.390-6477C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363372 | ||||||
| chr4:48363409
|
CCCTCCCG others(42): Show |
C | 1 | a0001c0001t0001g0103 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.390-6414_390-6366d others(51): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363409 | |||||
| chr4:48363419
|
C | T | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-6430C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363419 | ||||||
| chr4:48363433
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.390-6416G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363433 | ||||||
| chr4:48363437
|
GGGGGGCT others(523): Show |
G | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390-6401_390-5872d others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363437 | |||||
| chr4:48363458
|
A | C | 182 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(179): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.390-6391A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363458 | ||||||
| chr4:48363460
|
C | T | 1 | a0001c0002t0005g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.390-6389C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363460 | ||||||
| chr4:48363484
|
A | G | 182 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(179): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.390-6365A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363484 | ||||||
| chr4:48363551
|
C | T | 12 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(9): Show | 13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.390-6298C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363551 | ||||||
| chr4:48363563
|
C | T | 1 | a0001c0001t0002g0315 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.390-6286C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363563 | ||||||
| chr4:48363574
|
ACCCCCCA others(42): Show |
A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6253_390-6205d others(51): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363574 | |||||
| chr4:48363674
|
CACTTCCC others(18): Show |
C | 1 | a0001c0001t0001g0102 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.390-6174_390-6150d others(27): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363674 | ||||||
| chr4:48363674
|
CACTTCCC others(171): Show |
C | 1 | a0001c0001t0017g0241 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.390-6130_390-5953d others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363674 | |||||
| chr4:48363685
|
AGGGGCGG others(467): Show |
A | 1 | a0001c0001t0003g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.390-6146_390-5673d others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363685 | |||||
| chr4:48363691
|
G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6158G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363691 | ||||||
| chr4:48363749
|
AC | A | 153 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(150): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.390-6092delC | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363749 | |||||
| chr4:48363773
|
G | T | 14 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(11): Show | 14 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-6076G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363773 | ||||||
| chr4:48363777
|
C | T | 3 | a0001c0001t0003g0182a0001c0001t0003g0202a0001c0001t0003g0217 | 3 | HG01516.hp1 NA18943.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.390-6072C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363777 | ||||||
| chr4:48363806
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-6043G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363806 | ||||||
| chr4:48363869
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0064 | 2 | HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.390-5980G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363869 | ||||||
| chr4:48363896
|
C | T | 1 | a0001c0002t0031g0178 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.390-5953C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363896 | ||||||
| chr4:48363917
|
C | CG | 41 | a0001c0001t0002g0334a0001c0001t0003g0004a0001c0001t0003g0164others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-5926dupG | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363917 | |||||
| chr4:48363935
|
ACCTC | A | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-5907_390-5904d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363935 | |||||
| chr4:48363946
|
G | A | 156 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(153): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.390-5903G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363946 | ||||||
| chr4:48363955
|
G | T | 40 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(37): Show | 41 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.390-5894G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363955 | ||||||
| chr4:48363967
|
A | G | 192 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.390-5882A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363967 | ||||||
| chr4:48363969
|
G | T | 1 | a0001c0001t0002g0333 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.390-5880G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363969 | ||||||
| chr4:48364011
|
T | C | 193 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.390-5838T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364011 | ||||||
| chr4:48364063
|
C | G | 5 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0041others(2): Show | 5 | HG02074.hp2 NA18965.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.390-5786C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364063 | ||||||
| chr4:48364113
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.390-5736C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364113 | ||||||
| chr4:48364145
|
C | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-5704C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364145 | ||||||
| chr4:48364159
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0029g0163 | 2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.390-5690C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364159 | ||||||
| chr4:48364259
|
C | T | 1 | a0003c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.390-5590C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364259 | ||||||
| chr4:48364280
|
C | T | 3 | a0001c0001t0004g0252a0001c0001t0004g0278a0001c0001t0004g0279 | 3 | HG02572.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.390-5569C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364280 | ||||||
| chr4:48364284
|
G | A | 3 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0101 | 3 | HG00280.hp2 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.390-5565G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364284 | ||||||
| chr4:48364360
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.390-5489C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364360 | ||||||
| chr4:48364429
|
C | T | 158 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(155): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.390-5420C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364429 | ||||||
| chr4:48364430
|
G | A | 10 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-5419G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364430 | ||||||
| chr4:48364437
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.390-5412G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364437 | ||||||
| chr4:48364468
|
C | CG | 6 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0077others(3): Show | 6 | HG01978.hp2 HG02056.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.390-5377dupG | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48364468 | |||||
| chr4:48364468
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-5381C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364468 | ||||||
| chr4:48364500
|
G | A | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.390-5349G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364500 | ||||||
| chr4:48364547
|
C | T | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.390-5302C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364547 | ||||||
| chr4:48364552
|
C | T | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.390-5297C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364552 | ||||||
| chr4:48364639
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.390-5210C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364639 | ||||||
| chr4:48364653
|
C | T | 1 | a0001c0001t0004g0256 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.390-5196C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364653 | ||||||
| chr4:48364677
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-5172C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364677 | ||||||
| chr4:48364682
|
C | G | 2 | a0001c0002t0005g0177a0001c0002t0005g0203 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.390-5167C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364682 | ||||||
| chr4:48364682
|
C | T | 1 | a0001c0001t0002g0284 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.390-5167C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364682 | ||||||
| chr4:48364690
|
A | G | 158 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(155): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.390-5159A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364690 | ||||||
| chr4:48364702
|
T | C | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.390-5147T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364702 | ||||||
| chr4:48364742
|
G | A | 7 | a0001c0001t0002g0227a0001c0001t0002g0234a0001c0001t0002g0235others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.390-5107G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364742 | ||||||
| chr4:48364747
|
C | T | 25 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(22): Show | 26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.390-5102C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364747 | ||||||
| chr4:48364758
|
C | G | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.390-5091C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364758 | ||||||
| chr4:48364851
|
C | T | 2 | a0001c0001t0002g0247a0001c0001t0029g0163 | 2 | HG02258.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.390-4998C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364851 | ||||||
| chr4:48364868
|
G | A | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-4981G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364868 | ||||||
| chr4:48364873
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0003g0182 | 2 | HG01516.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.390-4976A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364873 | ||||||
| chr4:48364873
|
AGGGAGG | A | 19 | a0001c0001t0001g0123a0001c0001t0001g0155a0001c0001t0007g0337others(16): Show | 20 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.390-4956_390-4951d others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48364873 | |||||
| chr4:48364883
|
A | AG | 7 | a0001c0001t0001g0132a0001c0001t0003g0197a0001c0001t0004g0279others(4): Show | 7 | HG01099.hp1 HG02004.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.390-4961dupG | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48364883 | |||||
| chr4:48365044
|
C | T | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.390-4805C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365044 | ||||||
| chr4:48365054
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.390-4795G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365054 | ||||||
| chr4:48365075
|
A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390-4774A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365075 | ||||||
| chr4:48365096
|
C | G | 4 | a0001c0001t0001g0067a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-4753C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365096 | ||||||
| chr4:48365108
|
T | G | 1 | a0001c0001t0001g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.390-4741T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365108 | ||||||
| chr4:48365142
|
G | A | 335 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(332): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.390-4707G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365142 | ||||||
| chr4:48365217
|
C | T | 10 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-4632C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365217 | ||||||
| chr4:48365285
|
A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390-4564A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365285 | ||||||
| chr4:48365300
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-4549C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365300 | ||||||
| chr4:48365331
|
G | A | 11 | a0001c0002t0005g0180a0001c0003t0006g0028a0001c0003t0006g0029others(8): Show | 11 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.390-4518G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365331 | ||||||
| chr4:48365362
|
C | T | 1 | a0001c0001t0024g0010 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.390-4487C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365362 | ||||||
| chr4:48365444
|
C | CA | 105 | a0001c0001t0001g0015a0001c0001t0001g0033a0001c0001t0001g0035others(102): Show | 107 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.390-4384dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365444 | |||||
| chr4:48365444
|
C | CAA | 26 | a0001c0001t0001g0102a0001c0001t0002g0239a0001c0001t0002g0244others(23): Show | 26 | HG00609.hp1 HG01255.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.390-4385_390-4384d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365444 | |||||
| chr4:48365444
|
C | CAAA | 16 | a0001c0001t0023g0031a0001c0002t0005g0005a0001c0002t0005g0173others(13): Show | 17 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.390-4386_390-4384d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365444 | |||||
| chr4:48365444
|
CAA | C | 10 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(7): Show | 10 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.390-4385_390-4384d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365444 | |||||
| chr4:48365468
|
A | G | 1 | a0001c0001t0028g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.390-4381A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365468 | ||||||
| chr4:48365549
|
GTTTA | G | 3 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030 | 3 | HG02258.hp2 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.390-4284_390-4281d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365549 | |||||
| chr4:48365611
|
A | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.390-4238A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365611 | ||||||
| chr4:48365909
|
T | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(144): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.390-3940T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365909 | ||||||
| chr4:48365939
|
TGTAA | T | 25 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(22): Show | 26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.390-3907_390-3904d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365939 | |||||
| chr4:48365951
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.390-3898A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365951 | ||||||
| chr4:48365958
|
A | T | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.390-3891A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365958 | ||||||
| chr4:48366072
|
T | C | 1 | a0001c0001t0003g0200 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.390-3777T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366072 | ||||||
| chr4:48366082
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.390-3767G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366082 | ||||||
| chr4:48366159
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.390-3690C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366159 | ||||||
| chr4:48366402
|
C | T | 2 | a0001c0003t0006g0028a0001c0003t0006g0029 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.390-3447C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366402 | ||||||
| chr4:48366605
|
A | G | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.390-3244A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366605 | ||||||
| chr4:48366690
|
A | G | 1 | a0001c0001t0002g0314 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.390-3159A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366690 | ||||||
| chr4:48366748
|
C | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.390-3101C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366748 | ||||||
| chr4:48366821
|
G | GT | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.390-3021dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48366821 | |||||
| chr4:48366942
|
T | C | 117 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(114): Show | 119 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.390-2907T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366942 | ||||||
| chr4:48367198
|
C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-2651C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367198 | ||||||
| chr4:48367378
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.390-2471A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367378 | ||||||
| chr4:48367693
|
A | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-2156A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367693 | ||||||
| chr4:48367789
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.390-2060A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367789 | ||||||
| chr4:48367801
|
A | G | 1 | a0001c0001t0002g0272 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.390-2048A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367801 | ||||||
| chr4:48367806
|
C | T | 10 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-2043C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367806 | ||||||
| chr4:48367917
|
A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-1932A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367917 | ||||||
| chr4:48367952
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.390-1897C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367952 | ||||||
| chr4:48368051
|
C | CTTTTTTT others(3): Show |
96 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(93): Show | 98 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.390-1794_390-1785d others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | |||||
| chr4:48368051
|
C | CTTTTTTT others(4): Show |
11 | a0001c0001t0002g0288a0001c0001t0002g0289a0001c0001t0002g0298others(8): Show | 11 | HG02074.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.390-1795_390-1785d others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | |||||
| chr4:48368051
|
C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0123others(2): Show | 5 | HG00642.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.390-1796_390-1785d others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | |||||
