Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 92105 |
|---|---|
| ensemblid | ENSG00000149262.19 |
| hgncid | 25048 |
| symbol | INTS4 |
| name | integrator complex subunit 4 |
| refseq_nuc | NM_033547.4 |
| refseq_prot | NP_291025.3 |
| ensembl_nuc | ENST00000534064.6 |
| ensembl_prot | ENSP00000434466.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 77878720 |
| end | 77994668 |
| strand | - |
| ver | v1.2 |
| region | chr11:77878720-77994668 |
| region5000 | chr11:77873720-77999668 |
| regionname0 | INTS4_chr11_77878720_77994668 |
| regionname5000 | INTS4_chr11_77873720_77999668 |
| 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 | 963 | 351 | 73 | 61 | 168 | 16 | 31 | 128 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0002 | 0/0 | 963 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0003 | 0/0 | 963 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0004 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0005 | 0/0 | 963 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0006 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| 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 | 2892 | 270 | 50 | 49 | 136 | 12 | 21 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| c0002 | 0/0 | 2892 | 74 | 16 | 12 | 32 | 4 | 10 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| c0003 | 0/0 | 2892 | 6 | 6 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| c0004 | 0/0 | 2892 | 4 | 4 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| c0005 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| c0006 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| c0007 | 0/0 | 2892 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| c0008 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| c0009 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| c0010 | 0/0 | 2892 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| 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 | 255 | 360 | 81 | 62 | 167 | 16 | 32 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| t0002 | 0/0 | 255 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| t0003 | 0/0 | 255 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| 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 | 2892 | 270 | 50 | 49 | 136 | 12 | 21 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0002 | 0/0 | 2892 | 74 | 16 | 12 | 32 | 4 | 10 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0004 | 0/0 | 2892 | 4 | 4 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0006 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0008 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0002c0003 | 0/0 | 2892 | 6 | 6 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0003c0005 | 0/0 | 2892 | 2 | 2 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0004c0010 | 0/0 | 2892 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0005c0007 | 0/0 | 2892 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0006c0009 | 0/0 | 2892 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3146 | 268 | 49 | 49 | 135 | 12 | 21 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0001t0002 | 0/0 | 3146 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0001t0003 | 0/0 | 3146 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0002t0001 | 0/0 | 3146 | 74 | 16 | 12 | 32 | 4 | 10 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0004t0001 | 0/0 | 3146 | 4 | 4 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0006t0001 | 0/0 | 3146 | 2 | 2 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0001c0008t0001 | 0/0 | 3146 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0002c0003t0001 | 0/0 | 3146 | 6 | 6 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0003c0005t0001 | 0/0 | 3146 | 2 | 2 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0004c0010t0001 | 0/0 | 3146 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0005c0007t0001 | 0/0 | 3146 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| a0006c0009t0001 | 0/0 | 3146 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | copy fasta | chr11 | 77873720 | 77999668 |
| 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 | 2 | 0 | 1 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0016 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0006t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0001c0008t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0002c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0002c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0002c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0002c0003t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0002c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0002c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0003c0005t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0003c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0004c0010t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0005c0007t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| a0006c0009t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0121 | EUR | GBR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0094 | EUR | GBR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0355 | EUR | FIN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | FIN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | FIN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | CHS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01168 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01243 | hp2 | a0005 | c0007 | t0001 | g0079 | AMR | PUR | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0152 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0131 | EUR | IBS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0146 | EUR | IBS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | CDX | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0357 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0293 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0254 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02602 | hp2 | a0004 | c0010 | t0001 | g0109 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0292 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0114 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02647 | hp2 | a0006 | c0009 | t0001 | g0250 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0295 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02895 | hp2 | a0001 | c0006 | t0001 | g0273 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02897 | hp2 | a0001 | c0006 | t0001 | g0274 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0269 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0117 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03041 | hp1 | a0001 | c0004 | t0001 | g0255 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03130 | hp2 | a0001 | c0004 | t0001 | g0252 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03139 | hp2 | a0003 | c0005 | t0001 | g0100 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0253 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03195 | hp2 | a0002 | c0003 | t0001 | g0174 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0115 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0116 | AFR | ESN | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | GWD | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0092 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | STU | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0143 | SAS | BEB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | CHB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | CHB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | LWK | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0356 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | YRI | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ASW | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ASW | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0119 | SAS | GIH | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | GIH | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | CLM | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02559 | hp1 | a0003 | c0005 | t0001 | g0099 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0102 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | MSL | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG06807 | hp1 | a0002 | c0003 | t0001 | g0294 | AFR | USA | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | USA | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA20300 | hp1 | a0001 | c0008 | t0001 | g0156 | AFR | USA | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0213 | AFR | USA | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0016 | REF | REF | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0029 | REF | REF | INTS4_chr11_77873720_77999668 | INTS4 | chr11 | 77873720 | 77999668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77918851
|
C | T | 1 | a0005 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1892G>A | p.Gly631Glu | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/23 | 1917/3146 | 1892/2892 | 631/963 | chr11 | 77918851 | ||
| chr11:77956042
|
G | C | 1 | a0003 | 2 | HG02559.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.818C>G | p.Ser273Cys | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/23 | 843/3146 | 818/2892 | 273/963 | chr11 | 77956042 | ||
| chr11:77958806
|
T | C | 1 | a0006 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.737A>G | p.Glu246Gly | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/23 | 762/3146 | 737/2892 | 246/963 | chr11 | 77958806 | ||
| chr11:77979042
|
G | A | 1 | a0004 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.425C>T | p.Pro142Leu | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/23 | 450/3146 | 425/2892 | 142/963 | chr11 | 77979042 | ||
| chr11:77979073
|
C | T | 1 | a0002 | 6 | HG02451.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
missense_variant | MODERATE | c.394G>A | p.Asp132Asn | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/23 | 419/3146 | 394/2892 | 132/963 | chr11 | 77979073 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77924809
|
T | C | 1 | a0001c0004 | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
synonymous_variant | LOW | c.1455A>G | p.Ala485Ala | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/23 | 1480/3146 | 1455/2892 | 485/963 | chr11 | 77924809 | ||
| chr11:77924836
|
A | C | 3 | a0001c0002a0004c0010a0006c0009 | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
synonymous_variant | LOW | c.1428T>G | p.Val476Val | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/23 | 1453/3146 | 1428/2892 | 476/963 | chr11 | 77924836 | ||
| chr11:77928420
|
A | G | 3 | a0001c0002a0004c0010a0006c0009 | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
synonymous_variant | LOW | c.1293T>C | p.Ser431Ser | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/23 | 1318/3146 | 1293/2892 | 431/963 | chr11 | 77928420 | ||
| chr11:77928465
|
T | A | 3 | a0001c0002a0004c0010a0006c0009 | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
synonymous_variant | LOW | c.1248A>T | p.Leu416Leu | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/23 | 1273/3146 | 1248/2892 | 416/963 | chr11 | 77928465 | ||
| chr11:77938721
|
G | A | 1 | a0001c0008 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.1095C>T | p.Thr365Thr | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/23 | 1120/3146 | 1095/2892 | 365/963 | chr11 | 77938721 | ||
| chr11:77991267
|
T | C | 1 | a0001c0006 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.87A>G | p.Arg29Arg | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/23 | 112/3146 | 87/2892 | 29/963 | chr11 | 77991267 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77878851
|
A | G | 1 | a0001c0001t0002 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 23/23 | 98 | chr11 | 77878851 | |||||
| chr11:77878865
|
T | C | 1 | a0001c0001t0003 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*84A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 23/23 | 84 | chr11 | 77878865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:77879170
|
C | G | 1 | a0001c0001t0001g0241 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2714-43G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77879170 | ||||||
| chr11:77879279
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2714-152T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77879279 | ||||||
| chr11:77879402
|
A | C | 1 | a0001c0001t0001g0199 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2714-275T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77879402 | ||||||
| chr11:77879613
|
G | C | 1 | a0001c0001t0001g0257 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2714-486C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77879613 | ||||||
| chr11:77880371
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0265others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2714-1244C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77880371 | ||||||
| chr11:77880642
|
T | C | 1 | a0001c0002t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2714-1515A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77880642 | ||||||
| chr11:77880726
|
G | C | 1 | a0001c0001t0001g0275 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2714-1599C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77880726 | ||||||
| chr11:77880924
|
A | AAAAC | 4 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(1): Show | 4 | HG00673.hp2 HG02015.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2714-1801_2714-179 others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77880924 | ||||||
| chr11:77881098
|
CAAG | C | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2714-1974_2714-197 others(7): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881098 | ||||||
| chr11:77881150
|
A | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(140): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.2714-2023T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881150 | ||||||
| chr11:77881307
|
G | A | 6 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0265others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2714-2180C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881307 | ||||||
| chr11:77881388
|
G | C | 1 | a0002c0003t0001g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2714-2261C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881388 | ||||||
| chr11:77881476
|
A | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0022others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2714-2349T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881476 | ||||||
| chr11:77881517
|
A | G | 1 | a0001c0002t0001g0004 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2713+2315T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881517 | ||||||
| chr11:77881702
|
C | T | 1 | a0001c0001t0001g0359 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2713+2130G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881702 | ||||||
| chr11:77881863
|
G | A | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0221others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2713+1969C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881863 | ||||||
| chr11:77881899
|
T | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(62): Show | 65 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2713+1933A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881899 | ||||||
| chr11:77881911
|
G | GT | 9 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0181others(6): Show | 9 | HG00741.hp2 HG01243.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2713+1920dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881911 | ||||||
| chr11:77881990
|
C | A | 1 | a0001c0001t0001g0319 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2713+1842G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77881990 | ||||||
| chr11:77882004
|
C | G | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2713+1828G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882004 | ||||||
| chr11:77882043
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2713+1789G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882043 | ||||||
| chr11:77882070
|
C | A | 1 | a0001c0002t0001g0108 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2713+1762G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882070 | ||||||
| chr11:77882094
|
A | G | 1 | a0001c0001t0001g0337 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2713+1738T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882094 | ||||||
| chr11:77882175
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(59): Show | 62 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2713+1657G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882175 | ||||||
| chr11:77882200
|
G | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2713+1632C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882200 | ||||||
| chr11:77882301
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(62): Show | 65 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.2713+1531T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882301 | ||||||
| chr11:77882401
|
G | GT | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.2713+1430_2713+143 others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882401 | ||||||
| chr11:77882475
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2713+1357G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882475 | ||||||
| chr11:77882647
|
G | C | 2 | a0003c0005t0001g0099a0003c0005t0001g0100 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2713+1185C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882647 | ||||||
| chr11:77882797
|
G | A | 4 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.2713+1035C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882797 | ||||||
| chr11:77882820
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2713+1012G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77882820 | ||||||
| chr11:77883029
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2713+803A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883029 | ||||||
| chr11:77883069
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2713+763C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883069 | ||||||
| chr11:77883075
|
A | AAAT | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.2713+754_2713+756d others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883075 | ||||||
| chr11:77883075
|
A | AAATAAT | 10 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0200others(7): Show | 10 | HG00639.hp2 HG01243.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.2713+751_2713+756d others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883075 | ||||||
| chr11:77883075
|
A | AAATAATA others(5): Show |
2 | a0001c0001t0001g0098a0001c0001t0001g0266 | 2 | HG01074.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2713+745_2713+756d others(14): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883075 | ||||||
| chr11:77883075
|
A | AAATAATA others(11): Show |
1 | a0002c0003t0001g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2713+739_2713+756d others(20): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883075 | ||||||
| chr11:77883133
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0189 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2713+699C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883133 | ||||||
| chr11:77883154
|
T | A | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2713+678A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883154 | ||||||
| chr11:77883308
|
A | G | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0221others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2713+524T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883308 | ||||||
| chr11:77883333
|
A | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0189 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2713+499T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883333 | ||||||
| chr11:77883409
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0299 | 3 | HG01243.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2713+423A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 22/22 | chr11 | 77883409 | ||||||
| chr11:77884014
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2593-62T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77884014 | ||||||
| chr11:77884016
|
G | C | 1 | a0001c0001t0001g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2593-64C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77884016 | ||||||
| chr11:77884034
|
C | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(43): Show | 46 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.2593-82G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77884034 | ||||||
| chr11:77884136
|
T | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0196others(1): Show | 4 | HG02132.hp2 NA18968.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2593-184A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77884136 | ||||||
| chr11:77884596
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2593-644T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77884596 | ||||||
| chr11:77884671
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2593-719G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77884671 | ||||||
| chr11:77884852
|
G | A | 1 | a0002c0003t0001g0213 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2593-900C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77884852 | ||||||
| chr11:77884901
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0062 | 2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.2593-949G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77884901 | ||||||
| chr11:77884911
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0266a0002c0003t0001g0292 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2593-959G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77884911 | ||||||
| chr11:77885056
|
A | G | 1 | a0001c0001t0001g0337 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2593-1104T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77885056 | ||||||
| chr11:77885058
|
C | A | 43 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0221others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.2593-1106G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77885058 | ||||||
| chr11:77885230
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2593-1278C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77885230 | ||||||
| chr11:77885595
|
G | C | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2593-1643C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77885595 | ||||||
| chr11:77885696
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0266a0002c0003t0001g0292 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2593-1744C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77885696 | ||||||