| chr4:48368051
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0234 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.390-1797_390-1785d others(15): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | |||||
| chr4:48368051
|
C | CTTTTTTT others(7): Show |
12 | a0001c0001t0001g0080a0001c0001t0001g0154a0001c0001t0001g0155others(9): Show | 12 | HG01243.hp2 HG02145.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | |||||
| chr4:48368051
|
C | CTTTTTTT others(8): Show |
17 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(14): Show | 19 | HG01070.hp1 HG01167.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | |||||
| chr4:48368051
|
C | CTTTTTTT others(9): Show |
99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(96): Show | 101 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | |||||
| chr4:48368051
|
C | CTTTTTTT others(10): Show |
42 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0019others(39): Show | 42 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(19): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | |||||
| chr4:48368051
|
C | CTTTTTTT others(11): Show |
10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0068others(7): Show | 10 | HG01257.hp1 HG01361.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(20): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | |||||
| chr4:48368099
|
G | C | 4 | a0001c0001t0008g0142a0001c0001t0008g0144a0001c0001t0008g0145others(1): Show | 4 | HG01256.hp2 HG01496.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-1750G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368099 | ||||||
| chr4:48368419
|
A | AGTACATG others(8): Show |
1 | a0001c0001t0001g0102 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.390-1427_390-1413d others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368419 | |||||
| chr4:48368424
|
A | C | 10 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-1425A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368424 | ||||||
| chr4:48368480
|
ATT | A | 10 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(7): Show | 10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-1368_390-1367d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368480 | ||||||
| chr4:48368495
|
A | G | 1 | a0001c0001t0004g0258 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.390-1354A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368495 | ||||||
| chr4:48368525
|
A | T | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390-1324A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368525 | ||||||
| chr4:48368595
|
AC | A | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.390-1253delC | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368595 | ||||||
| chr4:48368608
|
T | G | 1 | a0001c0001t0001g0081 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.390-1241T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368608 | ||||||
| chr4:48368799
|
G | C | 1 | a0001c0001t0007g0337 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.390-1050G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368799 | ||||||
| chr4:48369381
|
C | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.390-468C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48369381 | ||||||
| chr4:48369501
|
T | C | 116 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(113): Show | 118 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.390-348T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48369501 | ||||||
| chr4:48369741
|
A | G | 1 | a0001c0001t0002g0306 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.390-108A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48369741 | ||||||
| chr4:48369751
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.390-98C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48369751 | ||||||
| chr4:48370001
|
T | A | 1 | a0001c0001t0001g0102 | 1 | NA19078.hp1 | splice_region_variant&intron_variant | LOW | c.538+4T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370001 | ||||||
| chr4:48370046
|
C | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0082 | 2 | HG00558.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.538+49C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370046 | ||||||
| chr4:48370068
|
T | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.538+71T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370068 | ||||||
| chr4:48370202
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.538+205A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370202 | ||||||
| chr4:48370389
|
G | C | 15 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(12): Show | 16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.538+392G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370389 | ||||||
| chr4:48370537
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.538+540A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370537 | ||||||
| chr4:48370718
|
C | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.538+721C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370718 | ||||||
| chr4:48371102
|
T | C | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.538+1105T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371102 | ||||||
| chr4:48371109
|
G | GT | 21 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0001g0068others(18): Show | 21 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.538+1126dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371109 | |||||
| chr4:48371109
|
GT | G | 25 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(22): Show | 26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.538+1126delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371109 | |||||
| chr4:48371114
|
T | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0108 | 2 | NA19010.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.538+1117T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371114 | ||||||
| chr4:48371253
|
T | G | 1 | a0001c0001t0001g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.538+1256T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371253 | ||||||
| chr4:48371270
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.538+1273A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371270 | ||||||
| chr4:48371510
|
A | T | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.538+1513A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371510 | ||||||
| chr4:48371663
|
A | C | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1666A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371663 | ||||||
| chr4:48371665
|
T | A | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1668T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371665 | ||||||
| chr4:48371666
|
C | T | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1669C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371666 | ||||||
| chr4:48371667
|
C | A | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1670C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371667 | ||||||
| chr4:48371668
|
T | C | 4 | a0001c0001t0002g0246a0001c0001t0003g0182a0001c0001t0003g0202others(1): Show | 4 | HG01516.hp1 NA18940.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+1671T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371668 | ||||||
| chr4:48371670
|
G | T | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1673G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371670 | ||||||
| chr4:48371673
|
G | T | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1676G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371673 | ||||||
| chr4:48371675
|
C | A | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1678C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371675 | ||||||
| chr4:48371677
|
A | G | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1680A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371677 | ||||||
| chr4:48371678
|
G | T | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1681G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371678 | ||||||
| chr4:48371679
|
G | T | 1 | a0001c0001t0002g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1682G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371679 | ||||||
| chr4:48371771
|
A | G | 15 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(12): Show | 16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.538+1774A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371771 | ||||||
| chr4:48371926
|
G | A | 1 | a0001c0001t0002g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.538+1929G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371926 | ||||||
| chr4:48371940
|
CCAAAA | C | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.538+1958_538+1962d others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371940 | |||||
| chr4:48371971
|
T | TAC | 3 | a0001c0001t0003g0207a0001c0001t0003g0208a0001c0001t0003g0209 | 3 | HG00099.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.538+1991_538+1992d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371971 | |||||
| chr4:48371971
|
TAC | T | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(234): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.538+1991_538+1992d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371971 | |||||
| chr4:48371971
|
TACAC | T | 24 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(21): Show | 26 | HG01255.hp1 HG01891.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.538+1989_538+1992d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371971 | |||||
| chr4:48371971
|
TACACAC | T | 17 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(14): Show | 18 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.538+1987_538+1992d others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371971 | |||||
| chr4:48371972
|
ACACACAC others(15): Show |
A | 4 | a0001c0001t0002g0243a0001c0001t0002g0308a0001c0001t0002g0311others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+1993_538+2014d others(24): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371972 | |||||
| chr4:48371986
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.538+1989A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371986 | ||||||
| chr4:48371988
|
A | G | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(159): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.538+1991A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371988 | ||||||
| chr4:48371994
|
G | A | 5 | a0001c0001t0001g0049a0001c0001t0002g0253a0001c0001t0002g0316others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.538+1997G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371994 | ||||||
| chr4:48371996
|
A | G | 29 | a0001c0001t0001g0039a0001c0001t0001g0121a0001c0001t0002g0289others(26): Show | 30 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.538+1999A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371996 | ||||||
| chr4:48371998
|
A | G | 3 | a0001c0002t0030g0205a0001c0003t0006g0028a0001c0003t0006g0029 | 3 | HG02258.hp2 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.538+2001A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371998 | ||||||
| chr4:48372029
|
TATATATA others(7): Show |
T | 1 | a0001c0003t0006g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.538+2046_538+2059d others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48372029 | |||||
| chr4:48372031
|
TATATAC | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+2046_538+2051d others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48372031 | |||||
| chr4:48372037
|
CATATACA others(9): Show |
C | 9 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(6): Show | 9 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+2046_538+2061d others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48372037 | |||||
| chr4:48372039
|
T | C | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.538+2042T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372039 | ||||||
| chr4:48372051
|
CAT | C | 128 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(125): Show | 131 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.538+2066_538+2067d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48372051 | |||||
| chr4:48372063
|
T | C | 1 | a0001c0003t0006g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.538+2066T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372063 | ||||||
| chr4:48372125
|
T | A | 1 | a0001c0003t0006g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.538+2128T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372125 | ||||||
| chr4:48372187
|
T | C | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.538+2190T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372187 | ||||||
| chr4:48372201
|
A | C | 1 | a0001c0001t0001g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.538+2204A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372201 | ||||||
| chr4:48372315
|
T | C | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+2318T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372315 | ||||||
| chr4:48372351
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0226 | 3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.538+2354T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372351 | ||||||
| chr4:48372388
|
A | G | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.538+2391A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372388 | ||||||
| chr4:48372400
|
T | A | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.538+2403T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372400 | ||||||
| chr4:48372500
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.538+2503A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372500 | ||||||
| chr4:48372505
|
A | G | 2 | a0001c0003t0012g0221a0001c0003t0012g0222 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.538+2508A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372505 | ||||||
| chr4:48372532
|
G | A | 11 | a0001c0001t0029g0163a0001c0003t0006g0028a0001c0003t0006g0029others(8): Show | 11 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.538+2535G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372532 | ||||||
| chr4:48372572
|
A | C | 1 | a0001c0001t0001g0047 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.538+2575A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372572 | ||||||
| chr4:48372635
|
C | T | 125 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(122): Show | 127 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.538+2638C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372635 | ||||||
| chr4:48372888
|
T | G | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.538+2891T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372888 | ||||||
| chr4:48372986
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.538+2989C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372986 | ||||||
| chr4:48372997
|
A | G | 1 | a0001c0001t0013g0293 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.538+3000A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372997 | ||||||
| chr4:48373257
|
C | T | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.538+3260C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373257 | ||||||
| chr4:48373568
|
G | A | 3 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0212 | 3 | HG00735.hp1 HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.538+3571G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373568 | ||||||
| chr4:48373573
|
G | C | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.538+3576G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373573 | ||||||
| chr4:48373762
|
C | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+3765C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373762 | ||||||
| chr4:48373773
|
GCTTACAC others(14): Show |
G | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.538+3780_538+3800d others(23): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48373773 | |||||
| chr4:48373838
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.538+3841C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373838 | ||||||
| chr4:48373843
|
C | A | 1 | a0001c0001t0034g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.538+3846C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373843 | ||||||
| chr4:48373920
|
C | T | 9 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+3923C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373920 | ||||||
| chr4:48373993
|
G | A | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-3903G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373993 | ||||||
| chr4:48374081
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-3815G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374081 | ||||||
| chr4:48374093
|
G | C | 1 | a0001c0001t0002g0230 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.539-3803G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374093 | ||||||
| chr4:48374179
|
A | G | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-3717A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374179 | ||||||
| chr4:48374260
|
G | A | 1 | a0001c0001t0002g0284 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.539-3636G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374260 | ||||||
| chr4:48374339
|
C | T | 1 | a0001c0001t0003g0164 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.539-3557C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374339 | ||||||
| chr4:48374396
|
C | G | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.539-3500C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374396 | ||||||
| chr4:48374586
|
G | A | 2 | a0001c0001t0002g0234a0001c0001t0002g0315 | 2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.539-3310G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374586 | ||||||
| chr4:48374762
|
A | T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-3134A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374762 | ||||||
| chr4:48374782
|
G | T | 1 | a0001c0001t0002g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.539-3114G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374782 | ||||||
| chr4:48374785
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.539-3111A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374785 | ||||||
| chr4:48374789
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(117): Show | 122 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.539-3107A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374789 | ||||||
| chr4:48374802
|
A | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.539-3094A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374802 | ||||||
| chr4:48374834
|
T | A | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.539-3062T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374834 | ||||||
| chr4:48375036
|
T | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.539-2860T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375036 | ||||||
| chr4:48375109
|
G | A | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-2787G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375109 | ||||||