| chr11:77885727
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2593-1775C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77885727 | ||||||
| chr11:77885964
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2593-2012C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77885964 | ||||||
| chr11:77886053
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(61): Show | 64 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.2593-2101T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886053 | ||||||
| chr11:77886251
|
T | C | 1 | a0001c0002t0001g0154 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2593-2299A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886251 | ||||||
| chr11:77886297
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2593-2345G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886297 | ||||||
| chr11:77886440
|
C | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.2593-2488G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886440 | ||||||
| chr11:77886442
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2593-2490G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886442 | ||||||
| chr11:77886475
|
G | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0265others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2593-2523C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886475 | ||||||
| chr11:77886521
|
C | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(143): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.2593-2569G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886521 | ||||||
| chr11:77886586
|
T | C | 1 | a0001c0001t0001g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2593-2634A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886586 | ||||||
| chr11:77886748
|
G | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.2593-2796C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886748 | ||||||
| chr11:77886751
|
C | G | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2593-2799G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886751 | ||||||
| chr11:77886759
|
G | A | 1 | a0001c0002t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2593-2807C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886759 | ||||||
| chr11:77886762
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0266a0002c0003t0001g0292 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2593-2810G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886762 | ||||||
| chr11:77886787
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02615.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2593-2835T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886787 | ||||||
| chr11:77886793
|
C | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.2593-2841G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886793 | ||||||
| chr11:77886824
|
T | C | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0221others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2593-2872A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886824 | ||||||
| chr11:77886861
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2593-2909G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77886861 | ||||||
| chr11:77887024
|
TC | T | 3 | a0001c0002t0001g0302a0001c0002t0001g0303a0001c0002t0001g0304 | 3 | NA18973.hp1 NA19055.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2593-3073delG | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887024 | ||||||
| chr11:77887166
|
A | C | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2593-3214T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887166 | ||||||
| chr11:77887257
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0214 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2593-3305C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887257 | ||||||
| chr11:77887260
|
G | A | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0221others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2593-3308C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887260 | ||||||
| chr11:77887262
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2593-3310A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887262 | ||||||
| chr11:77887294
|
T | G | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0221others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2593-3342A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887294 | ||||||
| chr11:77887415
|
C | T | 1 | a0001c0004t0001g0254 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2593-3463G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887415 | ||||||
| chr11:77887484
|
T | C | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0221others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2593-3532A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887484 | ||||||
| chr11:77887534
|
G | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.2593-3582C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887534 | ||||||
| chr11:77887553
|
T | C | 3 | a0001c0001t0001g0337a0001c0001t0001g0340a0001c0001t0001g0358 | 3 | NA18970.hp2 NA19075.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2593-3601A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887553 | ||||||
| chr11:77887717
|
A | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(63): Show | 66 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.2592+3602T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887717 | ||||||
| chr11:77887720
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2592+3599T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887720 | ||||||
| chr11:77887771
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0221others(1): Show | 4 | HG01928.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.2592+3548C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887771 | ||||||
| chr11:77887932
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2592+3387T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77887932 | ||||||
| chr11:77888110
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(132): Show | 136 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.2592+3209G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888110 | ||||||
| chr11:77888154
|
T | C | 3 | a0001c0002t0001g0114a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02647.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2592+3165A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888154 | ||||||
| chr11:77888212
|
T | G | 20 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(17): Show | 20 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.2592+3107A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888212 | ||||||
| chr11:77888238
|
G | A | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2592+3081C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888238 | ||||||
| chr11:77888268
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0265others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2592+3051G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888268 | ||||||
| chr11:77888314
|
G | A | 2 | a0001c0002t0001g0104a0001c0002t0001g0105 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2592+3005C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888314 | ||||||
| chr11:77888504
|
A | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(138): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.2592+2815T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888504 | ||||||
| chr11:77888530
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.2592+2789A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888530 | ||||||
| chr11:77888562
|
A | G | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2592+2757T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888562 | ||||||
| chr11:77888576
|
G | C | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2592+2743C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888576 | ||||||
| chr11:77888602
|
C | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0265others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2592+2717G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888602 | ||||||
| chr11:77888617
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(73): Show | 76 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.2592+2702A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888617 | ||||||
| chr11:77888640
|
A | C | 3 | a0001c0001t0001g0098a0001c0001t0001g0266a0002c0003t0001g0292 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2592+2679T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888640 | ||||||
| chr11:77888663
|
G | A | 2 | a0001c0001t0001g0098a0002c0003t0001g0292 | 2 | HG01074.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2592+2656C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888663 | ||||||
| chr11:77888664
|
T | C | 3 | a0001c0001t0001g0098a0001c0001t0001g0266a0002c0003t0001g0292 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2592+2655A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888664 | ||||||
| chr11:77888870
|
G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(141): Show | 144 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.2592+2449C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77888870 | ||||||
| chr11:77889014
|
T | G | 68 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0221others(65): Show | 68 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2592+2305A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889014 | ||||||
| chr11:77889038
|
C | T | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2592+2281G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889038 | ||||||
| chr11:77889088
|
G | A | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2592+2231C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889088 | ||||||
| chr11:77889102
|
G | T | 1 | a0006c0009t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2592+2217C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889102 | ||||||
| chr11:77889135
|
T | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0265others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2592+2184A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889135 | ||||||
| chr11:77889315
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0036others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.2592+2004T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889315 | ||||||
| chr11:77889453
|
G | A | 3 | a0001c0001t0001g0098a0001c0001t0001g0266a0002c0003t0001g0292 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2592+1866C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889453 | ||||||
| chr11:77889472
|
A | G | 3 | a0001c0004t0001g0253a0001c0004t0001g0254a0001c0004t0001g0255 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2592+1847T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889472 | ||||||
| chr11:77889494
|
G | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0266a0002c0003t0001g0292 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2592+1825C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889494 | ||||||
| chr11:77889681
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2592+1638C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889681 | ||||||
| chr11:77889682
|
A | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2592+1637T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889682 | ||||||
| chr11:77889917
|
G | C | 3 | a0001c0002t0001g0114a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02647.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2592+1402C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77889917 | ||||||
| chr11:77890223
|
G | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2592+1096C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77890223 | ||||||
| chr11:77890271
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0299 | 3 | HG01243.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2592+1048G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77890271 | ||||||
| chr11:77890525
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2592+794C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77890525 | ||||||
| chr11:77890544
|
G | T | 1 | a0001c0001t0001g0337 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2592+775C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77890544 | ||||||
| chr11:77890739
|
G | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2592+580C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77890739 | ||||||
| chr11:77890807
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0193 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2592+512A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77890807 | ||||||
| chr11:77891043
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2592+276G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77891043 | ||||||
| chr11:77891271
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2592+48T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 21/22 | chr11 | 77891271 | ||||||
| chr11:77891627
|
A | G | 64 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2448+54T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 20/22 | chr11 | 77891627 | ||||||
| chr11:77892026
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2289-186G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892026 | ||||||
| chr11:77892184
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2289-344C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892184 | ||||||
| chr11:77892215
|
G | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(60): Show | 63 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2289-375C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892215 | ||||||
| chr11:77892235
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0181a0001c0001t0001g0299others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2289-395G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892235 | ||||||
| chr11:77892387
|
T | C | 3 | a0001c0001t0001g0098a0001c0001t0001g0266a0002c0003t0001g0292 | 3 | HG01074.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2289-547A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892387 | ||||||
| chr11:77892474
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(63): Show | 66 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.2289-634A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892474 | ||||||
| chr11:77892614
|
G | A | 4 | a0001c0002t0001g0128a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2289-774C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892614 | ||||||
| chr11:77892708
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.2289-868C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892708 | ||||||
| chr11:77892834
|
C | T | 22 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(19): Show | 22 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.2289-994G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892834 | ||||||
| chr11:77892835
|
A | G | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.2289-995T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892835 | ||||||
| chr11:77892876
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 132 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.2289-1036G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77892876 | ||||||
| chr11:77893025
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(60): Show | 63 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2289-1185C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893025 | ||||||
| chr11:77893123
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2288+1167C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893123 | ||||||
| chr11:77893154
|
G | A | 1 | a0001c0002t0001g0267 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2288+1136C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893154 | ||||||
| chr11:77893240
|
T | G | 1 | a0001c0001t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2288+1050A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893240 | ||||||
| chr11:77893448
|
AT | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2288+841delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893448 | ||||||
| chr11:77893450
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(60): Show | 63 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2288+840T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893450 | ||||||
| chr11:77893618
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2288+672C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893618 | ||||||
| chr11:77893672
|
C | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0239 | 2 | NA18977.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2288+618G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893672 | ||||||
| chr11:77893891
|
T | TTAAA | 3 | a0001c0001t0001g0008a0001c0001t0001g0198a0001c0001t0001g0205 | 3 | HG00140.hp2 HG01346.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2288+395_2288+398d others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893891 | ||||||
| chr11:77893891
|
T | TTAAATAA others(1): Show |
221 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(218): Show | 222 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.2288+391_2288+398d others(10): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893891 | ||||||
| chr11:77893891
|
T | TTAAATAA others(5): Show |
97 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(94): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.2288+387_2288+398d others(14): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893891 | ||||||
| chr11:77893891
|
T | TTAAATAA others(9): Show |
28 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0030others(25): Show | 28 | HG01168.hp1 HG01243.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.2288+383_2288+398d others(18): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893891 | ||||||
| chr11:77893891
|
T | TTAAATAA others(13): Show |
4 | a0001c0001t0001g0199a0001c0001t0001g0286a0001c0002t0001g0092others(1): Show | 4 | HG01070.hp1 HG03098.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.2288+379_2288+398d others(22): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893891 | ||||||
| chr11:77893891
|
TTAAA | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2288+395_2288+398d others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893891 | ||||||
| chr11:77893940
|
G | C | 1 | a0001c0001t0001g0028 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2288+350C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893940 | ||||||
| chr11:77893994
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2288+296G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77893994 | ||||||
| chr11:77894232
|
A | C | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2288+58T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 19/22 | chr11 | 77894232 | ||||||
| chr11:77894455
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.2229-106A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77894455 | ||||||
| chr11:77895123
|
C | CT | 50 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(47): Show | 50 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2229-775dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895123 | ||||||
| chr11:77895171
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2229-822C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895171 | ||||||
| chr11:77895527
|
G | GA | 8 | a0001c0001t0001g0081a0001c0002t0001g0116a0001c0002t0001g0121others(5): Show | 8 | HG00099.hp2 HG01516.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.2229-1179dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895527 | ||||||
| chr11:77895527
|
GA | G | 75 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0027others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.2229-1179delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895527 | ||||||
| chr11:77895527
|
GAA | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0019others(53): Show | 56 | HG00323.hp1 HG01074.hp2 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.2229-1180_2229-117 others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895527 | ||||||
| chr11:77895527
|
GAAA | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.2229-1181_2229-117 others(7): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895527 | ||||||
| chr11:77895527
|
GAAAA | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0162others(5): Show | 8 | HG02523.hp1 HG02723.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.2229-1182_2229-117 others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895527 | ||||||
| chr11:77895527
|
GAAAAAAA others(3): Show |
G | 20 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(17): Show | 20 | HG00639.hp2 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.2229-1188_2229-117 others(14): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895527 | ||||||
| chr11:77895527
|
GAAAAAAA others(5): Show |
G | 1 | a0001c0001t0001g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2229-1190_2229-117 others(16): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895527 | ||||||
| chr11:77895527
|
GAAAAAAA others(6): Show |
G | 2 | a0001c0001t0001g0098a0002c0003t0001g0292 | 2 | HG01074.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2229-1191_2229-117 others(17): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895527 | ||||||
| chr11:77895530
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0216 | 2 | NA18947.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2229-1181T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895530 | ||||||
| chr11:77895531
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2229-1182T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895531 | ||||||
| chr11:77895982
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2229-1633A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77895982 | ||||||
| chr11:77896296
|
G | A | 1 | a0001c0001t0001g0312 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2229-1947C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896296 | ||||||
| chr11:77896299
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2229-1950A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896299 | ||||||
| chr11:77896391
|
C | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2229-2042G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896391 | ||||||
| chr11:77896435
|
G | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2229-2086C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896435 | ||||||
| chr11:77896509
|
G | A | 1 | a0001c0002t0001g0092 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2229-2160C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896509 | ||||||
| chr11:77896523
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2229-2174T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896523 | ||||||