| chr4:48375119
|
G | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.539-2777G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375119 | ||||||
| chr4:48375120
|
A | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.539-2776A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375120 | ||||||
| chr4:48375223
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.539-2673G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375223 | ||||||
| chr4:48375271
|
C | T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-2625C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375271 | ||||||
| chr4:48375302
|
T | A | 2 | a0001c0003t0006g0028a0001c0003t0006g0029 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.539-2594T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375302 | ||||||
| chr4:48375390
|
C | T | 1 | a0001c0001t0004g0295 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.539-2506C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375390 | ||||||
| chr4:48375495
|
C | CT | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG02109.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-2393dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48375495 | |||||
| chr4:48375616
|
A | G | 3 | a0001c0004t0002g0236a0001c0004t0002g0237a0001c0004t0002g0238 | 3 | HG02451.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.539-2280A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375616 | ||||||
| chr4:48375670
|
G | A | 1 | a0003c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.539-2226G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375670 | ||||||
| chr4:48375845
|
A | G | 15 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(12): Show | 16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-2051A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375845 | ||||||
| chr4:48375911
|
C | T | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-1985C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375911 | ||||||
| chr4:48376144
|
G | T | 1 | a0001c0002t0005g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.539-1752G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376144 | ||||||
| chr4:48376228
|
C | T | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-1668C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376228 | ||||||
| chr4:48376246
|
G | A | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.539-1650G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376246 | ||||||
| chr4:48376251
|
C | T | 1 | a0001c0001t0002g0271 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.539-1645C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376251 | ||||||
| chr4:48376369
|
C | A | 25 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(22): Show | 26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.539-1527C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376369 | ||||||
| chr4:48376411
|
C | T | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-1485C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376411 | ||||||
| chr4:48376456
|
GAA | G | 125 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(122): Show | 127 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.539-1423_539-1422d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376456 | |||||
| chr4:48376456
|
GAAA | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.539-1424_539-1422d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376456 | |||||
| chr4:48376475
|
G | C | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.539-1421G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376475 | ||||||
| chr4:48376562
|
A | C | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.539-1334A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376562 | ||||||
| chr4:48376619
|
C | CT | 19 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0033others(16): Show | 19 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.539-1257dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376619 | |||||
| chr4:48376619
|
CT | C | 20 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0026others(17): Show | 20 | HG00741.hp2 HG01255.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.539-1257delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376619 | |||||
| chr4:48376619
|
CTT | C | 139 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(136): Show | 142 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.539-1258_539-1257d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376619 | |||||
| chr4:48376639
|
T | G | 2 | a0001c0001t0011g0017a0001c0001t0011g0027 | 2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.539-1257T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376639 | ||||||
| chr4:48376744
|
C | T | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.539-1152C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376744 | ||||||
| chr4:48376771
|
C | G | 1 | a0001c0001t0004g0270 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.539-1125C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376771 | ||||||
| chr4:48376824
|
C | T | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-1072C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376824 | ||||||
| chr4:48376833
|
G | A | 1 | a0001c0003t0006g0220 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539-1063G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376833 | ||||||
| chr4:48376853
|
C | T | 1 | a0001c0001t0004g0269 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.539-1043C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376853 | ||||||
| chr4:48376902
|
C | T | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.539-994C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376902 | ||||||
| chr4:48376913
|
C | CT | 32 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0035others(29): Show | 34 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.539-962dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376913 | |||||
| chr4:48376913
|
CT | C | 178 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0044others(175): Show | 180 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.539-962delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376913 | |||||
| chr4:48376965
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-931G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376965 | ||||||
| chr4:48376989
|
TA | T | 25 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(22): Show | 26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.539-897delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376989 | |||||
| chr4:48376999
|
A | T | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-897A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376999 | ||||||
| chr4:48377102
|
A | T | 1 | a0001c0001t0003g0201 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.539-794A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377102 | ||||||
| chr4:48377185
|
T | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.539-711T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377185 | ||||||
| chr4:48377194
|
A | T | 1 | a0001c0001t0010g0089 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.539-702A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377194 | ||||||
| chr4:48377207
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.539-689G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377207 | ||||||
| chr4:48377316
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.539-580T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377316 | ||||||
| chr4:48377336
|
A | AT | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.539-539dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48377336 | |||||
| chr4:48377336
|
AT | A | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(3): Show | 6 | HG01167.hp1 HG01256.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.539-539delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48377336 | |||||
| chr4:48377398
|
C | T | 1 | a0003c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.539-498C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377398 | ||||||
| chr4:48377447
|
G | A | 14 | a0001c0001t0027g0181a0001c0002t0005g0005a0001c0002t0005g0173others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-449G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377447 | ||||||
| chr4:48377849
|
C | G | 3 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030 | 3 | HG02258.hp2 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.539-47C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377849 | ||||||
| chr4:48378078
|
T | C | 1 | a0001c0003t0006g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.703+18T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378078 | ||||||
| chr4:48378191
|
G | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.703+131G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378191 | ||||||
| chr4:48378229
|
C | T | 3 | a0001c0001t0003g0186a0001c0001t0003g0201a0001c0001t0034g0183 | 3 | NA18963.hp2 NA18992.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.703+169C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378229 | ||||||
| chr4:48378342
|
T | G | 13 | a0001c0001t0029g0163a0001c0002t0030g0205a0001c0003t0006g0028others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.703+282T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378342 | ||||||
| chr4:48378463
|
A | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(157): Show | 165 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.703+403A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378463 | ||||||
| chr4:48378531
|
A | G | 3 | a0001c0001t0003g0207a0001c0001t0003g0208a0001c0001t0003g0209 | 3 | HG00099.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.703+471A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378531 | ||||||
| chr4:48378580
|
C | T | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703+520C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378580 | ||||||
| chr4:48378582
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.703+522A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378582 | ||||||
| chr4:48378775
|
G | C | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.703+715G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378775 | ||||||
| chr4:48378847
|
T | C | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+787T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378847 | ||||||
| chr4:48379048
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.704-642C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48379048 | ||||||
| chr4:48379265
|
T | C | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.704-425T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48379265 | ||||||
| chr4:48379305
|
C | T | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.704-385C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48379305 | ||||||
| chr4:48379558
|
A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704-132A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48379558 | ||||||
| chr4:48379673
|
CT | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0156others(6): Show | 9 | HG01256.hp2 HG02615.hp1 HG02809.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.704-4delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 48379673 | |||||
| chr4:48379893
|
T | C | 13 | a0001c0001t0029g0163a0001c0002t0030g0205a0001c0003t0006g0028others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.862+45T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48379893 | ||||||
| chr4:48379942
|
T | C | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.862+94T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48379942 | ||||||
| chr4:48380000
|
A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.862+152A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380000 | ||||||
| chr4:48380066
|
A | G | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.862+218A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380066 | ||||||
| chr4:48380096
|
A | G | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.862+248A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380096 | ||||||
| chr4:48380526
|
C | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(294): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.862+678C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380526 | ||||||
| chr4:48380775
|
C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.862+927C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380775 | ||||||
| chr4:48381075
|
G | A | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.862+1227G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381075 | ||||||
| chr4:48381475
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.863-1093A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381475 | ||||||
| chr4:48381548
|
C | T | 1 | a0001c0001t0002g0281 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.863-1020C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381548 | ||||||
| chr4:48381655
|
C | A | 1 | a0001c0001t0003g0217 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.863-913C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381655 | ||||||
| chr4:48381753
|
G | A | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.863-815G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381753 | ||||||
| chr4:48382482
|
T | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.863-86T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48382482 | ||||||
| chr4:48382974
|
G | A | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1222+47G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48382974 | ||||||
| chr4:48383038
|
C | T | 1 | a0001c0001t0002g0235 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1222+111C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383038 | ||||||
| chr4:48383080
|
A | C | 1 | a0001c0001t0002g0306 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1222+153A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383080 | ||||||
| chr4:48383102
|
A | C | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1222+175A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383102 | ||||||
| chr4:48383167
|
TC | T | 7 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(4): Show | 7 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+241delC | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383167 | ||||||
| chr4:48383168
|
C | CA | 7 | a0001c0001t0002g0333a0001c0001t0004g0259a0001c0001t0004g0295others(4): Show | 7 | HG03139.hp2 HG03225.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+262dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 48383168 | |||||
| chr4:48383168
|
CA | C | 18 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0079others(15): Show | 18 | HG01070.hp2 HG01257.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.1222+262delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 48383168 | |||||
| chr4:48383168
|
CAA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1222+261_1222+262d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 48383168 | |||||
| chr4:48383168
|
CAAA | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0036others(14): Show | 17 | HG00733.hp2 HG00738.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1222+260_1222+262d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 48383168 | |||||
| chr4:48383185
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0093others(1): Show | 4 | NA18943.hp1 NA19012.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222+258A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383185 | ||||||
| chr4:48383194
|
C | A | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1222+267C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383194 | ||||||
| chr4:48383240
|
A | C | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+313A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383240 | ||||||
| chr4:48383487
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1223-160C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383487 | ||||||
| chr4:48383604
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1223-43T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383604 | ||||||
| chr4:48383958
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1360+174A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48383958 | ||||||
| chr4:48384056
|
A | G | 1 | a0001c0003t0006g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1360+272A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384056 | ||||||
| chr4:48384076
|
TTTTGCTT others(17): Show |
T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+293_1360+316d others(26): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384076 | ||||||
| chr4:48384145
|
C | T | 1 | a0001c0001t0007g0330 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1360+361C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384145 | ||||||
| chr4:48384158
|
T | C | 1 | a0001c0001t0003g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1360+374T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384158 | ||||||
| chr4:48384206
|
T | G | 1 | a0001c0001t0002g0297 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1360+422T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384206 | ||||||
| chr4:48384251
|
A | G | 1 | a0001c0001t0003g0186 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1360+467A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384251 | ||||||
| chr4:48384312
|
C | T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+528C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384312 | ||||||
| chr4:48384335
|
A | G | 1 | a0001c0001t0004g0232 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1360+551A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384335 | ||||||
| chr4:48384581
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1360+797A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384581 | ||||||
| chr4:48384800
|
C | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1360+1016C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384800 | ||||||
| chr4:48384874
|
C | T | 2 | a0001c0001t0002g0289a0001c0001t0007g0337 | 2 | HG02602.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1360+1090C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384874 | ||||||
| chr4:48384905
|
T | G | 1 | a0001c0001t0004g0260 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1360+1121T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384905 | ||||||
| chr4:48384914
|
A | G | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+1130A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384914 | ||||||
| chr4:48385056
|
T | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1360+1272T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385056 | ||||||
| chr4:48385505
|
T | C | 1 | a0001c0001t0002g0244 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1360+1721T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385505 | ||||||
| chr4:48385638
|
C | CT | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1360+1864dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48385638 | |||||
| chr4:48385748
|
G | A | 1 | a0001c0001t0034g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1360+1964G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385748 | ||||||
| chr4:48385811
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1360+2027T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385811 | ||||||
| chr4:48385834
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(35): Show | 40 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1360+2050T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385834 | ||||||
| chr4:48385942
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1360+2158G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385942 | ||||||
| chr4:48385942
|
G | GT | 6 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0082others(3): Show | 7 | HG00558.hp1 HG02155.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1360+2171dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48385942 | |||||
| chr4:48386090
|
GA | G | 11 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0073others(8): Show | 11 | HG00408.hp1 HG02056.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+2325delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48386090 | |||||
| chr4:48386090
|
GAA | G | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+2324_1360+232 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48386090 | |||||
| chr4:48386100
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1360+2316A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386100 | ||||||
| chr4:48386107
|
A | C | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1360+2323A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386107 | ||||||
| chr4:48386275
|
C | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1360+2491C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386275 | ||||||
| chr4:48386286
|
A | G | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+2502A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386286 | ||||||
| chr4:48386357
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1360+2573G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386357 | ||||||
| chr4:48386489
|
A | G | 1 | a0001c0001t0002g0268 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1360+2705A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386489 | ||||||
| chr4:48386594
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0116 | 2 | NA18946.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1360+2810A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386594 | ||||||
| chr4:48386640
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1360+2856C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386640 | ||||||
| chr4:48386752
|
G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0109 | 2 | HG00558.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1360+2968G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386752 | ||||||
| chr4:48386758
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1360+2974T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386758 | ||||||
| chr4:48386806
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+3022C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386806 | ||||||
| chr4:48386844
|
G | A | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+3060G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386844 | ||||||
| chr4:48386865
|
A | G | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+3081A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386865 | ||||||
| chr4:48386962
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1360+3178C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386962 | ||||||
| chr4:48387094
|
C | G | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+3310C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387094 | ||||||
| chr4:48387124
|
C | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+3340C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387124 | ||||||
| chr4:48387133
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1360+3349T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387133 | ||||||
| chr4:48387208
|
A | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+3424A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387208 | ||||||
| chr4:48387220
|
T | A | 2 | a0001c0001t0002g0302a0001c0001t0002g0314 | 2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1360+3436T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387220 | ||||||
| chr4:48387244
|
A | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0226 | 3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1360+3460A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387244 | ||||||
| chr4:48387416
|
A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+3632A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387416 | ||||||
| chr4:48387486
|
A | G | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+3702A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387486 | ||||||
| chr4:48387577
|
G | C | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+3793G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387577 | ||||||
| chr4:48387643
|
C | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+3859C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387643 | ||||||
| chr4:48387692
|
A | G | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1360+3908A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387692 | ||||||
| chr4:48387764
|
A | G | 1 | a0001c0001t0002g0243 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1360+3980A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387764 | ||||||
| chr4:48387801
|
AATAT | A | 4 | a0001c0001t0002g0304a0001c0001t0002g0333a0001c0001t0015g0303others(1): Show | 4 | HG02717.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1360+4022_1360+402 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48387801 | |||||
| chr4:48388560
|
T | C | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+4776T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48388560 | ||||||
| chr4:48388608
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1360+4824A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48388608 | ||||||
| chr4:48388812
|
C | T | 1 | a0001c0001t0002g0333 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1360+5028C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48388812 | ||||||
| chr4:48389109
|
TAA | T | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+5326_1360+532 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389109 | ||||||
| chr4:48389200
|
A | G | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+5416A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389200 | ||||||
| chr4:48389362
|
C | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1360+5578C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389362 | ||||||
| chr4:48389392
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1360+5608A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389392 | ||||||
| chr4:48389471
|
A | G | 1 | a0001c0001t0002g0230 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1360+5687A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389471 | ||||||
| chr4:48389483
|
T | C | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+5699T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389483 | ||||||
| chr4:48389511
|
C | T | 1 | a0001c0001t0004g0270 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1360+5727C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389511 | ||||||
| chr4:48389667
|
G | A | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0226 | 3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1360+5883G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389667 | ||||||
| chr4:48389764
|
A | T | 1 | a0001c0004t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1360+5980A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389764 | ||||||
| chr4:48389811
|
A | G | 1 | a0001c0001t0003g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1360+6027A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389811 | ||||||
| chr4:48389927
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1360+6143T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389927 | ||||||
| chr4:48389945
|
A | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(179): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.1360+6161A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389945 | ||||||
| chr4:48390078
|
CTTTTTCT others(6): Show |
C | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1360+6300_1360+631 others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48390078 | |||||
| chr4:48390084
|
C | CT | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(140): Show | 147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1360+6314dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48390084 | |||||
| chr4:48390191
|
C | T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+6407C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390191 | ||||||
| chr4:48390226
|
C | T | 1 | a0001c0001t0002g0266 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1360+6442C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390226 | ||||||
| chr4:48390245
|
T | C | 2 | a0001c0003t0012g0221a0001c0003t0012g0222 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1360+6461T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390245 | ||||||
| chr4:48390266
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1360+6482A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390266 | ||||||
| chr4:48390622
|
A | G | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1360+6838A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390622 | ||||||
| chr4:48390641
|
T | G | 1 | a0001c0003t0006g0223 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1360+6857T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390641 | ||||||
| chr4:48390741
|
G | A | 1 | a0001c0001t0013g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1360+6957G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390741 | ||||||
| chr4:48390924
|
A | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(22): Show | 27 | HG00642.hp1 HG01255.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+7140A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390924 | ||||||
| chr4:48391193
|
G | A | 1 | a0001c0001t0002g0316 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1360+7409G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391193 | ||||||
| chr4:48391417
|
G | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1360+7633G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391417 | ||||||
| chr4:48391542
|
T | A | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+7758T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391542 | ||||||
| chr4:48391663
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1360+7879A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391663 | ||||||
| chr4:48391704
|
A | G | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+7920A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391704 | ||||||
| chr4:48391977
|
C | G | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+8193C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391977 | ||||||
| chr4:48392062
|
CAG | C | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+8281_1360+828 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48392062 | |||||
| chr4:48392101
|
G | A | 1 | a0001c0002t0005g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1360+8317G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392101 | ||||||
| chr4:48392307
|
G | A | 2 | a0001c0001t0003g0182a0001c0001t0003g0202 | 2 | HG01516.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1360+8523G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392307 | ||||||
| chr4:48392337
|
T | A | 20 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(17): Show | 22 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1360+8553T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392337 | ||||||
| chr4:48392397
|
A | G | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+8613A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392397 | ||||||
| chr4:48392433
|
T | C | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1360+8649T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392433 | ||||||
| chr4:48392557
|
G | A | 2 | a0001c0003t0012g0221a0001c0003t0012g0222 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1360+8773G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392557 | ||||||
| chr4:48392576
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1360+8792T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392576 | ||||||
| chr4:48392576
|
T | G | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+8792T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392576 | ||||||
| chr4:48392598
|
A | G | 1 | a0001c0001t0002g0329 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1360+8814A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392598 | ||||||
| chr4:48392796
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1360+9012C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392796 | ||||||
| chr4:48392798
|
A | G | 116 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(113): Show | 118 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1360+9014A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392798 | ||||||
| chr4:48392858
|
T | G | 2 | a0001c0001t0004g0324a0001c0001t0004g0325 | 2 | NA18950.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1360+9074T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392858 | ||||||
| chr4:48392900
|
A | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+9116A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392900 | ||||||
| chr4:48392980
|
G | A | 13 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0067others(10): Show | 13 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1360+9196G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392980 | ||||||
| chr4:48392996
|
A | G | 1 | a0001c0001t0026g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1360+9212A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392996 | ||||||
| chr4:48392999
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1360+9215A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392999 | ||||||
| chr4:48393312
|
C | T | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+9528C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393312 | ||||||
| chr4:48393386
|
T | TTG | 8 | a0001c0001t0001g0082a0001c0001t0001g0224a0001c0001t0003g0187others(5): Show | 8 | HG02155.hp1 HG02886.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360+9638_1360+963 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
T | TTGTG | 9 | a0001c0001t0001g0059a0001c0001t0001g0101a0001c0001t0001g0103others(6): Show | 9 | HG01515.hp2 HG02015.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+9636_1360+963 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
T | TTGTGTG | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(70): Show | 75 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1360+9634_1360+963 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
T | TTGTGTGT others(1): Show |
162 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(159): Show | 167 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1360+9632_1360+963 others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
T | TTGTGTGT others(3): Show |
17 | a0001c0001t0001g0016a0001c0001t0001g0049a0001c0001t0001g0067others(14): Show | 17 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1360+9630_1360+963 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
T | TTGTGTGT others(5): Show |
7 | a0001c0001t0002g0265a0001c0001t0002g0300a0001c0001t0002g0302others(4): Show | 7 | HG00099.hp2 HG02523.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1360+9628_1360+963 others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
T | TTGTGTGT others(7): Show |
5 | a0001c0001t0001g0050a0001c0001t0001g0109a0001c0001t0002g0229others(2): Show | 5 | HG00558.hp2 HG01255.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+9626_1360+963 others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
T | TTGTGTGT others(9): Show |
6 | a0001c0001t0002g0332a0001c0002t0009g0171a0001c0002t0009g0172others(3): Show | 6 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1360+9624_1360+963 others(20): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
T | TTTGTGTG others(6): Show |
1 | a0001c0003t0012g0222 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1360+9603_1360+960 others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
T | TTTGTGTG others(12): Show |
1 | a0001c0003t0012g0221 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1360+9603_1360+960 others(23): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393386
|
TTG | T | 5 | a0001c0001t0001g0158a0001c0001t0003g0182a0001c0001t0003g0202others(2): Show | 5 | HG00099.hp1 HG01433.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+9638_1360+963 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | |||||
| chr4:48393387
|
TGTGTGTG others(8): Show |
T | 9 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1360+9604_1360+961 others(19): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393387 | ||||||
| chr4:48393439
|
G | C | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+9655G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393439 | ||||||
| chr4:48393735
|
C | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+9951C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393735 | ||||||
| chr4:48393781
|
A | G | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+9997A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393781 | ||||||
| chr4:48393801
|
A | G | 1 | a0001c0002t0005g0180 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1360+10017A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393801 | ||||||
| chr4:48393972
|
A | G | 3 | a0001c0001t0002g0243a0001c0001t0002g0308a0001c0001t0002g0311 | 3 | HG01070.hp2 HG01071.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1360+10188A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393972 | ||||||
| chr4:48393991
|
G | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1360+10207G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393991 | ||||||
| chr4:48393993
|
A | G | 27 | a0001c0001t0016g0340a0001c0001t0029g0163a0001c0002t0005g0005others(24): Show | 28 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1360+10209A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393993 | ||||||
| chr4:48394150
|
C | T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+10366C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394150 | ||||||
| chr4:48394319
|
A | G | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+10535A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394319 | ||||||
| chr4:48394479
|
C | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(295): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1360+10695C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394479 | ||||||