| chr11:77896543
|
T | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.2229-2194A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896543 | ||||||
| chr11:77896604
|
T | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.2229-2255A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896604 | ||||||
| chr11:77896652
|
C | CA | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(3): Show | 6 | HG02615.hp1 HG02630.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2229-2304dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896652 | ||||||
| chr11:77896652
|
CAA | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(75): Show | 78 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.2229-2305_2229-230 others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896652 | ||||||
| chr11:77896829
|
C | T | 2 | a0001c0002t0001g0101a0001c0002t0001g0102 | 2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2229-2480G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896829 | ||||||
| chr11:77896910
|
G | T | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2229-2561C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896910 | ||||||
| chr11:77896911
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2229-2562T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896911 | ||||||
| chr11:77896912
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2229-2563T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896912 | ||||||
| chr11:77896913
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2229-2564T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896913 | ||||||
| chr11:77896921
|
CAGAAAGA others(703): Show |
C | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2229-3282_2229-257 others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77896921 | ||||||
| chr11:77897055
|
A | G | 62 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(59): Show | 62 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2229-2706T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897055 | ||||||
| chr11:77897060
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.2229-2711C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897060 | ||||||
| chr11:77897364
|
A | T | 1 | a0001c0002t0001g0117 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2229-3015T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897364 | ||||||
| chr11:77897381
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2229-3032T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897381 | ||||||
| chr11:77897447
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2229-3098A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897447 | ||||||
| chr11:77897508
|
A | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(60): Show | 63 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.2229-3159T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897508 | ||||||
| chr11:77897523
|
C | T | 3 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0001g0359 | 3 | NA18965.hp2 NA18967.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2229-3174G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897523 | ||||||
| chr11:77897542
|
C | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0299others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2229-3193G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897542 | ||||||
| chr11:77897561
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2229-3212A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897561 | ||||||
| chr11:77897625
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2229-3276G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897625 | ||||||
| chr11:77897634
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2229-3285C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897634 | ||||||
| chr11:77897650
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2229-3301C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897650 | ||||||
| chr11:77897667
|
A | AT | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(137): Show | 141 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.2229-3319dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897667 | ||||||
| chr11:77897675
|
T | A | 1 | a0001c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2229-3326A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897675 | ||||||
| chr11:77897724
|
C | A | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2229-3375G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897724 | ||||||
| chr11:77897741
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2229-3392C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77897741 | ||||||
| chr11:77898103
|
A | C | 1 | a0001c0001t0001g0243 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2228+3318T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77898103 | ||||||
| chr11:77898437
|
C | T | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2228+2984G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77898437 | ||||||
| chr11:77898827
|
A | T | 1 | a0001c0001t0001g0165 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2228+2594T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77898827 | ||||||
| chr11:77899167
|
G | A | 3 | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0336 | 3 | HG00408.hp2 HG02523.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.2228+2254C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899167 | ||||||
| chr11:77899174
|
G | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(59): Show | 62 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.2228+2247C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899174 | ||||||
| chr11:77899192
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2228+2229A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899192 | ||||||
| chr11:77899243
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2228+2178G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899243 | ||||||
| chr11:77899284
|
AG | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.2228+2136delC | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899284 | ||||||
| chr11:77899500
|
G | A | 5 | a0002c0003t0001g0174a0002c0003t0001g0213a0002c0003t0001g0293others(2): Show | 5 | HG02451.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2228+1921C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899500 | ||||||
| chr11:77899651
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2228+1770G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899651 | ||||||
| chr11:77899776
|
C | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.2228+1645G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899776 | ||||||
| chr11:77899788
|
T | C | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0021others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.2228+1633A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899788 | ||||||
| chr11:77899984
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0116 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2228+1437G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77899984 | ||||||
| chr11:77900100
|
C | CT | 81 | a0001c0001t0001g0015a0001c0001t0001g0021a0001c0001t0001g0022others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.2228+1320dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900100 | ||||||
| chr11:77900117
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2228+1304T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900117 | ||||||
| chr11:77900168
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0319 | 2 | HG00544.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.2228+1253G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900168 | ||||||
| chr11:77900247
|
A | C | 1 | a0001c0001t0001g0260 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2228+1174T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900247 | ||||||
| chr11:77900248
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2228+1173A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900248 | ||||||
| chr11:77900256
|
T | C | 1 | a0001c0001t0001g0011 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2228+1165A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900256 | ||||||
| chr11:77900271
|
A | T | 2 | a0001c0002t0001g0268a0001c0002t0001g0269 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2228+1150T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900271 | ||||||
| chr11:77900290
|
A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0299 | 3 | HG01243.hp1 HG03942.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2228+1131T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900290 | ||||||
| chr11:77900301
|
A | G | 2 | a0001c0002t0001g0129a0001c0002t0001g0150 | 2 | HG01358.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2228+1120T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900301 | ||||||
| chr11:77900353
|
C | A | 1 | a0001c0001t0001g0331 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2228+1068G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900353 | ||||||
| chr11:77900376
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2228+1045C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900376 | ||||||
| chr11:77900385
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2228+1036G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900385 | ||||||
| chr11:77900389
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2228+1032T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900389 | ||||||
| chr11:77900391
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2228+1030T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900391 | ||||||
| chr11:77900488
|
G | A | 3 | a0001c0002t0001g0114a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02647.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2228+933C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900488 | ||||||
| chr11:77900686
|
G | A | 10 | a0001c0002t0001g0118a0001c0002t0001g0122a0001c0002t0001g0135others(7): Show | 10 | HG00408.hp1 HG00609.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.2228+735C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900686 | ||||||
| chr11:77900909
|
G | A | 1 | a0001c0002t0001g0118 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2228+512C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77900909 | ||||||
| chr11:77901218
|
G | C | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2228+203C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 18/22 | chr11 | 77901218 | ||||||
| chr11:77901555
|
T | G | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
splice_region_variant&intron_variant | LOW | c.2098-4A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77901555 | ||||||
| chr11:77901738
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(204): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.2098-187G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77901738 | ||||||
| chr11:77901870
|
T | A | 4 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0278others(1): Show | 4 | HG02071.hp1 NA18939.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.2098-319A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77901870 | ||||||
| chr11:77901893
|
T | G | 1 | a0001c0001t0001g0159 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2098-342A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77901893 | ||||||
| chr11:77902012
|
A | T | 1 | a0001c0002t0001g0119 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2098-461T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77902012 | ||||||
| chr11:77902025
|
A | G | 5 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0330others(2): Show | 5 | HG00408.hp2 HG00544.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.2098-474T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77902025 | ||||||
| chr11:77902154
|
G | A | 14 | a0001c0001t0001g0037a0001c0001t0001g0050a0001c0001t0001g0051others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2098-603C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77902154 | ||||||
| chr11:77902392
|
G | A | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2098-841C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77902392 | ||||||
| chr11:77902693
|
C | G | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2097+847G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77902693 | ||||||
| chr11:77902871
|
G | A | 1 | a0001c0002t0001g0152 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2097+669C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77902871 | ||||||
| chr11:77902906
|
C | A | 1 | a0001c0001t0001g0337 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2097+634G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77902906 | ||||||
| chr11:77902971
|
T | C | 2 | a0001c0002t0001g0268a0001c0002t0001g0269 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2097+569A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77902971 | ||||||
| chr11:77902993
|
C | T | 1 | a0001c0002t0001g0092 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2097+547G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77902993 | ||||||
| chr11:77903000
|
C | A | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2097+540G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77903000 | ||||||
| chr11:77903065
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0297 | 2 | HG01175.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2097+475G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77903065 | ||||||
| chr11:77903109
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2097+431A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77903109 | ||||||
| chr11:77903162
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2097+378C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77903162 | ||||||
| chr11:77903172
|
C | T | 20 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(17): Show | 20 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.2097+368G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77903172 | ||||||
| chr11:77903249
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2097+291A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77903249 | ||||||
| chr11:77903420
|
G | GCCACAAC others(172): Show |
1 | a0001c0002t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2038_2097+119dupAA others(177): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 17/22 | chr11 | 77903420 | ||||||
| chr11:77903724
|
T | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 128 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.2017-104A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77903724 | ||||||
| chr11:77903929
|
C | T | 2 | a0001c0002t0001g0106a0001c0002t0001g0108 | 2 | NA18963.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.2017-309G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77903929 | ||||||
| chr11:77903930
|
G | A | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-310C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77903930 | ||||||
| chr11:77904160
|
C | A | 1 | a0001c0002t0001g0256 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2017-540G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77904160 | ||||||
| chr11:77904204
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2017-584T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77904204 | ||||||
| chr11:77904302
|
T | C | 2 | a0001c0002t0001g0281a0001c0002t0001g0291 | 2 | NA18961.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2017-682A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77904302 | ||||||
| chr11:77904336
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2017-716G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77904336 | ||||||
| chr11:77904382
|
T | C | 50 | a0001c0001t0001g0023a0001c0002t0001g0004a0001c0002t0001g0005others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.2017-762A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77904382 | ||||||
| chr11:77904386
|
A | C | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2017-766T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77904386 | ||||||
| chr11:77904567
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.2017-947A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77904567 | ||||||
| chr11:77905094
|
G | A | 6 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2017-1474C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905094 | ||||||
| chr11:77905119
|
C | T | 1 | a0001c0004t0001g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2017-1499G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905119 | ||||||
| chr11:77905222
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.2017-1602G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905222 | ||||||
| chr11:77905409
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2017-1789C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905409 | ||||||
| chr11:77905456
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2017-1836G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905456 | ||||||
| chr11:77905458
|
C | CA | 10 | a0001c0001t0001g0003a0001c0001t0001g0251a0001c0001t0001g0286others(7): Show | 10 | HG01243.hp1 HG02300.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.2017-1839dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905458 | ||||||
| chr11:77905532
|
C | T | 70 | a0001c0001t0001g0023a0001c0002t0001g0004a0001c0002t0001g0005others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.2017-1912G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905532 | ||||||
| chr11:77905574
|
T | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2017-1954A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905574 | ||||||
| chr11:77905606
|
C | T | 2 | a0001c0002t0001g0112a0001c0002t0001g0113 | 2 | HG01496.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2017-1986G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905606 | ||||||
| chr11:77905729
|
A | G | 6 | a0002c0003t0001g0174a0002c0003t0001g0213a0002c0003t0001g0292others(3): Show | 6 | HG02451.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2016+1988T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905729 | ||||||
| chr11:77905752
|
A | G | 4 | a0001c0002t0001g0300a0001c0002t0001g0302a0001c0002t0001g0303others(1): Show | 4 | NA18973.hp1 NA18994.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.2016+1965T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905752 | ||||||
| chr11:77905903
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2016+1814G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77905903 | ||||||
| chr11:77906040
|
T | A | 5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(2): Show | 5 | HG00738.hp2 HG01167.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.2016+1677A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906040 | ||||||
| chr11:77906100
|
TGGGATTT others(9): Show |
T | 10 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108others(7): Show | 10 | HG02602.hp2 HG03654.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.2016+1601_2016+161 others(20): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906100 | ||||||
| chr11:77906118
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0066 | 2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.2016+1599C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906118 | ||||||
| chr11:77906163
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2016+1554G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906163 | ||||||
| chr11:77906347
|
G | C | 1 | a0001c0001t0001g0006 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2016+1370C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906347 | ||||||
| chr11:77906387
|
G | A | 70 | a0001c0001t0001g0023a0001c0002t0001g0004a0001c0002t0001g0005others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.2016+1330C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906387 | ||||||
| chr11:77906391
|
T | C | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2016+1326A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906391 | ||||||
| chr11:77906587
|
A | T | 2 | a0003c0005t0001g0099a0003c0005t0001g0100 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2016+1130T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906587 | ||||||
| chr11:77906677
|
G | A | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.2016+1040C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906677 | ||||||
| chr11:77906904
|
A | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 127 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.2016+813T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77906904 | ||||||
| chr11:77907020
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 127 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.2016+697G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77907020 | ||||||
| chr11:77907395
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(130): Show | 134 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.2016+322C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 16/22 | chr11 | 77907395 | ||||||
| chr11:77907942
|
G | A | 20 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(17): Show | 20 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.1923-132C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77907942 | ||||||
| chr11:77907963
|
T | G | 1 | a0001c0002t0001g0131 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1923-153A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77907963 | ||||||
| chr11:77907980
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0299others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1923-170A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77907980 | ||||||
| chr11:77908056
|
G | GT | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(357): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1923-247dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908056 | ||||||
| chr11:77908084
|
T | TA | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(357): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1923-275dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908084 | ||||||
| chr11:77908293
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1923-483A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908293 | ||||||
| chr11:77908303
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1923-493G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908303 | ||||||
| chr11:77908462
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1923-652C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908462 | ||||||
| chr11:77908466
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1923-656A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908466 | ||||||
| chr11:77908617
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1923-807C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908617 | ||||||
| chr11:77908659
|
A | G | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923-849T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908659 | ||||||
| chr11:77908689
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1923-879A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908689 | ||||||
| chr11:77908816
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1923-1006A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908816 | ||||||
| chr11:77908846
|
T | TA | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1923-1037dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908846 | ||||||
| chr11:77908930
|
G | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0299others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1923-1120C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77908930 | ||||||
| chr11:77909084
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1923-1274G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909084 | ||||||
| chr11:77909099
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1923-1289G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909099 | ||||||
| chr11:77909174
|
A | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0061 | 2 | HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1923-1364T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909174 | ||||||
| chr11:77909294
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1923-1484A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909294 | ||||||
| chr11:77909458
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1923-1648A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909458 | ||||||
| chr11:77909489
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0080 | 2 | HG02083.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1923-1679C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909489 | ||||||
| chr11:77909710
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1923-1900G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909710 | ||||||
| chr11:77909848
|
A | G | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923-2038T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909848 | ||||||
| chr11:77909855
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1923-2045G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909855 | ||||||
| chr11:77909955
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1923-2145C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909955 | ||||||
| chr11:77909961
|
G | A | 1 | a0001c0002t0001g0131 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1923-2151C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77909961 | ||||||
| chr11:77910034
|
G | C | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1923-2224C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910034 | ||||||
| chr11:77910035
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1923-2225G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910035 | ||||||
| chr11:77910036
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1923-2226T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910036 | ||||||
| chr11:77910271
|
T | G | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0202others(1): Show | 4 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923-2461A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910271 | ||||||
| chr11:77910320
|
G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(198): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1923-2510C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910320 | ||||||
| chr11:77910385
|
T | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1923-2575A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910385 | ||||||
| chr11:77910463
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1923-2653C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910463 | ||||||
| chr11:77910497
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1923-2687C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910497 | ||||||
| chr11:77910498
|
T | C | 2 | a0001c0001t0001g0318a0001c0001t0001g0324 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1923-2688A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910498 | ||||||
| chr11:77910509
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0214 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1923-2699C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910509 | ||||||
| chr11:77910522
|
A | G | 2 | a0001c0001t0001g0318a0001c0001t0001g0324 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1923-2712T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910522 | ||||||
| chr11:77910714
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1923-2904C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910714 | ||||||
| chr11:77910724
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1923-2914A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910724 | ||||||
| chr11:77910853
|
A | G | 1 | a0001c0001t0001g0041 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1923-3043T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910853 | ||||||
| chr11:77910865
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1923-3055C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910865 | ||||||
| chr11:77910867
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1923-3057C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77910867 | ||||||
| chr11:77911228
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1923-3418C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77911228 | ||||||
| chr11:77911286
|
A | G | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1923-3476T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77911286 | ||||||
| chr11:77911347
|
T | C | 2 | a0001c0002t0001g0268a0001c0002t0001g0269 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1923-3537A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77911347 | ||||||
| chr11:77911487
|
T | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0072 | 2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1923-3677A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77911487 | ||||||
| chr11:77911576
|
C | A | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1923-3766G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77911576 | ||||||
| chr11:77911699
|
T | C | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923-3889A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77911699 | ||||||
| chr11:77911794
|
G | C | 2 | a0003c0005t0001g0099a0003c0005t0001g0100 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1923-3984C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77911794 | ||||||
| chr11:77912044
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1923-4234G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912044 | ||||||
| chr11:77912079
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1923-4269G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912079 | ||||||
| chr11:77912244
|
C | T | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1923-4434G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912244 | ||||||
| chr11:77912315
|
T | C | 1 | a0001c0001t0001g0320 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1923-4505A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912315 | ||||||
| chr11:77912362
|
C | CA | 16 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0157others(13): Show | 16 | HG01175.hp1 HG01361.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1923-4553dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912362 | ||||||
| chr11:77912412
|
C | T | 1 | a0001c0001t0003g0259 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1923-4602G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912412 | ||||||
| chr11:77912443
|
G | A | 7 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(4): Show | 7 | HG00735.hp1 HG01433.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.1923-4633C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912443 | ||||||
| chr11:77912466
|
A | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1923-4656T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912466 | ||||||
| chr11:77912603
|
G | T | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | NA19005.hp2 NA19068.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1923-4793C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912603 | ||||||
| chr11:77912621
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1923-4811G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912621 | ||||||
| chr11:77912697
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1923-4887A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912697 | ||||||
| chr11:77912736
|
G | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1923-4926C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912736 | ||||||
| chr11:77912775
|
C | T | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1923-4965G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912775 | ||||||
| chr11:77912827
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1923-5017A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77912827 | ||||||
| chr11:77913032
|
T | C | 2 | a0001c0002t0001g0268a0001c0002t0001g0269 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1923-5222A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77913032 | ||||||
| chr11:77913131
|
G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1923-5321C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77913131 | ||||||
| chr11:77913307
|
A | AT | 43 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0027others(40): Show | 43 | HG00735.hp1 HG01074.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.1923-5498dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77913307 | ||||||
| chr11:77913307
|
AT | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0042others(82): Show | 85 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1923-5498delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77913307 | ||||||
| chr11:77913448
|
A | G | 5 | a0001c0002t0001g0110a0001c0002t0001g0300a0001c0002t0001g0302others(2): Show | 5 | NA18959.hp2 NA18973.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1922+5373T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77913448 | ||||||
| chr11:77913457
|
A | G | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1922+5364T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77913457 | ||||||
| chr11:77913468
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922+5353G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77913468 | ||||||
| chr11:77913950
|
A | G | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922+4871T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77913950 | ||||||
| chr11:77914189
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1922+4632T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77914189 | ||||||
| chr11:77914318
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1922+4503A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77914318 | ||||||
| chr11:77914337
|
T | C | 1 | a0001c0002t0001g0138 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1922+4484A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77914337 | ||||||
| chr11:77914609
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1922+4212A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77914609 | ||||||
| chr11:77914624
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1922+4197G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77914624 | ||||||
| chr11:77914636
|
G | A | 1 | a0006c0009t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1922+4185C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77914636 | ||||||
| chr11:77914777
|
G | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0299 | 2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1922+4044C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77914777 | ||||||
| chr11:77915014
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1922+3807A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77915014 | ||||||
| chr11:77915122
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1922+3699A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77915122 | ||||||
| chr11:77915234
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(119): Show | 123 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1922+3587A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77915234 | ||||||
| chr11:77915288
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1922+3533G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77915288 | ||||||
| chr11:77915369
|
A | G | 5 | a0001c0001t0001g0317a0001c0001t0001g0319a0001c0001t0001g0330others(2): Show | 5 | HG00408.hp2 HG00544.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1922+3452T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77915369 | ||||||
| chr11:77915598
|
C | G | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0202others(1): Show | 4 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922+3223G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77915598 | ||||||
| chr11:77915861
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1922+2960C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77915861 | ||||||
| chr11:77915917
|
A | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1922+2904T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77915917 | ||||||
| chr11:77915941
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1922+2880A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77915941 | ||||||
| chr11:77916012
|
T | TCATTGTG others(3): Show |
1 | a0001c0001t0001g0157 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1922+2799_1922+280 others(14): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77916012 | ||||||
| chr11:77916179
|
G | C | 1 | a0001c0001t0001g0025 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1922+2642C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77916179 | ||||||
| chr11:77916250
|
T | C | 1 | a0001c0002t0001g0256 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1922+2571A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77916250 | ||||||
| chr11:77916360
|
C | G | 1 | a0001c0001t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1922+2461G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77916360 | ||||||
| chr11:77916385
|
G | C | 74 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1922+2436C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77916385 | ||||||
| chr11:77916619
|
G | A | 1 | a0001c0002t0001g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1922+2202C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77916619 | ||||||
| chr11:77916983
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1922+1838T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77916983 | ||||||
| chr11:77916989
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1922+1832T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77916989 | ||||||
| chr11:77916993
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1922+1828T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77916993 | ||||||
| chr11:77917062
|
T | C | 21 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.1922+1759A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917062 | ||||||
| chr11:77917091
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1922+1730G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917091 | ||||||
| chr11:77917105
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1922+1716C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917105 | ||||||
| chr11:77917219
|
T | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1922+1602A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917219 | ||||||
| chr11:77917319
|
C | CT | 75 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1922+1501dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917319 | ||||||
| chr11:77917319
|
CT | C | 8 | a0001c0001t0001g0192a0001c0002t0001g0112a0001c0002t0001g0113others(5): Show | 8 | HG00639.hp2 HG01496.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1922+1501delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917319 | ||||||
| chr11:77917327
|
T | C | 12 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0183others(9): Show | 12 | HG01123.hp1 NA18962.hp2 NA18977.hp2 others(9): Show |
intron_variant | MODIFIER | c.1922+1494A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917327 | ||||||
| chr11:77917403
|
TC | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1922+1417delG | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917403 | ||||||
| chr11:77917428
|
C | A | 1 | a0001c0001t0001g0310 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1922+1393G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917428 | ||||||
| chr11:77917557
|
G | T | 1 | a0001c0002t0001g0111 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1922+1264C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917557 | ||||||
| chr11:77917629
|
T | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0196others(1): Show | 4 | HG02132.hp2 NA18968.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922+1192A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917629 | ||||||
| chr11:77917685
|
T | G | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1922+1136A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917685 | ||||||
| chr11:77917922
|
G | A | 70 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.1922+899C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77917922 | ||||||
| chr11:77918007
|
C | T | 21 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.1922+814G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918007 | ||||||
| chr11:77918028
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1922+793A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918028 | ||||||
| chr11:77918072
|
G | C | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1922+749C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918072 | ||||||
| chr11:77918086
|
A | AT | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1922+734dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918086 | ||||||
| chr11:77918268
|
C | CA | 8 | a0001c0001t0001g0185a0001c0001t0001g0218a0001c0001t0001g0342others(5): Show | 8 | HG02071.hp2 HG02135.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1922+552dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918268 | ||||||
| chr11:77918274
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1922+547T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918274 | ||||||
| chr11:77918416
|
C | CA | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(77): Show | 81 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.1922+404dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918416 | ||||||
| chr11:77918416
|
C | CAA | 46 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0019others(43): Show | 46 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1922+403_1922+404d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918416 | ||||||
| chr11:77918416
|
C | CAAA | 9 | a0001c0001t0001g0020a0001c0001t0001g0165a0001c0001t0001g0178others(6): Show | 9 | HG00544.hp1 HG02056.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.1922+402_1922+404d others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918416 | ||||||
| chr11:77918416
|
CA | C | 6 | a0001c0001t0001g0078a0001c0002t0001g0114a0001c0002t0001g0115others(3): Show | 6 | HG01167.hp2 HG02647.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1922+404delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918416 | ||||||
| chr11:77918464
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1922+357A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918464 | ||||||
| chr11:77918486
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1922+335T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918486 | ||||||
| chr11:77918506
|
G | T | 12 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1922+315C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918506 | ||||||
| chr11:77918507
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1922+314G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918507 | ||||||
| chr11:77918570
|
A | G | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1922+251T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918570 | ||||||
| chr11:77918658
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1922+163A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918658 | ||||||
| chr11:77918659
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1922+162G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918659 | ||||||
| chr11:77918815
|
C | T | 7 | a0001c0001t0001g0307a0001c0001t0001g0343a0001c0001t0001g0344others(4): Show | 7 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1922+6G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 15/22 | chr11 | 77918815 | ||||||
| chr11:77919121
|
T | A | 1 | a0001c0001t0001g0317 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1765-143A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77919121 | ||||||
| chr11:77919298
|
A | AT | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(267): Show | 271 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1765-321dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77919298 | ||||||
| chr11:77919436
|
G | A | 23 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(20): Show | 23 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.1765-458C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77919436 | ||||||
| chr11:77919566
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1765-588C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77919566 | ||||||
| chr11:77919595
|
T | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0354 | 2 | NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1765-617A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77919595 | ||||||
| chr11:77919636
|
G | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1765-658C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77919636 | ||||||
| chr11:77919832
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1765-854C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77919832 | ||||||
| chr11:77920127
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1765-1149T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920127 | ||||||
| chr11:77920154
|
T | TATATACA others(17): Show |
5 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0034others(2): Show | 5 | HG00738.hp2 HG01167.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+1162_1765-117 others(28): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920154 | ||||||
| chr11:77920174
|
T | C | 1 | a0006c0009t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1764+1166A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920174 | ||||||
| chr11:77920178