| chr4:48394736
|
G | T | 3 | a0001c0001t0002g0253a0001c0001t0002g0316a0001c0001t0002g0317 | 3 | HG02055.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1360+10952G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394736 | ||||||
| chr4:48394767
|
A | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+10983A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394767 | ||||||
| chr4:48394924
|
T | A | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+11140T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394924 | ||||||
| chr4:48395014
|
A | G | 1 | a0001c0001t0002g0277 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1360+11230A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395014 | ||||||
| chr4:48395031
|
C | T | 1 | a0001c0002t0005g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1360+11247C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395031 | ||||||
| chr4:48395043
|
G | T | 1 | a0001c0001t0007g0330 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1360+11259G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395043 | ||||||
| chr4:48395139
|
A | T | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1360+11355A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395139 | ||||||
| chr4:48395260
|
C | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0067others(8): Show | 11 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1360+11476C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395260 | ||||||
| chr4:48395445
|
G | T | 2 | a0001c0001t0002g0302a0001c0001t0002g0314 | 2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1360+11661G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395445 | ||||||
| chr4:48395445
|
GA | G | 107 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(104): Show | 109 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1360+11671delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395445 | |||||
| chr4:48395446
|
A | G | 2 | a0001c0001t0002g0302a0001c0001t0002g0314 | 2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1360+11662A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395446 | ||||||
| chr4:48395458
|
A | G | 1 | a0001c0001t0002g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1360+11674A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395458 | ||||||
| chr4:48395477
|
C | T | 38 | a0001c0001t0002g0228a0001c0001t0002g0239a0001c0001t0002g0240others(35): Show | 38 | HG00597.hp2 HG01346.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.1360+11693C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395477 | ||||||
| chr4:48395607
|
G | A | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+11823G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395607 | ||||||
| chr4:48395675
|
A | G | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+11891A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395675 | ||||||
| chr4:48395729
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0071 | 2 | NA18941.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1360+11945T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395729 | ||||||
| chr4:48395780
|
G | T | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+11996G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395780 | ||||||
| chr4:48395810
|
C | CTTT | 6 | a0001c0003t0006g0032a0001c0003t0006g0218a0001c0003t0006g0219others(3): Show | 6 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1360+12042_1360+12 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
C | CTTTT | 9 | a0001c0001t0001g0009a0001c0001t0001g0046a0001c0001t0001g0061others(6): Show | 9 | HG01070.hp1 HG01175.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+12041_1360+12 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
C | CTTTTT | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1360+12040_1360+12 others(11): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
C | CTTTTTT | 102 | a0001c0001t0001g0085a0001c0001t0001g0093a0001c0001t0001g0143others(99): Show | 104 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1360+12039_1360+12 others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
C | CTTTTTTT | 15 | a0001c0001t0001g0094a0001c0001t0002g0246a0001c0001t0002g0247others(12): Show | 15 | HG00741.hp1 HG02004.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+12038_1360+12 others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0003g0182a0001c0001t0003g0202a0001c0001t0003g0217others(4): Show | 7 | HG01516.hp1 HG02630.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1360+12036_1360+12 others(15): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(8): Show | 11 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1360+12035_1360+12 others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+12031_1360+12 others(20): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
C | CTTTTTTT others(14): Show |
1 | a0001c0003t0012g0222 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1360+12044_1360+12 others(27): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
C | CTTTTTTT others(15): Show |
1 | a0001c0003t0012g0221 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1360+12044_1360+12 others(28): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395810
|
CTTTTT | C | 11 | a0001c0002t0005g0005a0001c0002t0005g0174a0001c0002t0005g0175others(8): Show | 12 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1360+12040_1360+12 others(11): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | |||||
| chr4:48395901
|
A | G | 1 | a0001c0006t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1360+12117A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395901 | ||||||
| chr4:48395909
|
A | G | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1360+12125A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395909 | ||||||
| chr4:48395982
|
G | T | 1 | a0001c0001t0002g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1360+12198G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395982 | ||||||
| chr4:48396219
|
A | C | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+12435A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396219 | ||||||
| chr4:48396331
|
A | C | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(316): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1360+12547A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396331 | ||||||
| chr4:48396334
|
G | A | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1360+12550G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396334 | ||||||
| chr4:48396405
|
A | C | 1 | a0001c0001t0026g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1360+12621A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396405 | ||||||
| chr4:48396466
|
A | G | 1 | a0001c0001t0025g0043 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1360+12682A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396466 | ||||||
| chr4:48396660
|
C | A | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+12876C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396660 | ||||||
| chr4:48396718
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+12934C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396718 | ||||||
| chr4:48396760
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+12976G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396760 | ||||||
| chr4:48396798
|
C | T | 1 | a0001c0001t0002g0287 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1360+13014C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396798 | ||||||
| chr4:48396958
|
G | A | 3 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030 | 3 | HG02258.hp2 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1360+13174G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396958 | ||||||
| chr4:48397283
|
T | C | 1 | a0001c0001t0002g0282 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1360+13499T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397283 | ||||||
| chr4:48397362
|
T | C | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+13578T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397362 | ||||||
| chr4:48397404
|
T | C | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+13620T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397404 | ||||||
| chr4:48397471
|
T | C | 4 | a0001c0003t0006g0218a0001c0003t0006g0219a0001c0003t0006g0220others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360+13687T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397471 | ||||||
| chr4:48397498
|
T | G | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+13714T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397498 | ||||||
| chr4:48397627
|
A | G | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+13843A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397627 | ||||||
| chr4:48397664
|
C | T | 1 | a0001c0001t0003g0216 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1360+13880C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397664 | ||||||
| chr4:48397861
|
C | T | 192 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1360+14077C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397861 | ||||||
| chr4:48397894
|
C | G | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+14110C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397894 | ||||||
| chr4:48397895
|
G | C | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1360+14111G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397895 | ||||||
| chr4:48397978
|
A | G | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1360+14194A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397978 | ||||||
| chr4:48398024
|
C | T | 1 | a0001c0001t0013g0245 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1360+14240C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398024 | ||||||
| chr4:48398133
|
A | G | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+14349A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398133 | ||||||
| chr4:48398146
|
T | C | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+14362T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398146 | ||||||
| chr4:48398154
|
G | C | 1 | a0004c0009t0002g0331 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1360+14370G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398154 | ||||||
| chr4:48398470
|
C | T | 1 | a0001c0002t0005g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1360+14686C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398470 | ||||||
| chr4:48398707
|
G | A | 1 | a0001c0001t0003g0202 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1360+14923G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398707 | ||||||
| chr4:48398708
|
C | A | 1 | a0001c0001t0003g0202 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1360+14924C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398708 | ||||||
| chr4:48398781
|
G | A | 1 | a0001c0001t0003g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1360+14997G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398781 | ||||||
| chr4:48398876
|
T | C | 3 | a0001c0001t0003g0182a0001c0001t0003g0202a0001c0001t0003g0217 | 3 | HG01516.hp1 NA18943.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1360+15092T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398876 | ||||||
| chr4:48398894
|
C | G | 192 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1360+15110C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398894 | ||||||
| chr4:48398941
|
G | A | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+15157G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398941 | ||||||
| chr4:48398967
|
T | A | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1360+15183T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398967 | ||||||
| chr4:48398976
|
G | C | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+15192G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398976 | ||||||
| chr4:48398998
|
G | C | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+15214G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398998 | ||||||
| chr4:48399126
|
C | G | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1360+15342C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399126 | ||||||
| chr4:48399132
|
A | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+15348A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399132 | ||||||
| chr4:48399152
|
C | A | 4 | a0001c0002t0009g0171a0001c0002t0009g0172a0001c0002t0009g0204others(1): Show | 4 | HG00741.hp2 HG01074.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360+15368C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399152 | ||||||
| chr4:48399266
|
T | C | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+15482T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399266 | ||||||
| chr4:48399400
|
T | G | 12 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(9): Show | 13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1360+15616T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399400 | ||||||
| chr4:48399622
|
A | G | 2 | a0001c0003t0012g0221a0001c0003t0012g0222 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1360+15838A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399622 | ||||||
| chr4:48399894
|
G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+16110G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399894 | ||||||
| chr4:48399897
|
C | T | 1 | a0001c0001t0001g0039 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1360+16113C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399897 | ||||||
| chr4:48400031
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1360+16247A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400031 | ||||||
| chr4:48400377
|
G | A | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(335): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1360+16593G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400377 | ||||||
| chr4:48400388
|
CT | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 135 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.1360+16630delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | |||||
| chr4:48400388
|
CTTTTTTT | C | 8 | a0001c0001t0002g0235a0001c0001t0002g0247a0001c0001t0002g0257others(5): Show | 8 | HG01243.hp2 HG01346.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1360+16624_1360+16 others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | |||||
| chr4:48400388
|
CTTTTTTT others(1): Show |
C | 147 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(144): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1360+16623_1360+16 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | |||||
| chr4:48400388
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+16620_1360+16 others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | |||||
| chr4:48400388
|
CTTTTTTT others(5): Show |
C | 25 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(22): Show | 26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1360+16619_1360+16 others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | |||||
| chr4:48400608
|
G | T | 1 | a0001c0001t0002g0284 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1360+16824G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400608 | ||||||
| chr4:48400746
|
A | T | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+16962A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400746 | ||||||
| chr4:48400766
|
CGTTT | C | 14 | a0001c0001t0004g0319a0001c0002t0005g0005a0001c0002t0005g0173others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+16999_1360+17 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400766 | |||||
| chr4:48400898
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1360+17114G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400898 | ||||||
| chr4:48400923
|
C | T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+17139C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400923 | ||||||
| chr4:48401006
|
G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+17222G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401006 | ||||||
| chr4:48401103
|
G | C | 1 | a0001c0001t0007g0330 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1360+17319G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401103 | ||||||
| chr4:48401284
|
A | G | 1 | a0001c0002t0009g0172 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1360+17500A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401284 | ||||||
| chr4:48401295
|
T | G | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+17511T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401295 | ||||||
| chr4:48401388
|
A | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1360+17604A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401388 | ||||||
| chr4:48401403
|
G | T | 1 | a0001c0001t0001g0015 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1360+17619G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401403 | ||||||
| chr4:48401419
|
G | C | 2 | a0001c0001t0002g0230a0001c0001t0002g0291 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1360+17635G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401419 | ||||||
| chr4:48401442
|
A | G | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+17658A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401442 | ||||||
| chr4:48401523
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+17739G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401523 | ||||||
| chr4:48401906
|
T | C | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1360+18122T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401906 | ||||||
| chr4:48402046
|
T | C | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-18079T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402046 | ||||||
| chr4:48402050
|
A | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0113 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1361-18075A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402050 | ||||||
| chr4:48402057
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1361-18068G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402057 | ||||||
| chr4:48402077
|
G | A | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-18048G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402077 | ||||||
| chr4:48402199
|
A | AT | 12 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(9): Show | 13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1361-17926_1361-17 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402199 | ||||||
| chr4:48402200
|
A | AT | 152 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(149): Show | 155 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1361-17911dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48402200 | |||||
| chr4:48402200
|
A | T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-17925A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402200 | ||||||
| chr4:48402224
|
C | T | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-17901C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402224 | ||||||
| chr4:48402225
|
G | A | 1 | a0001c0001t0004g0258 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1361-17900G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402225 | ||||||
| chr4:48402246
|
T | C | 2 | a0001c0001t0002g0288a0001c0001t0002g0292 | 2 | NA18977.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1361-17879T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402246 | ||||||
| chr4:48402248
|
T | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-17877T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402248 | ||||||
| chr4:48402323
|
T | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-17802T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402323 | ||||||
| chr4:48402549
|
C | G | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-17576C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402549 | ||||||
| chr4:48402765
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-17360C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402765 | ||||||
| chr4:48402845
|
T | A | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-17280T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402845 | ||||||
| chr4:48402908
|
G | A | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-17217G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402908 | ||||||
| chr4:48403159
|
C | T | 1 | a0001c0001t0001g0148 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1361-16966C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403159 | ||||||
| chr4:48403361
|
G | C | 1 | a0001c0001t0001g0050 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1361-16764G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403361 | ||||||
| chr4:48403374
|
A | C | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-16751A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403374 | ||||||
| chr4:48403417
|
C | T | 12 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(9): Show | 13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1361-16708C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403417 | ||||||
| chr4:48403465
|
A | G | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-16660A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403465 | ||||||
| chr4:48403612
|
C | T | 1 | a0001c0006t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1361-16513C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403612 | ||||||
| chr4:48403626
|
C | T | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-16499C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403626 | ||||||
| chr4:48403639
|
G | A | 1 | a0001c0001t0001g0149 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1361-16486G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403639 | ||||||
| chr4:48403720
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1361-16405T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403720 | ||||||
| chr4:48403720
|
T | G | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-16405T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403720 | ||||||
| chr4:48403846
|
G | A | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-16279G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403846 | ||||||
| chr4:48403892
|
G | A | 1 | a0001c0002t0005g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1361-16233G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403892 | ||||||
| chr4:48404074
|
T | C | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-16051T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404074 | ||||||
| chr4:48404147
|
A | T | 6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-15978A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404147 | ||||||
| chr4:48404247
|
A | C | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-15878A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404247 | ||||||
| chr4:48404413
|
T | G | 6 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(3): Show | 6 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-15712T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404413 | ||||||
| chr4:48404419
|
C | CT | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-15704dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48404419 | |||||
| chr4:48404555
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1361-15570A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404555 | ||||||
| chr4:48404674
|
G | T | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-15451G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404674 | ||||||
| chr4:48404819
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1361-15306A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404819 | ||||||
| chr4:48404827
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1361-15298C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404827 | ||||||
| chr4:48404956
|
C | T | 1 | a0001c0001t0002g0287 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1361-15169C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404956 | ||||||
| chr4:48405172
|
C | T | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-14953C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405172 | ||||||
| chr4:48405272
|
C | T | 1 | a0001c0001t0002g0333 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1361-14853C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405272 | ||||||
| chr4:48405335
|
A | G | 1 | a0001c0001t0002g0333 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1361-14790A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405335 | ||||||
| chr4:48405359
|
CCTTTTTG others(6): Show |
C | 1 | a0001c0001t0002g0313 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1361-14759_1361-14 others(19): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48405359 | |||||
| chr4:48405527
|
T | C | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-14598T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405527 | ||||||
| chr4:48405595
|
A | G | 2 | a0001c0003t0012g0221a0001c0003t0012g0222 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1361-14530A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405595 | ||||||
| chr4:48405656
|
A | C | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1361-14469A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405656 | ||||||
| chr4:48405758
|
G | A | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-14367G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405758 | ||||||
| chr4:48405969
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1361-14156G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405969 | ||||||
| chr4:48406024
|
C | T | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1361-14101C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406024 | ||||||
| chr4:48406179
|
A | G | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-13946A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406179 | ||||||
| chr4:48406296
|
T | C | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-13829T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406296 | ||||||
| chr4:48406461
|
T | C | 12 | a0001c0001t0001g0068a0001c0001t0001g0076a0001c0001t0001g0101others(9): Show | 12 | HG00280.hp2 HG01070.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1361-13664T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406461 | ||||||
| chr4:48406472
|
A | G | 1 | a0001c0001t0002g0300 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1361-13653A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406472 | ||||||
| chr4:48406516
|
T | G | 1 | a0001c0001t0028g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1361-13609T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406516 | ||||||
| chr4:48406518
|
T | G | 8 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(5): Show | 8 | HG01070.hp1 HG01433.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1361-13607T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406518 | ||||||
| chr4:48406525
|
CT | C | 19 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0048others(16): Show | 19 | HG00558.hp1 HG01169.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1361-13580delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48406525 | |||||
| chr4:48406525
|
CTT | C | 23 | a0001c0001t0001g0159a0001c0001t0003g0194a0001c0002t0005g0173others(20): Show | 23 | HG00741.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1361-13581_1361-13 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48406525 | |||||
| chr4:48406525
|
CTTT | C | 147 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(144): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1361-13582_1361-13 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48406525 | |||||
| chr4:48406525
|
CTTTT | C | 11 | a0001c0001t0002g0249a0001c0001t0002g0271a0001c0001t0002g0277others(8): Show | 11 | HG01070.hp2 HG01256.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-13583_1361-13 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48406525 | |||||
| chr4:48406527
|
T | C | 2 | a0001c0003t0012g0221a0001c0003t0012g0222 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1361-13598T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406527 | ||||||
| chr4:48406528
|
T | C | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-13597T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406528 | ||||||
| chr4:48406529
|
T | C | 4 | a0001c0003t0006g0218a0001c0003t0006g0219a0001c0003t0006g0220others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-13596T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406529 | ||||||
| chr4:48406582
|
C | A | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-13543C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406582 | ||||||
| chr4:48406609
|
A | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-13516A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406609 | ||||||
| chr4:48406725
|
G | A | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-13400G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406725 | ||||||
| chr4:48406804
|
A | G | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-13321A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406804 | ||||||
| chr4:48406894
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1361-13231T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406894 | ||||||
| chr4:48407024
|
A | G | 1 | a0007c0005t0001g0104 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1361-13101A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407024 | ||||||
| chr4:48407146
|
T | G | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-12979T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407146 | ||||||
| chr4:48407176
|
C | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(335): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1361-12949C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407176 | ||||||
| chr4:48407194
|
C | T | 1 | a0003c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1361-12931C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407194 | ||||||
| chr4:48407255
|
T | C | 3 | a0001c0001t0002g0250a0001c0001t0002g0261a0001c0001t0002g0268 | 3 | NA18974.hp2 NA19065.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1361-12870T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407255 | ||||||
| chr4:48407270
|
T | G | 158 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(155): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1361-12855T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407270 | ||||||
| chr4:48407298
|
C | T | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-12827C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407298 | ||||||
| chr4:48407324
|
C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-12801C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407324 | ||||||
| chr4:48407330
|
T | C | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-12795T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407330 | ||||||
| chr4:48407346
|
C | T | 193 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(190): Show | 197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1361-12779C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407346 | ||||||
| chr4:48407538
|
A | G | 64 | a0001c0001t0001g0008a0001c0001t0001g0044a0001c0001t0001g0048others(61): Show | 64 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1361-12587A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407538 | ||||||
| chr4:48407748
|
T | C | 1 | a0001c0001t0003g0195 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1361-12377T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407748 | ||||||
| chr4:48407954
|
A | G | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-12171A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407954 | ||||||
| chr4:48408098
|
C | T | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-12027C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408098 | ||||||
| chr4:48408184
|
G | A | 2 | a0001c0001t0003g0182a0001c0001t0003g0202 | 2 | HG01516.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1361-11941G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408184 | ||||||
| chr4:48408200
|
C | T | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-11925C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408200 | ||||||
| chr4:48408229
|
G | C | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-11896G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408229 | ||||||
| chr4:48408333
|
A | C | 1 | a0001c0003t0006g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1361-11792A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408333 | ||||||
| chr4:48408361
|
C | T | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-11764C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408361 | ||||||
| chr4:48408437
|
A | G | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-11688A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408437 | ||||||
| chr4:48408446
|
G | A | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-11679G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408446 | ||||||
| chr4:48408530
|
C | CA | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(116): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1361-11575dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | |||||
| chr4:48408530
|
C | CAA | 104 | a0001c0001t0001g0061a0001c0001t0001g0095a0001c0001t0001g0141others(101): Show | 106 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1361-11576_1361-11 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | |||||
| chr4:48408530
|
C | CAAA | 57 | a0001c0001t0001g0225a0001c0001t0002g0257a0001c0001t0002g0272others(54): Show | 58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1361-11577_1361-11 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | |||||
| chr4:48408530
|
C | CAAAA | 14 | a0001c0001t0003g0166a0001c0001t0003g0202a0001c0002t0005g0005others(11): Show | 15 | HG00733.hp1 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-11578_1361-11 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | |||||
| chr4:48408530
|
CA | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0020others(4): Show | 7 | HG01255.hp1 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-11575delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | |||||
| chr4:48408672
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1361-11453A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408672 | ||||||
| chr4:48408687
|
T | A | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-11438T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408687 | ||||||
| chr4:48408725
|
C | G | 6 | a0001c0002t0005g0005a0001c0002t0005g0174a0001c0002t0005g0175others(3): Show | 7 | HG01069.hp2 HG01109.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-11400C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408725 | ||||||
| chr4:48408904
|
G | C | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-11221G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408904 | ||||||
| chr4:48408932
|
C | T | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-11193C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408932 | ||||||
| chr4:48409043
|
T | C | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-11082T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409043 | ||||||
| chr4:48409068
|
A | G | 1 | a0001c0001t0010g0089 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1361-11057A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409068 | ||||||
| chr4:48409196
|
A | G | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-10929A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409196 | ||||||
| chr4:48409287
|
A | AT | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-10829dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48409287 | |||||
| chr4:48409317
|
A | T | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-10808A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409317 | ||||||
| chr4:48409470
|
A | C | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-10655A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409470 | ||||||
| chr4:48409514
|
C | T | 1 | a0001c0001t0002g0291 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1361-10611C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409514 | ||||||
| chr4:48409774
|
C | T | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-10351C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409774 | ||||||
| chr4:48409837
|
T | C | 2 | a0001c0001t0002g0289a0001c0001t0007g0337 | 2 | HG02602.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1361-10288T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409837 | ||||||
| chr4:48409901
|
A | AATG | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-10223_1361-10 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48409901 | |||||
| chr4:48409958
|
T | G | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-10167T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409958 | ||||||
| chr4:48409992
|
G | A | 4 | a0001c0001t0002g0285a0001c0001t0002g0286a0001c0001t0002g0328others(1): Show | 4 | HG01358.hp1 HG01928.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-10133G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409992 | ||||||
| chr4:48410141
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-9984G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410141 | ||||||
| chr4:48410279
|
GT | G | 23 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(20): Show | 23 | HG01167.hp1 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1361-9832delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48410279 | |||||
| chr4:48410436
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-9689G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410436 | ||||||
| chr4:48410522
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1361-9603C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410522 | ||||||
| chr4:48410580
|
C | T | 1 | a0001c0001t0002g0284 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1361-9545C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410580 | ||||||
| chr4:48410726
|
T | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0226 | 3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1361-9399T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410726 | ||||||
| chr4:48410775
|
G | A | 1 | a0001c0001t0002g0249 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1361-9350G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410775 | ||||||
| chr4:48410826
|
C | A | 12 | a0001c0001t0029g0163a0001c0003t0006g0028a0001c0003t0006g0029others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1361-9299C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410826 | ||||||
| chr4:48410974
|
C | T | 1 | a0002c0011t0020g0263 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1361-9151C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410974 | ||||||
| chr4:48410980
|
C | T | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-9145C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410980 | ||||||
| chr4:48411033
|
G | T | 5 | a0001c0001t0004g0320a0001c0001t0004g0323a0001c0001t0004g0324others(2): Show | 5 | HG02074.hp1 NA18950.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1361-9092G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411033 | ||||||
| chr4:48411186
|
T | A | 1 | a0001c0002t0005g0174 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1361-8939T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411186 | ||||||
| chr4:48411231
|
A | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-8894A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411231 | ||||||
| chr4:48411281
|
C | T | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-8844C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411281 | ||||||
| chr4:48411494
|
A | G | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-8631A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411494 | ||||||
| chr4:48411581
|
C | T | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-8544C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411581 | ||||||
| chr4:48411603
|
G | GT | 9 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361-8510dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48411603 | |||||
| chr4:48411603
|
GT | G | 156 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(153): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1361-8510delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48411603 | |||||
| chr4:48411624
|
T | A | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-8501T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411624 | ||||||
| chr4:48411769
|
A | AT | 9 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361-8349dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48411769 | |||||
| chr4:48411783
|
G | A | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1361-8342G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411783 | ||||||
| chr4:48411902
|
T | C | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-8223T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411902 | ||||||
| chr4:48412017
|
A | AT | 115 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-8106dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412017 | |||||
| chr4:48412038
|
C | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-8087C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412038 | ||||||
| chr4:48412157
|
A | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-7968A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412157 | ||||||
| chr4:48412193
|
A | G | 1 | a0006c0008t0001g0120 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1361-7932A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412193 | ||||||
| chr4:48412212
|
A | G | 1 | a0001c0001t0004g0327 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1361-7913A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412212 | ||||||
| chr4:48412311
|
GGGTGGAG others(214): Show |
G | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-7810_1361-759 others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412311 | |||||
| chr4:48412325
|
A | C | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-7800A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412325 | ||||||
| chr4:48412364
|
G | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-7761G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412364 | ||||||
| chr4:48412365
|
T | TAC | 19 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0045others(16): Show | 19 | HG00323.hp1 HG00733.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1361-7710_1361-770 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
T | TACAC | 7 | a0001c0001t0001g0018a0001c0001t0001g0081a0001c0001t0001g0087others(4): Show | 7 | HG01358.hp2 HG01361.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-7712_1361-770 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
T | TACACAC | 4 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0148others(1): Show | 4 | HG02809.hp1 NA18964.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1361-7714_1361-770 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
T | TACACACA others(3): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18995.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1361-7718_1361-770 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
TAC | T | 39 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(36): Show | 41 | HG00280.hp2 HG00609.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1361-7710_1361-770 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
TACAC | T | 21 | a0001c0001t0001g0011a0001c0001t0001g0046a0001c0001t0001g0051others(18): Show | 21 | HG00140.hp2 HG00642.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.1361-7712_1361-770 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
TACACAC | T | 6 | a0001c0001t0001g0075a0001c0001t0001g0124a0001c0001t0001g0127others(3): Show | 6 | HG01433.hp2 HG02004.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.1361-7714_1361-770 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
TACACACA others(1): Show |
T | 14 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0016others(11): Show | 15 | HG01167.hp1 HG02040.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-7716_1361-770 others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1361-7718_1361-770 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0035a0001c0001t0023g0031a0001c0001t0027g0181 | 3 | HG02630.hp2 HG03139.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1361-7720_1361-770 others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
TACACACA others(7): Show |
T | 12 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0034others(9): Show | 13 | HG02074.hp2 HG02735.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.1361-7722_1361-770 others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
TACACACA others(9): Show |
T | 3 | a0001c0001t0001g0020a0001c0001t0001g0095a0001c0001t0025g0043 | 3 | HG03098.hp2 HG03834.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.1361-7724_1361-770 others(20): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412365
|
TACACACA others(11): Show |
T | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | HG01070.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1361-7726_1361-770 others(22): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | |||||
| chr4:48412387
|
CACACACA others(23): Show |
C | 5 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0307others(2): Show | 5 | HG01109.hp1 HG01255.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1361-7737_1361-770 others(34): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412387 | ||||||
| chr4:48412389
|
CACACACA others(21): Show |
C | 3 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0021g0242 | 3 | HG02004.hp1 HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1361-7735_1361-770 others(32): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412389 | ||||||
| chr4:48412390
|
ACACACAC others(25): Show |
A | 11 | a0001c0001t0004g0251a0001c0001t0004g0260a0001c0001t0004g0267others(8): Show | 11 | HG02074.hp1 NA18939.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361-7733_1361-770 others(36): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412390 | |||||
| chr4:48412391
|
CACACACA others(19): Show |
C | 96 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(93): Show | 98 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1361-7733_1361-770 others(30): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412391 | ||||||
| chr4:48412403
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0003g0210 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1361-7721_1361-770 others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412403 | ||||||
| chr4:48412405
|
CACACACA others(5): Show |
C | 2 | a0001c0001t0003g0168a0001c0001t0016g0340 | 2 | HG02615.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1361-7719_1361-770 others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412405 | ||||||
| chr4:48412407
|
C | A | 4 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1361-7718C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412407 | ||||||
| chr4:48412407
|
C | CAA | 4 | a0001c0003t0006g0032a0001c0003t0006g0223a0001c0003t0012g0221others(1): Show | 4 | HG02615.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-7717_1361-771 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412407 | |||||
| chr4:48412407
|
C | CACAA | 3 | a0001c0003t0006g0218a0001c0003t0006g0219a0001c0003t0006g0220 | 3 | HG02145.hp2 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1361-7715_1361-771 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412407 | |||||
| chr4:48412407
|
CACACACA others(3): Show |
C | 7 | a0001c0001t0003g0166a0001c0001t0003g0187a0001c0001t0003g0188others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-7717_1361-770 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412407 | ||||||
| chr4:48412409
|
C | A | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-7716C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412409 | ||||||
| chr4:48412409
|
CACACACA others(1): Show |
C | 7 | a0001c0001t0003g0167a0001c0001t0003g0182a0001c0001t0003g0184others(4): Show | 7 | HG00280.hp1 HG00738.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-7715_1361-770 others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412409 | ||||||
| chr4:48412411
|
CACACAT | C | 17 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0185others(14): Show | 18 | HG00642.hp2 HG00735.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1361-7713_1361-770 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412411 | ||||||
| chr4:48412413
|
CACAT | C | 8 | a0001c0001t0003g0165a0001c0001t0003g0169a0001c0001t0003g0170others(5): Show | 8 | HG00323.hp2 HG01243.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1361-7711_1361-770 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412413 | ||||||
| chr4:48412420
|
CCT | C | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-7688_1361-768 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412420 | |||||
| chr4:48412426
|
T | C | 11 | a0001c0001t0004g0251a0001c0001t0004g0260a0001c0001t0004g0267others(8): Show | 11 | HG02074.hp1 NA18939.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361-7699T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412426 | ||||||
| chr4:48412470
|
A | G | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-7655A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412470 | ||||||
| chr4:48412686
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1361-7439C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412686 | ||||||
| chr4:48412687
|
G | A | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1361-7438G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412687 | ||||||
| chr4:48412955
|
C | T | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-7170C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412955 | ||||||
| chr4:48413142
|
C | T | 1 | a0001c0001t0028g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1361-6983C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413142 | ||||||
| chr4:48413209
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1361-6916T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413209 | ||||||
| chr4:48413227
|
CA | C | 8 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(5): Show | 8 | HG01167.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1361-6883delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48413227 | |||||
| chr4:48413227
|
CAA | C | 75 | a0001c0001t0002g0227a0001c0001t0002g0230a0001c0001t0002g0235others(72): Show | 77 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1361-6884_1361-688 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48413227 | |||||
| chr4:48413227
|
CAAA | C | 108 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(105): Show | 110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.1361-6885_1361-688 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48413227 | |||||
| chr4:48413242
|
A | G | 2 | a0001c0001t0003g0187a0001c0001t0003g0210 | 2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1361-6883A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413242 | ||||||
| chr4:48413311
|
A | G | 1 | a0001c0001t0003g0211 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1361-6814A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413311 | ||||||
| chr4:48413345
|
C | T | 3 | a0001c0001t0002g0243a0001c0001t0002g0308a0001c0001t0002g0311 | 3 | HG01070.hp2 HG01071.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1361-6780C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413345 | ||||||
| chr4:48413353
|
C | A | 1 | a0001c0001t0008g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1361-6772C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413353 | ||||||
| chr4:48413491
|
C | T | 1 | a0001c0001t0003g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1361-6634C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413491 | ||||||
| chr4:48413558
|
A | T | 1 | a0001c0001t0001g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1361-6567A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413558 | ||||||
| chr4:48413623
|
G | T | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-6502G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413623 | ||||||
| chr4:48413818
|
A | G | 1 | a0001c0001t0002g0287 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1361-6307A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413818 | ||||||
| chr4:48414235
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1361-5890T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414235 | ||||||
| chr4:48414411
|
A | G | 2 | a0001c0003t0006g0028a0001c0003t0006g0029 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1361-5714A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414411 | ||||||
| chr4:48414460
|
G | A | 1 | a0001c0002t0031g0178 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1361-5665G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414460 | ||||||
| chr4:48414550
|
A | AT | 6 | a0001c0001t0001g0059a0001c0001t0001g0102a0001c0001t0001g0139others(3): Show | 6 | HG01496.hp2 HG01981.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-5555dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | |||||
| chr4:48414550
|
AT | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0034others(16): Show | 20 | HG01069.hp1 HG02074.hp2 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.1361-5555delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | |||||
| chr4:48414550
|
ATT | A | 7 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(4): Show | 7 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-5556_1361-555 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | |||||
| chr4:48414550
|
ATTT | A | 10 | a0001c0001t0029g0163a0001c0003t0006g0028a0001c0003t0006g0029others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1361-5557_1361-555 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | |||||
| chr4:48414550
|
ATTTTTTT | A | 156 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(153): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1361-5561_1361-555 others(11): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | |||||
| chr4:48414568
|
TTTA | T | 10 | a0001c0002t0005g0005a0001c0002t0005g0174a0001c0002t0005g0175others(7): Show | 11 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361-5552_1361-555 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414568 | |||||
| chr4:48414673
|
G | A | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-5452G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414673 | ||||||
| chr4:48414700
|
C | T | 11 | a0001c0002t0005g0005a0001c0002t0005g0174a0001c0002t0005g0175others(8): Show | 12 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1361-5425C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414700 | ||||||
| chr4:48414714
|
C | T | 37 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(34): Show | 38 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1361-5411C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414714 | ||||||
| chr4:48414805
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1361-5320G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414805 | ||||||
| chr4:48414828
|
G | A | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-5297G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414828 | ||||||
| chr4:48414855
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1361-5270A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414855 | ||||||
| chr4:48414858
|
T | C | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-5267T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414858 | ||||||
| chr4:48414973
|
G | C | 2 | a0001c0001t0002g0297a0001c0001t0002g0298 | 2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1361-5152G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414973 | ||||||
| chr4:48415008
|
G | A | 1 | a0001c0001t0011g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1361-5117G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415008 | ||||||
| chr4:48415058
|
C | A | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-5067C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415058 | ||||||
| chr4:48415244
|
A | T | 184 | a0001c0001t0001g0105a0001c0001t0002g0006a0001c0001t0002g0007others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1361-4881A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415244 | ||||||
| chr4:48415325
|
C | T | 1 | a0001c0001t0003g0168 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1361-4800C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415325 | ||||||
| chr4:48415335
|
T | C | 1 | a0001c0001t0003g0168 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1361-4790T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415335 | ||||||
| chr4:48415379
|
A | G | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-4746A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415379 | ||||||
| chr4:48415385
|
C | T | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-4740C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415385 | ||||||
| chr4:48415386
|