|
C | CATATACA others(27): Show |
1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1764+1161_1764+116 others(38): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920178 | ||||||
| chr11:77920182
|
T | C | 1 | a0001c0004t0001g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1764+1158A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920182 | ||||||
| chr11:77920198
|
T | C | 77 | a0001c0001t0001g0265a0001c0001t0001g0333a0001c0002t0001g0004others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1764+1142A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920198 | ||||||
| chr11:77920198
|
T | TATACATA others(29): Show |
6 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0309others(3): Show | 6 | HG01074.hp1 NA18747.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1764+1141_1764+114 others(40): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920198 | ||||||
| chr11:77920206
|
C | CACACATA others(5): Show |
6 | a0001c0001t0001g0003a0001c0001t0001g0299a0001c0006t0001g0273others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1764+1122_1764+113 others(16): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920206 | ||||||
| chr11:77920206
|
C | CACACATA others(29): Show |
3 | a0001c0001t0001g0337a0001c0001t0001g0340a0001c0001t0001g0358 | 3 | NA18970.hp2 NA19075.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1764+1133_1764+113 others(40): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920206 | ||||||
| chr11:77920206
|
C | CACACATA others(41): Show |
1 | a0001c0002t0001g0138 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1764+1133_1764+113 others(52): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920206 | ||||||
| chr11:77920206
|
C | CACACATA others(27): Show |
2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1764+1133_1764+113 others(38): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920206 | ||||||
| chr11:77920206
|
C | CACACATA others(17): Show |
58 | a0001c0001t0001g0262a0001c0001t0001g0276a0001c0001t0001g0318others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.1764+1133_1764+113 others(28): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920206 | ||||||
| chr11:77920206
|
C | CACACATA others(29): Show |
61 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0155others(58): Show | 61 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.1764+1133_1764+113 others(40): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920206 | ||||||
| chr11:77920206
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0265others(4): Show | 7 | HG01074.hp1 HG02970.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.1764+1134G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920206 | ||||||
| chr11:77920212
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1764+1127_1764+112 others(28): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920212 | ||||||
| chr11:77920212
|
T | TATATATA others(25): Show |
2 | a0001c0001t0001g0163a0001c0001t0001g0214 | 2 | NA18949.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1764+1127_1764+112 others(36): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920212 | ||||||
| chr11:77920212
|
T | TATATATA others(29): Show |
116 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 117 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1764+1127_1764+112 others(40): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920212 | ||||||
| chr11:77920218
|
T | C | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1764+1122A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920218 | ||||||
| chr11:77920222
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1764+1118G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920222 | ||||||
| chr11:77920226
|
T | TATAC | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1764+1113_1764+111 others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920226 | ||||||
| chr11:77920228
|
C | T | 24 | a0001c0001t0001g0308a0001c0002t0001g0101a0001c0002t0001g0102others(21): Show | 24 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.1764+1112G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920228 | ||||||
| chr11:77920232
|
C | CACAT | 4 | a0001c0002t0001g0101a0001c0002t0001g0302a0001c0002t0001g0303others(1): Show | 4 | HG02622.hp2 NA18973.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1764+1107_1764+110 others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920232 | ||||||
| chr11:77920232
|
C | CACATATA others(19): Show |
17 | a0001c0002t0001g0102a0001c0002t0001g0103a0001c0002t0001g0104others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(14): Show |
intron_variant | MODIFIER | c.1764+1107_1764+110 others(30): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920232 | ||||||
| chr11:77920232
|
C | CACATATA others(27): Show |
2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | HG01070.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1764+1107_1764+110 others(38): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920232 | ||||||
| chr11:77920232
|
C | CACATATA others(39): Show |
1 | a0001c0001t0001g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1764+1107_1764+110 others(50): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920232 | ||||||
| chr11:77920232
|
C | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1764+1108G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920232 | ||||||
| chr11:77920234
|
T | C | 2 | a0001c0004t0001g0254a0001c0004t0001g0255 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1764+1106A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920234 | ||||||
| chr11:77920236
|
T | C | 4 | a0001c0002t0001g0101a0001c0002t0001g0302a0001c0002t0001g0303others(1): Show | 4 | HG02622.hp2 NA18973.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1764+1104A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920236 | ||||||
| chr11:77920238
|
T | C | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1764+1102A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920238 | ||||||
| chr11:77920240
|
C | T | 2 | a0001c0004t0001g0254a0001c0004t0001g0255 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1764+1100G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920240 | ||||||
| chr11:77920242
|
T | TACACATA others(19): Show |
2 | a0001c0004t0001g0254a0001c0004t0001g0255 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1764+1097_1764+109 others(30): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920242 | ||||||
| chr11:77920246
|
T | C | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1764+1094A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920246 | ||||||
| chr11:77920248
|
T | C | 20 | a0001c0001t0001g0308a0001c0002t0001g0092a0001c0002t0001g0093others(17): Show | 20 | HG01070.hp1 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1764+1092A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920248 | ||||||
| chr11:77920250
|
C | T | 19 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0102others(16): Show | 19 | HG01070.hp1 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1764+1090G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920250 | ||||||
| chr11:77920256
|
T | TATAC | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1764+1083_1764+108 others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920256 | ||||||
| chr11:77920258
|
C | CAT | 20 | a0001c0001t0001g0308a0001c0002t0001g0092a0001c0002t0001g0093others(17): Show | 20 | HG01070.hp1 HG02055.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1764+1080_1764+108 others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920258 | ||||||
| chr11:77920258
|
C | CATATATA others(5): Show |
138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0036others(135): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1764+1081_1764+108 others(16): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920258 | ||||||
| chr11:77920258
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(120): Show | 124 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.1764+1082G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920258 | ||||||
| chr11:77920260
|
T | C | 2 | a0001c0004t0001g0254a0001c0004t0001g0255 | 2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1764+1080A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920260 | ||||||
| chr11:77920266
|
C | T | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1764+1074G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920266 | ||||||
| chr11:77920282
|
T | C | 2 | a0001c0002t0001g0150a0001c0002t0001g0300 | 2 | HG01358.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.1764+1058A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920282 | ||||||
| chr11:77920721
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1764+619T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920721 | ||||||
| chr11:77920725
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1764+615C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920725 | ||||||
| chr11:77920954
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0185a0001c0001t0001g0197 | 3 | NA18966.hp2 NA18967.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1764+386G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920954 | ||||||
| chr11:77920979
|
C | A | 1 | a0001c0001t0001g0356 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1764+361G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77920979 | ||||||
| chr11:77921009
|
G | A | 2 | a0001c0002t0001g0114a0001c0002t0001g0116 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1764+331C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77921009 | ||||||
| chr11:77921013
|
A | G | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1764+327T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77921013 | ||||||
| chr11:77921233
|
C | T | 1 | a0002c0003t0001g0292 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1764+107G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77921233 | ||||||
| chr11:77921235
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1764+105C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 14/22 | chr11 | 77921235 | ||||||
| chr11:77921500
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1631-27A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 13/22 | chr11 | 77921500 | ||||||
| chr11:77921849
|
G | A | 1 | a0001c0002t0001g0267 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1631-376C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 13/22 | chr11 | 77921849 | ||||||
| chr11:77922097
|
G | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0286 | 2 | HG01934.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.1630+259C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 13/22 | chr11 | 77922097 | ||||||
| chr11:77922153
|
G | A | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1630+203C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 13/22 | chr11 | 77922153 | ||||||
| chr11:77922228
|
CA | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(258): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1630+127delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 13/22 | chr11 | 77922228 | ||||||
| chr11:77922228
|
CAA | C | 8 | a0001c0001t0001g0010a0001c0001t0001g0162a0001c0001t0001g0183others(5): Show | 8 | HG01167.hp2 HG01496.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1630+126_1630+127d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 13/22 | chr11 | 77922228 | ||||||
| chr11:77922243
|
A | G | 4 | a0001c0001t0001g0082a0001c0001t0001g0189a0003c0005t0001g0099others(1): Show | 4 | HG02559.hp1 HG03139.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.1630+113T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 13/22 | chr11 | 77922243 | ||||||
| chr11:77922478
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | splice_region_variant&intron_variant | LOW | c.1515-7G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77922478 | ||||||
| chr11:77922704
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1515-233A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77922704 | ||||||
| chr11:77922802
|
C | A | 1 | a0001c0001t0001g0356 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1515-331G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77922802 | ||||||
| chr11:77923085
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1515-614G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923085 | ||||||
| chr11:77923109
|
A | G | 2 | a0001c0002t0001g0106a0001c0002t0001g0108 | 2 | NA18963.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1515-638T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923109 | ||||||
| chr11:77923315
|
C | CA | 117 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(114): Show | 118 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.1515-845dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923315 | ||||||
| chr11:77923315
|
C | CAA | 12 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0165others(9): Show | 12 | HG00544.hp1 HG01934.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1515-846_1515-845d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923315 | ||||||
| chr11:77923315
|
CA | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0032others(151): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1515-845delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923315 | ||||||
| chr11:77923349
|
G | T | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1515-878C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923349 | ||||||
| chr11:77923439
|
T | C | 2 | a0001c0002t0001g0124a0001c0002t0001g0125 | 2 | HG02015.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1515-968A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923439 | ||||||
| chr11:77923491
|
T | A | 60 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(57): Show | 60 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1515-1020A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923491 | ||||||
| chr11:77923657
|
G | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0299 | 2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1514+1093C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923657 | ||||||
| chr11:77923766
|
G | GT | 28 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0089others(25): Show | 28 | HG00597.hp1 HG00673.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1514+983dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923766 | ||||||
| chr11:77923766
|
GT | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(105): Show | 109 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.1514+983delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923766 | ||||||
| chr11:77923900
|
G | A | 21 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.1514+850C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923900 | ||||||
| chr11:77923910
|
G | A | 1 | a0001c0001t0001g0275 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1514+840C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923910 | ||||||
| chr11:77923925
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1514+825G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77923925 | ||||||
| chr11:77924011
|
C | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0055a0001c0001t0001g0062 | 3 | HG00738.hp1 HG00741.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1514+739G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77924011 | ||||||
| chr11:77924020
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1514+730G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77924020 | ||||||
| chr11:77924138
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1514+612A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77924138 | ||||||
| chr11:77924232
|
T | TA | 113 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(110): Show | 114 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.1514+517dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77924232 | ||||||
| chr11:77924232
|
T | TAA | 7 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(4): Show | 7 | HG02300.hp2 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1514+516_1514+517d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77924232 | ||||||
| chr11:77924269
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.1514+481T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77924269 | ||||||
| chr11:77924613
|
A | C | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1514+137T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77924613 | ||||||
| chr11:77924662
|
C | A | 12 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(9): Show | 12 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.1514+88G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 12/22 | chr11 | 77924662 | ||||||
| chr11:77924968
|
A | G | 4 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0058others(1): Show | 4 | HG01081.hp1 HG01993.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372-76T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77924968 | ||||||
| chr11:77924969
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1372-77G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77924969 | ||||||
| chr11:77925274
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1372-382G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77925274 | ||||||
| chr11:77925464
|
G | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1372-572C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77925464 | ||||||
| chr11:77925604
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1372-712A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77925604 | ||||||
| chr11:77926022
|
C | T | 27 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(24): Show | 27 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.1372-1130G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926022 | ||||||
| chr11:77926112
|
T | C | 2 | a0001c0002t0001g0092a0001c0002t0001g0093 | 2 | HG01070.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1372-1220A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926112 | ||||||
| chr11:77926189
|
G | GA | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.1372-1298dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926189 | ||||||
| chr11:77926195
|
A | AG | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1372-1304_1372-130 others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926195 | ||||||
| chr11:77926199
|
A | G | 10 | a0001c0002t0001g0106a0001c0002t0001g0107a0001c0002t0001g0108others(7): Show | 10 | HG02602.hp2 HG03654.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.1372-1307T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926199 | ||||||
| chr11:77926322
|
G | T | 3 | a0001c0002t0001g0121a0001c0002t0001g0133a0001c0002t0001g0146 | 3 | HG00099.hp2 HG00639.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1372-1430C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926322 | ||||||
| chr11:77926373
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1372-1481A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926373 | ||||||
| chr11:77926380
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1372-1488C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926380 | ||||||
| chr11:77926381
|
T | C | 3 | a0001c0002t0001g0121a0001c0002t0001g0133a0001c0002t0001g0146 | 3 | HG00099.hp2 HG00639.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1372-1489A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926381 | ||||||
| chr11:77926467
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0266a0001c0001t0002g0097 | 3 | HG02895.hp1 NA18999.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1372-1575C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926467 | ||||||
| chr11:77926524
|
T | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(71): Show | 74 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1372-1632A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926524 | ||||||
| chr11:77926644
|
TA | T | 21 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.1371+1697delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926644 | ||||||
| chr11:77926654
|
A | T | 8 | a0001c0001t0001g0081a0001c0001t0001g0161a0001c0001t0001g0192others(5): Show | 8 | HG02135.hp1 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1371+1688T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926654 | ||||||
| chr11:77926682
|
C | T | 2 | a0001c0002t0001g0094a0001c0002t0001g0095 | 2 | HG00140.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1371+1660G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926682 | ||||||
| chr11:77926759
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(74): Show | 77 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1371+1583G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926759 | ||||||
| chr11:77926809
|
C | A | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1371+1533G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926809 | ||||||
| chr11:77926811
|
CA | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(252): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.1371+1530delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926811 | ||||||
| chr11:77926821
|
AAAAAAGG others(10): Show |
A | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1371+1504_1371+152 others(21): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926821 | ||||||
| chr11:77926822
|
AAAAAGGA others(4): Show |
A | 15 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(12): Show | 15 | HG01975.hp2 HG02056.hp1 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.1371+1509_1371+151 others(15): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926822 | ||||||
| chr11:77926826
|
A | G | 2 | a0001c0001t0001g0003a0001c0002t0001g0127 | 2 | HG01243.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1371+1516T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926826 | ||||||
| chr11:77926827
|
GGAAAGGA others(11): Show |
G | 2 | a0001c0001t0001g0003a0001c0002t0001g0127 | 2 | HG01243.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1371+1497_1371+151 others(22): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926827 | ||||||
| chr11:77926843
|
GAA | G | 16 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(13): Show | 16 | HG01975.hp2 HG02056.hp1 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.1371+1497_1371+149 others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926843 | ||||||
| chr11:77926944
|
C | T | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1371+1398G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926944 | ||||||
| chr11:77926954
|
T | C | 1 | a0001c0002t0001g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1371+1388A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926954 | ||||||
| chr11:77926964
|
G | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0257 | 2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1371+1378C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77926964 | ||||||
| chr11:77927019
|
T | C | 1 | a0001c0002t0001g0146 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1371+1323A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927019 | ||||||
| chr11:77927135
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0036others(76): Show | 79 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1371+1207T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927135 | ||||||
| chr11:77927228
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1371+1114T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927228 | ||||||
| chr11:77927396
|
C | T | 12 | a0001c0001t0001g0262a0001c0001t0001g0318a0001c0001t0001g0321others(9): Show | 12 | HG02257.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1371+946G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927396 | ||||||
| chr11:77927400
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1371+942C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927400 | ||||||
| chr11:77927421
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1371+921A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927421 | ||||||
| chr11:77927501
|
C | T | 1 | a0001c0001t0001g0312 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1371+841G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927501 | ||||||
| chr11:77927510
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1371+832C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927510 | ||||||
| chr11:77927528
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1371+814C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927528 | ||||||
| chr11:77927610
|
C | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1371+732G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927610 | ||||||
| chr11:77927641
|
A | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1371+701T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927641 | ||||||
| chr11:77927698
|
T | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1371+644A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927698 | ||||||
| chr11:77927792
|
T | C | 1 | a0001c0002t0001g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1371+550A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927792 | ||||||
| chr11:77927986
|
C | A | 1 | a0001c0002t0001g0092 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1371+356G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77927986 | ||||||
| chr11:77928074
|
T | C | 74 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(71): Show | 74 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1371+268A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77928074 | ||||||
| chr11:77928223
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1371+119C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77928223 | ||||||
| chr11:77928292
|
CA | C | 4 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0058others(1): Show | 4 | HG01081.hp1 HG01993.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1371+49delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77928292 | ||||||
| chr11:77928336
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp1 | splice_region_variant&intron_variant | LOW | c.1371+6T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 11/22 | chr11 | 77928336 | ||||||
| chr11:77928600
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1166-53C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77928600 | ||||||
| chr11:77928903
|
C | T | 1 | a0006c0009t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1166-356G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77928903 | ||||||
| chr11:77928932
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1166-385C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77928932 | ||||||
| chr11:77928945
|
C | A | 12 | a0001c0001t0001g0262a0001c0001t0001g0318a0001c0001t0001g0321others(9): Show | 12 | HG02257.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1166-398G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77928945 | ||||||
| chr11:77928996
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1166-449C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77928996 | ||||||
| chr11:77929019
|
C | CA | 73 | a0001c0001t0001g0297a0001c0002t0001g0004a0001c0002t0001g0005others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1166-473dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77929019 | ||||||
| chr11:77929074
|
G | A | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1166-527C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77929074 | ||||||
| chr11:77929330
|
T | C | 7 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(4): Show | 7 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1166-783A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77929330 | ||||||
| chr11:77929481
|
G | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1166-934C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77929481 | ||||||
| chr11:77929557
|
C | T | 1 | a0001c0002t0001g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1166-1010G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77929557 | ||||||
| chr11:77929681
|
C | T | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1166-1134G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77929681 | ||||||
| chr11:77930115
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1166-1568G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930115 | ||||||
| chr11:77930227
|
G | A | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1166-1680C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930227 | ||||||
| chr11:77930313
|
A | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0155others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1166-1766T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930313 | ||||||
| chr11:77930419
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1166-1872T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930419 | ||||||
| chr11:77930435
|
A | G | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1166-1888T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930435 | ||||||
| chr11:77930703
|
G | A | 1 | a0001c0002t0001g0122 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1166-2156C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930703 | ||||||
| chr11:77930719
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1166-2172G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930719 | ||||||
| chr11:77930735
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1166-2188A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930735 | ||||||
| chr11:77930766
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1166-2219C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930766 | ||||||
| chr11:77930816
|
TA | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.1166-2270delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930816 | ||||||
| chr11:77930826
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1166-2279A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77930826 | ||||||
| chr11:77931161
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1166-2614C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77931161 | ||||||
| chr11:77931171
|
A | G | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1166-2624T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77931171 | ||||||
| chr11:77931533
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1166-2986C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77931533 | ||||||
| chr11:77931780
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1166-3233T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77931780 | ||||||
| chr11:77931903
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1166-3356G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77931903 | ||||||
| chr11:77931904
|
T | G | 1 | a0001c0001t0001g0306 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1166-3357A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77931904 | ||||||
| chr11:77932064
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1166-3517C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932064 | ||||||
| chr11:77932238
|
T | TA | 74 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1166-3692_1166-369 others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932238 | ||||||
| chr11:77932239
|
C | A | 2 | a0001c0002t0001g0268a0001c0002t0001g0269 | 2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1166-3692G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932239 | ||||||
| chr11:77932240
|
C | A | 74 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1166-3693G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932240 | ||||||
| chr11:77932346
|
A | T | 1 | a0001c0001t0001g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1166-3799T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932346 | ||||||
| chr11:77932349
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1166-3802A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932349 | ||||||
| chr11:77932549
|
C | T | 1 | a0001c0001t0003g0259 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1166-4002G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932549 | ||||||
| chr11:77932667
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1166-4120A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932667 | ||||||
| chr11:77932671
|
A | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1166-4124T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932671 | ||||||
| chr11:77932700
|
C | T | 19 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(16): Show | 19 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.1166-4153G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932700 | ||||||
| chr11:77932929
|
G | C | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1166-4382C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77932929 | ||||||
| chr11:77933078
|
G | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1166-4531C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933078 | ||||||
| chr11:77933134
|
G | A | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1166-4587C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933134 | ||||||
| chr11:77933150
|
A | G | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1166-4603T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933150 | ||||||
| chr11:77933168
|
T | C | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1166-4621A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933168 | ||||||
| chr11:77933228
|
AGTCTCCC others(18): Show |
A | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1166-4706_1166-468 others(29): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933228 | ||||||
| chr11:77933275
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1166-4728G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933275 | ||||||
| chr11:77933330
|
G | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(281): Show | 285 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1166-4783C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933330 | ||||||
| chr11:77933373
|
C | G | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1166-4826G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933373 | ||||||
| chr11:77933374
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1166-4827G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933374 | ||||||
| chr11:77933397
|
AT | A | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(357): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1166-4851delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933397 | ||||||
| chr11:77933434
|
C | T | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1166-4887G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933434 | ||||||
| chr11:77933435
|
G | A | 1 | a0001c0002t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1166-4888C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933435 | ||||||
| chr11:77933489
|
G | T | 1 | a0001c0001t0001g0166 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1166-4942C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933489 | ||||||
| chr11:77933514
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1166-4967C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933514 | ||||||
| chr11:77933597
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1166-5050C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933597 | ||||||
| chr11:77933600
|
C | T | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1165+5051G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933600 | ||||||
| chr11:77933644
|
A | AC | 7 | a0001c0001t0001g0040a0001c0001t0001g0071a0001c0001t0001g0090others(4): Show | 7 | HG02523.hp2 NA18966.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165+5006dupG | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933644 | ||||||
| chr11:77933680
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.1165+4971G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933680 | ||||||
| chr11:77933692
|
G | C | 1 | a0001c0001t0001g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1165+4959C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933692 | ||||||
| chr11:77933778
|
G | A | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1165+4873C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933778 | ||||||
| chr11:77933782
|
G | A | 1 | a0001c0008t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1165+4869C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933782 | ||||||
| chr11:77933792
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1165+4859C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933792 | ||||||
| chr11:77933822
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0299a0001c0002t0001g0091others(4): Show | 7 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1165+4829C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933822 | ||||||
| chr11:77933836
|
G | T | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1165+4815C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933836 | ||||||
| chr11:77933869
|
G | A | 71 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1165+4782C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933869 | ||||||
| chr11:77933880
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(74): Show | 78 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1165+4771G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933880 | ||||||
| chr11:77933890
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1165+4761C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77933890 | ||||||
| chr11:77934018
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1165+4633G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934018 | ||||||
| chr11:77934042
|
T | C | 1 | a0001c0002t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1165+4609A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934042 | ||||||
| chr11:77934053
|
A | AT | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(357): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1165+4597dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934053 | ||||||
| chr11:77934128
|
A | G | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1165+4523T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934128 | ||||||
| chr11:77934141
|
T | C | 24 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(21): Show | 24 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.1165+4510A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934141 | ||||||
| chr11:77934164
|
G | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.1165+4487C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934164 | ||||||
| chr11:77934253
|
C | T | 2 | a0001c0001t0001g0339a0001c0001t0001g0341 | 2 | NA18973.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1165+4398G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934253 | ||||||
| chr11:77934394
|
T | TA | 84 | a0001c0001t0001g0007a0001c0001t0001g0049a0001c0001t0001g0186others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.1165+4256dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934394 | ||||||
| chr11:77934394
|
T | TAA | 112 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(109): Show | 113 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1165+4255_1165+425 others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934394 | ||||||
| chr11:77934394
|
TA | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0036a0001c0001t0001g0054others(3): Show | 6 | HG00597.hp1 HG01081.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165+4256delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934394 | ||||||
| chr11:77934459
|
A | G | 71 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.1165+4192T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934459 | ||||||
| chr11:77934596
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1165+4055A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934596 | ||||||
| chr11:77934604
|
CAAAAATA others(1): Show |
C | 17 | a0001c0001t0001g0206a0001c0001t0001g0262a0001c0001t0001g0318others(14): Show | 17 | HG02257.hp2 HG02451.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1165+4039_1165+404 others(12): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934604 | ||||||
| chr11:77934871
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1165+3780A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77934871 | ||||||
| chr11:77935159
|
G | A | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165+3492C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935159 | ||||||
| chr11:77935316
|
G | A | 1 | a0001c0001t0001g0349 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1165+3335C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935316 | ||||||
| chr11:77935342
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1165+3309G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935342 | ||||||
| chr11:77935470
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(71): Show | 74 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1165+3181C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935470 | ||||||
| chr11:77935881
|
G | A | 3 | a0001c0002t0001g0121a0001c0002t0001g0133a0001c0002t0001g0146 | 3 | HG00099.hp2 HG00639.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1165+2770C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935881 | ||||||
| chr11:77935903
|
A | AAAAAAAA others(15): Show |
1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1165+2747_1165+274 others(26): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935903 | ||||||
| chr11:77935903
|
A | AAAAAAAA others(14): Show |
2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1165+2747_1165+274 others(25): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935903 | ||||||
| chr11:77935903
|
A | AAAAAAAG others(13): Show |
275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1165+2747_1165+274 others(24): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935903 | ||||||
| chr11:77935903
|
A | AAAAAAGA others(12): Show |
6 | a0001c0002t0001g0091a0001c0002t0001g0126a0001c0004t0001g0252others(3): Show | 6 | HG01168.hp1 HG02451.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1165+2747_1165+274 others(23): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935903 | ||||||
| chr11:77935911
|
A | AAAAGAAA others(13): Show |
2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1165+2739_1165+274 others(24): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77935911 | ||||||
| chr11:77936154
|
AAGGATGG others(9): Show |
A | 76 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0047others(73): Show | 76 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1165+2481_1165+249 others(20): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77936154 | ||||||
| chr11:77936227
|
GA | G | 21 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.1165+2423delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77936227 | ||||||
| chr11:77936604
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1165+2047G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77936604 | ||||||
| chr11:77936836
|
C | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(21): Show | 24 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.1165+1815G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77936836 | ||||||
| chr11:77936903
|
G | A | 1 | a0003c0005t0001g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1165+1748C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77936903 | ||||||
| chr11:77936986
|
A | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(199): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1165+1665T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77936986 | ||||||
| chr11:77937042
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1165+1609C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937042 | ||||||
| chr11:77937256
|
G | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0205 | 2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1165+1395C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937256 | ||||||
| chr11:77937301
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1165+1350A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937301 | ||||||
| chr11:77937469
|
C | T | 1 | a0004c0010t0001g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1165+1182G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937469 | ||||||
| chr11:77937636
|
C | T | 70 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.1165+1015G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937636 | ||||||
| chr11:77937703
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1165+948G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937703 | ||||||
| chr11:77937817
|
G | GTATT | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0036others(68): Show | 71 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.1165+830_1165+833d others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937817 | ||||||
| chr11:77937817
|
G | GTATTTAT others(1): Show |
15 | a0001c0001t0001g0266a0001c0001t0001g0286a0001c0001t0001g0299others(12): Show | 15 | HG00280.hp1 HG02523.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1165+826_1165+833d others(10): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937817 | ||||||
| chr11:77937817
|
G | GTATTTAT others(5): Show |
1 | a0001c0001t0001g0321 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1165+822_1165+833d others(14): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937817 | ||||||
| chr11:77937817
|
GTATT | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1165+830_1165+833d others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937817 | ||||||
| chr11:77937817
|
GTATTTAT others(5): Show |
G | 25 | a0001c0001t0001g0157a0001c0001t0001g0199a0001c0001t0001g0222others(22): Show | 25 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.1165+822_1165+833d others(14): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937817 | ||||||