A | G | 195 | a0001c0001t0001g0139a0001c0001t0001g0154a0001c0001t0001g0155others(192): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1361-4739A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415386 | ||||||
| chr4:48415390
|
A | G | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-4735A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415390 | ||||||
| chr4:48415446
|
A | G | 2 | a0001c0003t0006g0028a0001c0003t0006g0029 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1361-4679A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415446 | ||||||
| chr4:48415483
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1361-4642C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415483 | ||||||
| chr4:48415513
|
T | C | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-4612T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415513 | ||||||
| chr4:48415517
|
C | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1361-4608C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415517 | ||||||
| chr4:48415562
|
C | A | 104 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(101): Show | 106 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1361-4563C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415562 | ||||||
| chr4:48415587
|
G | T | 2 | a0001c0001t0002g0230a0001c0001t0002g0291 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1361-4538G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415587 | ||||||
| chr4:48415622
|
G | A | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-4503G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415622 | ||||||
| chr4:48415641
|
G | A | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-4484G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415641 | ||||||
| chr4:48415763
|
C | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-4362C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415763 | ||||||
| chr4:48415820
|
C | A | 1 | a0001c0006t0001g0096 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1361-4305C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415820 | ||||||
| chr4:48415841
|
C | G | 8 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(5): Show | 8 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1361-4284C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415841 | ||||||
| chr4:48415877
|
C | T | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-4248C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415877 | ||||||
| chr4:48415878
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG01167.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-4247G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415878 | ||||||
| chr4:48415940
|
G | C | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-4185G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415940 | ||||||
| chr4:48415942
|
A | G | 8 | a0001c0001t0002g0234a0001c0001t0002g0304a0001c0001t0002g0315others(5): Show | 8 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1361-4183A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415942 | ||||||
| chr4:48416036
|
G | A | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-4089G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416036 | ||||||
| chr4:48416043
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1361-4082G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416043 | ||||||
| chr4:48416072
|
G | A | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-4053G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416072 | ||||||
| chr4:48416076
|
G | GT | 157 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(154): Show | 160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-4043dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48416076 | |||||
| chr4:48416160
|
A | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-3965A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416160 | ||||||
| chr4:48416166
|
A | C | 1 | a0001c0001t0002g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1361-3959A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416166 | ||||||
| chr4:48416168
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1361-3957G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416168 | ||||||
| chr4:48416252
|
G | C | 2 | a0001c0003t0012g0221a0001c0003t0012g0222 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1361-3873G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416252 | ||||||
| chr4:48416264
|
G | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-3861G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416264 | ||||||
| chr4:48416369
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0159 | 3 | HG01167.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1361-3756G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416369 | ||||||
| chr4:48416468
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1361-3657G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416468 | ||||||
| chr4:48416469
|
A | G | 1 | a0001c0001t0003g0193 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1361-3656A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416469 | ||||||
| chr4:48416490
|
A | G | 1 | a0001c0003t0006g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1361-3635A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416490 | ||||||
| chr4:48416514
|
A | C | 1 | a0001c0001t0003g0212 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1361-3611A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416514 | ||||||
| chr4:48416595
|
A | G | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-3530A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416595 | ||||||
| chr4:48416608
|
G | A | 13 | a0001c0001t0029g0163a0001c0002t0030g0205a0001c0003t0006g0028others(10): Show | 13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1361-3517G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416608 | ||||||
| chr4:48416609
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1361-3516C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416609 | ||||||
| chr4:48416610
|
G | A | 13 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(10): Show | 14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-3515G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416610 | ||||||
| chr4:48416735
|
A | G | 2 | a0001c0001t0003g0004a0001c0001t0003g0196 | 3 | NA18957.hp2 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1361-3390A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416735 | ||||||
| chr4:48416762
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1361-3363A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416762 | ||||||
| chr4:48416766
|
C | T | 1 | a0001c0001t0003g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1361-3359C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416766 | ||||||
| chr4:48416852
|
C | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-3273C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416852 | ||||||
| chr4:48416915
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1361-3210T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416915 | ||||||
| chr4:48416984
|
G | A | 1 | a0001c0003t0006g0030 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1361-3141G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416984 | ||||||
| chr4:48417084
|
C | A | 114 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(111): Show | 116 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1361-3041C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417084 | ||||||
| chr4:48417099
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1361-3026A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417099 | ||||||
| chr4:48417113
|
T | G | 1 | a0001c0003t0006g0032 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1361-3012T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417113 | ||||||
| chr4:48417116
|
T | TAAAG | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-3006_1361-300 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48417116 | |||||
| chr4:48417239
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1361-2886A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417239 | ||||||
| chr4:48417284
|
C | A | 28 | a0001c0001t0002g0007a0001c0001t0002g0229a0001c0001t0002g0243others(25): Show | 29 | HG00099.hp2 HG00408.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1361-2841C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417284 | ||||||
| chr4:48417284
|
C | G | 1 | a0001c0001t0002g0227 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1361-2841C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417284 | ||||||
| chr4:48417348
|
G | A | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-2777G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417348 | ||||||
| chr4:48417493
|
G | C | 179 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(176): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1361-2632G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417493 | ||||||
| chr4:48417529
|
C | T | 1 | a0001c0001t0002g0302 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1361-2596C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417529 | ||||||
| chr4:48417606
|
A | G | 1 | a0001c0001t0023g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-2519A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417606 | ||||||
| chr4:48417642
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1361-2483C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417642 | ||||||
| chr4:48417699
|
C | T | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-2426C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417699 | ||||||
| chr4:48417735
|
G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-2390G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417735 | ||||||
| chr4:48417765
|
A | G | 1 | a0001c0001t0002g0328 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1361-2360A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417765 | ||||||
| chr4:48417907
|
G | A | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1361-2218G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417907 | ||||||
| chr4:48417936
|
T | C | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-2189T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417936 | ||||||
| chr4:48417958
|
T | C | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-2167T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417958 | ||||||
| chr4:48418071
|
T | C | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-2054T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418071 | ||||||
| chr4:48418074
|
TTTC | T | 110 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0228others(107): Show | 112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-2035_1361-203 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418074 | |||||
| chr4:48418074
|
TTTCTTC | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0226 | 3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1361-2038_1361-203 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418074 | |||||
| chr4:48418138
|
CCTTCTTT others(10): Show |
C | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-1984_1361-196 others(21): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418138 | |||||
| chr4:48418163
|
T | C | 1 | a0001c0001t0018g0290 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1361-1962T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418163 | ||||||
| chr4:48418168
|
CT | C | 12 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(9): Show | 13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1361-1945delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418168 | |||||
| chr4:48418393
|
T | C | 41 | a0001c0001t0003g0004a0001c0001t0003g0164a0001c0001t0003g0165others(38): Show | 42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-1732T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418393 | ||||||
| chr4:48418541
|
A | G | 1 | a0001c0001t0027g0181 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-1584A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418541 | ||||||
| chr4:48418558
|
T | A | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-1567T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418558 | ||||||
| chr4:48418602
|
C | T | 1 | a0001c0001t0021g0242 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1361-1523C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418602 | ||||||
| chr4:48418603
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-1522G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418603 | ||||||
| chr4:48418614
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1361-1511T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418614 | ||||||
| chr4:48418851
|
AGT | A | 111 | a0001c0001t0001g0073a0001c0001t0002g0006a0001c0001t0002g0007others(108): Show | 113 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.1361-1261_1361-126 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418851 | |||||
| chr4:48419012
|
A | T | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1361-1113A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419012 | ||||||
| chr4:48419029
|
C | T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-1096C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419029 | ||||||
| chr4:48419109
|
C | CT | 153 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(150): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1361-1005dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48419109 | |||||
| chr4:48419142
|
G | A | 1 | a0001c0001t0002g0335 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1361-983G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419142 | ||||||
| chr4:48419170
|
C | G | 1 | a0001c0001t0003g0182 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1361-955C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419170 | ||||||
| chr4:48419223
|
C | G | 1 | a0001c0001t0016g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-902C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419223 | ||||||
| chr4:48419350
|
C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-775C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419350 | ||||||
| chr4:48419355
|
C | T | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-770C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419355 | ||||||
| chr4:48419362
|
C | G | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-763C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419362 | ||||||
| chr4:48419384
|
G | A | 26 | a0001c0001t0029g0163a0001c0002t0005g0005a0001c0002t0005g0173others(23): Show | 27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1361-741G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419384 | ||||||
| chr4:48419469
|
C | T | 11 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-656C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419469 | ||||||
| chr4:48419499
|
C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-626C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419499 | ||||||
| chr4:48419576
|
G | GT | 14 | a0001c0002t0005g0005a0001c0002t0005g0173a0001c0002t0005g0174others(11): Show | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-543dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48419576 | |||||
| chr4:48419697
|
A | G | 1 | a0001c0003t0006g0029 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1361-428A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419697 | ||||||
| chr4:48419772
|
A | G | 1 | a0001c0001t0004g0295 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1361-353A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419772 | ||||||
| chr4:48419779
|
C | G | 9 | a0001c0003t0006g0028a0001c0003t0006g0029a0001c0003t0006g0030others(6): Show | 9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361-346C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419779 | ||||||
| chr4:48419892
|
A | G | 1 | a0001c0002t0030g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-233A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419892 | ||||||
| chr4:48420503
|
T | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1679+60T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420503 | ||||||
| chr4:48420570
|
G | T | 9 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(6): Show | 9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679+127G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420570 | ||||||
| chr4:48420745
|
C | T | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1679+302C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420745 | ||||||
| chr4:48420751
|
T | G | 194 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1679+308T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420751 | ||||||
| chr4:48420828
|
T | C | 71 | a0001c0001t0002g0006a0001c0001t0002g0228a0001c0001t0002g0239others(68): Show | 72 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(69): Show |
intron_variant | MODIFIER | c.1679+385T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420828 | ||||||
| chr4:48420860
|
C | A | 1 | a0001c0001t0004g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1679+417C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420860 | ||||||
| chr4:48420935
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1679+492A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420935 | ||||||
| chr4:48421007
|
TTTTTGTT others(4): Show |
T | 1 | a0001c0001t0001g0139 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1679+581_1679+591d others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 48421007 | |||||
| chr4:48421057
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1679+614C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421057 | ||||||
| chr4:48421071
|
G | A | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1679+628G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421071 | ||||||
| chr4:48421084
|
T | C | 183 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0227others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1679+641T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421084 | ||||||
| chr4:48421095
|
A | C | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679+652A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421095 | ||||||
| chr4:48421174
|
C | G | 1 | a0001c0003t0006g0220 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1679+731C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421174 | ||||||
| chr4:48421219
|
C | G | 2 | a0001c0003t0006g0028a0001c0003t0006g0029 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1679+776C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421219 | ||||||
| chr4:48421713
|
A | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0020others(4): Show | 7 | HG01255.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1680-298A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421713 | ||||||
| chr4:48421808
|
C | G | 5 | a0001c0001t0002g0227a0001c0001t0002g0235a0001c0004t0002g0236others(2): Show | 5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1680-203C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421808 |