| chr11:77937817
|
GTATTTAT others(9): Show |
G | 172 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(169): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1165+818_1165+833d others(18): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937817 | ||||||
| chr11:77937910
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG02615.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1165+741G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77937910 | ||||||
| chr11:77938191
|
G | C | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165+460C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77938191 | ||||||
| chr11:77938273
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1165+378T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77938273 | ||||||
| chr11:77938318
|
T | G | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1165+333A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77938318 | ||||||
| chr11:77938487
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1165+164G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 10/22 | chr11 | 77938487 | ||||||
| chr11:77939088
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.991-263C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939088 | ||||||
| chr11:77939193
|
C | T | 1 | a0001c0002t0001g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.991-368G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939193 | ||||||
| chr11:77939274
|
G | C | 1 | a0001c0001t0001g0222 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.991-449C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939274 | ||||||
| chr11:77939421
|
C | CG | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-597dupC | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939421 | ||||||
| chr11:77939752
|
A | T | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.991-927T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939752 | ||||||
| chr11:77939821
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.991-996C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939821 | ||||||
| chr11:77939823
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0331 | 2 | HG00408.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.991-998G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939823 | ||||||
| chr11:77939848
|
C | CA | 72 | a0001c0001t0001g0036a0001c0001t0001g0073a0001c0001t0001g0098others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.991-1024dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939848 | ||||||
| chr11:77939852
|
A | C | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-1027T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939852 | ||||||
| chr11:77939856
|
A | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(195): Show | 199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.991-1031T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939856 | ||||||
| chr11:77939877
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.991-1052T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77939877 | ||||||
| chr11:77940010
|
C | T | 281 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(278): Show | 282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.990+1170G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940010 | ||||||
| chr11:77940054
|
A | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.990+1126T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940054 | ||||||
| chr11:77940145
|
G | A | 69 | a0001c0001t0001g0036a0001c0001t0001g0155a0001c0001t0001g0260others(66): Show | 69 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.990+1035C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940145 | ||||||
| chr11:77940282
|
T | A | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.990+898A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940282 | ||||||
| chr11:77940323
|
C | G | 1 | a0001c0002t0001g0281 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.990+857G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940323 | ||||||
| chr11:77940516
|
T | C | 1 | a0001c0002t0001g0142 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.990+664A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940516 | ||||||
| chr11:77940531
|
G | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0072 | 2 | HG03669.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.990+649C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940531 | ||||||
| chr11:77940621
|
T | G | 1 | a0001c0001t0001g0057 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.990+559A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940621 | ||||||
| chr11:77940627
|
G | T | 269 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(266): Show | 270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.990+553C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940627 | ||||||
| chr11:77940663
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.990+517C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940663 | ||||||
| chr11:77940697
|
T | G | 1 | a0001c0001t0001g0178 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.990+483A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940697 | ||||||
| chr11:77940740
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.990+440A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940740 | ||||||
| chr11:77940782
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.990+398C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77940782 | ||||||
| chr11:77941085
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.990+95T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 9/22 | chr11 | 77941085 | ||||||
| chr11:77941374
|
C | T | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.919-123G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77941374 | ||||||
| chr11:77941458
|
C | CT | 193 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(190): Show | 193 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.919-208dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77941458 | ||||||
| chr11:77941458
|
C | CTT | 82 | a0001c0001t0001g0214a0001c0001t0001g0283a0001c0001t0001g0284others(79): Show | 82 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.919-209_919-208dup others(2): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77941458 | ||||||
| chr11:77941841
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.919-590C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77941841 | ||||||
| chr11:77942310
|
G | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(273): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.919-1059C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77942310 | ||||||
| chr11:77942359
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.919-1108G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77942359 | ||||||
| chr11:77942542
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-1291G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77942542 | ||||||
| chr11:77942637
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.919-1386A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77942637 | ||||||
| chr11:77942743
|
C | G | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.919-1492G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77942743 | ||||||
| chr11:77942921
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.919-1670T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77942921 | ||||||
| chr11:77943102
|
T | C | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.919-1851A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77943102 | ||||||
| chr11:77943187
|
C | T | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.919-1936G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77943187 | ||||||
| chr11:77943192
|
G | C | 1 | a0001c0001t0001g0272 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.919-1941C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77943192 | ||||||
| chr11:77943206
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.919-1955G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77943206 | ||||||
| chr11:77943649
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0217 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.919-2398A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77943649 | ||||||
| chr11:77943819
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.919-2568T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77943819 | ||||||
| chr11:77943909
|
T | C | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.919-2658A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77943909 | ||||||
| chr11:77944047
|
T | C | 21 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(18): Show |
intron_variant | MODIFIER | c.919-2796A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944047 | ||||||
| chr11:77944219
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.919-2968A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944219 | ||||||
| chr11:77944259
|
G | A | 1 | a0001c0001t0001g0360 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.919-3008C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944259 | ||||||
| chr11:77944294
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.919-3043G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944294 | ||||||
| chr11:77944574
|
G | A | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.919-3323C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944574 | ||||||
| chr11:77944594
|
C | T | 1 | a0001c0001t0001g0316 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.919-3343G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944594 | ||||||
| chr11:77944595
|
G | A | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.919-3344C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944595 | ||||||
| chr11:77944616
|
C | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0195 | 3 | HG02622.hp1 HG02897.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.919-3365G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944616 | ||||||
| chr11:77944626
|
C | G | 1 | a0001c0001t0001g0220 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.919-3375G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944626 | ||||||
| chr11:77944635
|
G | A | 69 | a0001c0001t0001g0036a0001c0001t0001g0155a0001c0001t0001g0260others(66): Show | 69 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.919-3384C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944635 | ||||||
| chr11:77944716
|
T | C | 1 | a0001c0002t0001g0303 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.919-3465A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944716 | ||||||
| chr11:77944812
|
G | A | 71 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.919-3561C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77944812 | ||||||
| chr11:77945231
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.919-3980G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945231 | ||||||
| chr11:77945313
|
A | T | 2 | a0001c0001t0001g0265a0001c0004t0001g0252 | 2 | HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.919-4062T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945313 | ||||||
| chr11:77945423
|
G | A | 3 | a0001c0004t0001g0253a0001c0004t0001g0254a0001c0004t0001g0255 | 3 | HG02451.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.919-4172C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945423 | ||||||
| chr11:77945424
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.919-4173A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945424 | ||||||
| chr11:77945446
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.919-4195A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945446 | ||||||
| chr11:77945453
|
C | G | 1 | a0001c0001t0001g0169 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.919-4202G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945453 | ||||||
| chr11:77945633
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.919-4382C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945633 | ||||||
| chr11:77945708
|
C | G | 1 | a0001c0002t0001g0136 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.919-4457G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945708 | ||||||
| chr11:77945727
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18969.hp1 NA19074.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.919-4476T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945727 | ||||||
| chr11:77945848
|
C | A | 13 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0173others(10): Show | 13 | HG00544.hp1 HG02027.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.919-4597G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945848 | ||||||
| chr11:77945873
|
C | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-4622G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77945873 | ||||||
| chr11:77946035
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.919-4784G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946035 | ||||||
| chr11:77946425
|
G | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(5): Show | 8 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.919-5174C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946425 | ||||||
| chr11:77946520
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0155others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.919-5269C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946520 | ||||||
| chr11:77946574
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.919-5323G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946574 | ||||||
| chr11:77946618
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.919-5367C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946618 | ||||||
| chr11:77946693
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.919-5442C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946693 | ||||||
| chr11:77946730
|
C | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0155others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.919-5479G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946730 | ||||||
| chr11:77946760
|
C | CA | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0020others(89): Show | 92 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.919-5510dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946760 | ||||||
| chr11:77946813
|
C | T | 8 | a0001c0001t0001g0306a0001c0001t0001g0320a0001c0001t0001g0337others(5): Show | 8 | NA18970.hp2 NA18973.hp2 NA18993.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-5562G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946813 | ||||||
| chr11:77946876
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0155others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.919-5625T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946876 | ||||||
| chr11:77946914
|
C | CA | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(357): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.919-5664dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77946914 | ||||||
| chr11:77947075
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.919-5824A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947075 | ||||||
| chr11:77947091
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.919-5840G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947091 | ||||||
| chr11:77947126
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.919-5875C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947126 | ||||||
| chr11:77947218
|
G | C | 1 | a0001c0001t0001g0014 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.919-5967C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947218 | ||||||
| chr11:77947244
|
A | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.919-5993T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947244 | ||||||
| chr11:77947315
|
A | G | 1 | a0001c0002t0001g0118 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.919-6064T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947315 | ||||||
| chr11:77947462
|
C | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(272): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.919-6211G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947462 | ||||||
| chr11:77947545
|
C | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0240 | 3 | NA18942.hp2 NA19077.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.919-6294G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947545 | ||||||
| chr11:77947546
|
A | C | 2 | a0001c0001t0001g0344a0001c0001t0001g0345 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.919-6295T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947546 | ||||||
| chr11:77947550
|
A | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.919-6299T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947550 | ||||||
| chr11:77947630
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.919-6379T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947630 | ||||||
| chr11:77947793
|
T | A | 1 | a0001c0001t0001g0277 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.919-6542A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77947793 | ||||||
| chr11:77948176
|
GA | G | 70 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(67): Show | 70 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.919-6926delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948176 | ||||||
| chr11:77948310
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.919-7059A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948310 | ||||||
| chr11:77948325
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0155others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.919-7074G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948325 | ||||||
| chr11:77948372
|
C | T | 1 | a0001c0002t0001g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.919-7121G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948372 | ||||||
| chr11:77948466
|
T | G | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.919-7215A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948466 | ||||||
| chr11:77948475
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG01934.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.919-7224C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948475 | ||||||
| chr11:77948509
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.919-7258T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948509 | ||||||
| chr11:77948533
|
G | A | 1 | a0001c0002t0001g0151 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.919-7282C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948533 | ||||||
| chr11:77948534
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.919-7283C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948534 | ||||||
| chr11:77948564
|
T | C | 1 | a0001c0001t0001g0199 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.919-7313A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948564 | ||||||
| chr11:77948598
|
G | A | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.918+7344C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948598 | ||||||
| chr11:77948654
|
CA | C | 6 | a0001c0001t0001g0098a0001c0001t0001g0279a0001c0001t0001g0351others(3): Show | 6 | HG01074.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+7287delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948654 | ||||||
| chr11:77948654
|
CAA | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.918+7286_918+7287d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948654 | ||||||
| chr11:77948655
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0002t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.918+7274_918+7286d others(15): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948655 | ||||||
| chr11:77948658
|
AAAAAAAA others(3): Show |
A | 55 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(52): Show | 55 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.918+7274_918+7283d others(12): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948658 | ||||||
| chr11:77948659
|
AAAAAAAA others(2): Show |
A | 14 | a0001c0002t0001g0118a0001c0002t0001g0122a0001c0002t0001g0134others(11): Show | 14 | HG00408.hp1 HG00609.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.918+7274_918+7282d others(11): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948659 | ||||||
| chr11:77948678
|
AAAG | A | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 204 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.918+7261_918+7263d others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948678 | ||||||
| chr11:77948694
|
AAGG | A | 73 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.918+7245_918+7247d others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948694 | ||||||
| chr11:77948697
|
G | A | 1 | a0001c0002t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.918+7245C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948697 | ||||||
| chr11:77948703
|
A | T | 20 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(17): Show | 20 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.918+7239T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948703 | ||||||
| chr11:77948791
|
GA | G | 80 | a0001c0001t0001g0316a0001c0001t0001g0347a0001c0001t0001g0348others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.918+7150delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948791 | ||||||
| chr11:77948809
|
T | C | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+7133A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948809 | ||||||
| chr11:77948937
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0068 | 2 | HG00738.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.918+7005T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77948937 | ||||||
| chr11:77949000
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.918+6942G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949000 | ||||||
| chr11:77949009
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.918+6933G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949009 | ||||||
| chr11:77949055
|
GC | G | 4 | a0001c0002t0001g0123a0001c0002t0001g0124a0001c0002t0001g0125others(1): Show | 4 | HG00673.hp2 HG02015.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+6886delG | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949055 | ||||||
| chr11:77949073
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0116 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.918+6869G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949073 | ||||||
| chr11:77949117
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0155others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.918+6825T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949117 | ||||||
| chr11:77949473
|
C | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0280 | 2 | NA18939.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.918+6469G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949473 | ||||||
| chr11:77949519
|
C | CA | 106 | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0001g0061others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.918+6422dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949519 | ||||||
| chr11:77949521
|
A | G | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.918+6421T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949521 | ||||||
| chr11:77949537
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.918+6405G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949537 | ||||||
| chr11:77949637
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.918+6305A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949637 | ||||||
| chr11:77949716
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+6226T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949716 | ||||||
| chr11:77949763
|
T | C | 3 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | NA19005.hp2 NA19068.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.918+6179A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949763 | ||||||
| chr11:77949984
|
T | C | 1 | a0003c0005t0001g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.918+5958A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77949984 | ||||||
| chr11:77950133
|
C | T | 4 | a0001c0002t0001g0300a0001c0002t0001g0302a0001c0002t0001g0303others(1): Show | 4 | NA18973.hp1 NA18994.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+5809G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950133 | ||||||
| chr11:77950159
|
T | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.918+5783A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950159 | ||||||
| chr11:77950228
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.918+5714G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950228 | ||||||
| chr11:77950353
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.918+5589G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950353 | ||||||
| chr11:77950472
|
G | A | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.918+5470C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950472 | ||||||
| chr11:77950617
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.918+5325C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950617 | ||||||
| chr11:77950686
|
C | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0299others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+5256G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950686 | ||||||
| chr11:77950698
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.918+5244G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950698 | ||||||
| chr11:77950718
|
TTTTG | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.918+5220_918+5223d others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950718 | ||||||
| chr11:77950759
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.918+5183T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950759 | ||||||
| chr11:77950761
|
G | C | 1 | a0001c0001t0001g0251 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.918+5181C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950761 | ||||||
| chr11:77950805
|
T | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.918+5137A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950805 | ||||||
| chr11:77950813
|
C | T | 1 | a0001c0002t0001g0122 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.918+5129G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950813 | ||||||
| chr11:77950851
|
T | G | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.918+5091A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950851 | ||||||
| chr11:77950874
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.918+5068G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950874 | ||||||
| chr11:77950969
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.918+4973C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77950969 | ||||||
| chr11:77951234
|
G | T | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.918+4708C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951234 | ||||||
| chr11:77951268
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.918+4674A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951268 | ||||||
| chr11:77951316
|
G | T | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.918+4626C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951316 | ||||||
| chr11:77951378
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.918+4564A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951378 | ||||||
| chr11:77951421
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0192 | 2 | NA18948.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.918+4521A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951421 | ||||||
| chr11:77951438
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0012 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+4504C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951438 | ||||||
| chr11:77951456
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(192): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.918+4486G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951456 | ||||||
| chr11:77951533
|
A | C | 1 | a0001c0002t0001g0004 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.918+4409T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951533 | ||||||
| chr11:77951766
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0338 | 2 | NA18949.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.918+4176G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951766 | ||||||
| chr11:77951782
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(192): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.918+4160A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951782 | ||||||
| chr11:77951863
|
A | T | 1 | a0003c0005t0001g0099 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.918+4079T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77951863 | ||||||
| chr11:77952181
|
G | A | 2 | a0001c0002t0001g0094a0001c0002t0001g0095 | 2 | HG00140.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.918+3761C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77952181 | ||||||
| chr11:77952505
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.918+3437A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77952505 | ||||||
| chr11:77952569
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.918+3373A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77952569 | ||||||
| chr11:77952599
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.918+3343T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77952599 | ||||||
| chr11:77952805
|
A | G | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0196others(1): Show | 4 | HG02132.hp2 NA18968.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+3137T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77952805 | ||||||
| chr11:77953110
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.918+2832G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953110 | ||||||
| chr11:77953338
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.918+2604A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953338 | ||||||
| chr11:77953369
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.918+2573A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953369 | ||||||
| chr11:77953587
|
A | AT | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.918+2354dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953587 | ||||||
| chr11:77953615
|
G | A | 2 | a0001c0004t0001g0252a0001c0004t0001g0253 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.918+2327C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953615 | ||||||
| chr11:77953623
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.918+2319C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953623 | ||||||
| chr11:77953652
|
C | T | 37 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(34): Show | 37 | HG00140.hp2 HG00544.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.918+2290G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953652 | ||||||
| chr11:77953694
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.918+2248G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953694 | ||||||
| chr11:77953808
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.918+2134A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953808 | ||||||
| chr11:77953882
|
G | T | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.918+2060C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953882 | ||||||
| chr11:77953986
|
G | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 123 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.918+1956C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77953986 | ||||||
| chr11:77954055
|
G | A | 1 | a0001c0001t0001g0249 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.918+1887C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954055 | ||||||
| chr11:77954151
|
A | G | 3 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0296 | 3 | NA18968.hp2 NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.918+1791T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954151 | ||||||
| chr11:77954153
|
A | C | 2 | a0001c0001t0001g0098a0001c0002t0001g0112 | 2 | HG01074.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.918+1789T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954153 | ||||||
| chr11:77954284
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.918+1658T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954284 | ||||||
| chr11:77954292
|
A | T | 7 | a0001c0002t0001g0113a0001c0002t0001g0114a0001c0002t0001g0115others(4): Show | 7 | HG01496.hp2 HG02647.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+1650T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954292 | ||||||
| chr11:77954293
|
A | T | 75 | a0001c0001t0001g0054a0001c0002t0001g0004a0001c0002t0001g0005others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.918+1649T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954293 | ||||||
| chr11:77954294
|
T | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.918+1648A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954294 | ||||||
| chr11:77954295
|
T | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 97 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.918+1647A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954295 | ||||||
| chr11:77954296
|
T | A | 4 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0202others(1): Show | 4 | HG02280.hp1 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+1646A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954296 | ||||||
| chr11:77954350
|
G | T | 2 | a0003c0005t0001g0099a0003c0005t0001g0100 | 2 | HG02559.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.918+1592C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954350 | ||||||
| chr11:77954501
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.918+1441A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954501 | ||||||
| chr11:77954560
|
C | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(21): Show | 24 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.918+1382G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954560 | ||||||
| chr11:77954682
|
C | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.918+1260G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954682 | ||||||
| chr11:77954771
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0241 | 2 | HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.918+1171A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954771 | ||||||
| chr11:77954847
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.918+1095G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954847 | ||||||
| chr11:77954848
|
C | A | 71 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.918+1094G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954848 | ||||||
| chr11:77954848
|
C | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 126 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.918+1094G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954848 | ||||||
| chr11:77954877
|
A | T | 1 | a0004c0010t0001g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.918+1065T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954877 | ||||||
| chr11:77954914
|
T | A | 1 | a0001c0002t0001g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.918+1028A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77954914 | ||||||
| chr11:77955035
|
CTTTCTAT others(20): Show |
C | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG01358.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.918+880_918+906del others(27): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77955035 | ||||||
| chr11:77955262
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.918+680C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77955262 | ||||||
| chr11:77955441
|
C | T | 74 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.918+501G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77955441 | ||||||
| chr11:77955496
|
C | CT | 61 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0023others(58): Show | 61 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.918+445dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77955496 | ||||||
| chr11:77955598
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.918+344G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77955598 | ||||||
| chr11:77955601
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.918+341A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77955601 | ||||||
| chr11:77955645
|
G | A | 5 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(2): Show | 5 | HG02622.hp2 HG02630.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+297C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77955645 | ||||||
| chr11:77955775
|
TGA | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.918+165_918+166del others(2): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 8/22 | chr11 | 77955775 | ||||||
| chr11:77956298
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.798-236G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956298 | ||||||
| chr11:77956352
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(272): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.798-290T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956352 | ||||||
| chr11:77956394
|
C | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.798-332G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956394 | ||||||
| chr11:77956547
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.798-485T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956547 | ||||||
| chr11:77956636
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.798-574A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956636 | ||||||
| chr11:77956710
|
AAAT | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0033a0001c0001t0001g0046others(13): Show | 16 | HG01081.hp1 HG01243.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.798-651_798-649del others(3): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956710 | ||||||
| chr11:77956710
|
AAATAAT | A | 45 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.798-654_798-649del others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956710 | ||||||
| chr11:77956710
|
AAATAATA others(2): Show |
A | 7 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 7 | HG01081.hp2 HG01884.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.798-657_798-649del others(9): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956710 | ||||||
| chr11:77956710
|
AAATAATA others(5): Show |
A | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02145.hp1 HG02615.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.798-660_798-649del others(12): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956710 | ||||||
| chr11:77956710
|
AAATAATA others(8): Show |
A | 2 | a0001c0001t0001g0081a0001c0001t0001g0329 | 2 | HG03486.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.798-663_798-649del others(15): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956710 | ||||||
| chr11:77956710
|
AAATAATA others(11): Show |
A | 76 | a0001c0001t0001g0002a0001c0001t0001g0077a0001c0001t0001g0155others(73): Show | 76 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.798-666_798-649del others(18): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956710 | ||||||
| chr11:77956710
|
AAATAATA others(14): Show |
A | 127 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(124): Show | 128 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.798-669_798-649del others(21): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956710 | ||||||
| chr11:77956710
|
AAATAATA others(26): Show |
A | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.798-681_798-649del others(33): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956710 | ||||||
| chr11:77956711
|
AATAATAA others(13): Show |
A | 1 | a0001c0001t0001g0227 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.798-669_798-650del others(20): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956711 | ||||||
| chr11:77956712
|
ATAATAAT others(15): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.798-672_798-651del others(22): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956712 | ||||||
| chr11:77956734
|
T | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.798-672A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956734 | ||||||
| chr11:77956737
|
T | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.798-675A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956737 | ||||||
| chr11:77956740
|
T | A | 7 | a0001c0001t0001g0191a0001c0001t0001g0219a0001c0001t0001g0233others(4): Show | 7 | HG01433.hp2 HG02027.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.798-678A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956740 | ||||||
| chr11:77956765
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.798-703T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956765 | ||||||
| chr11:77956933
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.798-871C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956933 | ||||||
| chr11:77956973
|
C | T | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.798-911G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77956973 | ||||||
| chr11:77957028
|
G | T | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.798-966C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957028 | ||||||
| chr11:77957080
|
G | A | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.798-1018C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957080 | ||||||
| chr11:77957115
|
T | C | 1 | a0001c0002t0001g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.798-1053A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957115 | ||||||
| chr11:77957301
|
C | A | 1 | a0001c0001t0001g0329 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.798-1239G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957301 | ||||||
| chr11:77957378
|
A | G | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.798-1316T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957378 | ||||||
| chr11:77957459
|
A | G | 1 | a0001c0001t0001g0347 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.797+1287T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957459 | ||||||
| chr11:77957486
|
G | T | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.797+1260C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957486 | ||||||
| chr11:77957636
|
AGTTTATT others(7): Show |
A | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.797+1096_797+1109d others(16): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957636 | ||||||
| chr11:77957663
|
C | CT | 59 | a0001c0001t0001g0090a0001c0001t0001g0175a0001c0001t0001g0193others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.797+1082dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957663 | ||||||
| chr11:77957663
|
C | CTT | 19 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(16): Show | 19 | HG01358.hp2 HG02055.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.797+1081_797+1082d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957663 | ||||||
| chr11:77957663
|
CT | C | 24 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(21): Show | 24 | HG00323.hp2 HG01069.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.797+1082delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957663 | ||||||
| chr11:77957711
|
C | A | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.797+1035G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957711 | ||||||
| chr11:77957720
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.797+1026C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957720 | ||||||
| chr11:77957814
|
G | A | 14 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(11): Show | 15 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.797+932C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77957814 | ||||||
| chr11:77958071
|
T | C | 5 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.797+675A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77958071 | ||||||
| chr11:77958195
|
A | T | 1 | a0001c0001t0001g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.797+551T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77958195 | ||||||
| chr11:77958224
|
T | A | 3 | a0001c0002t0001g0114a0001c0002t0001g0115a0001c0002t0001g0116 | 3 | HG02647.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.797+522A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77958224 | ||||||
| chr11:77958738
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | splice_region_variant&intron_variant | LOW | c.797+8T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 7/22 | chr11 | 77958738 | ||||||
| chr11:77958939
|
A | G | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.709-105T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77958939 | ||||||
| chr11:77959066
|
A | G | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.709-232T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77959066 | ||||||
| chr11:77959133
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.709-299G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77959133 | ||||||
| chr11:77959191
|
C | T | 76 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.709-357G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77959191 | ||||||
| chr11:77959217
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.709-383G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77959217 | ||||||
| chr11:77959388
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.709-554T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77959388 | ||||||
| chr11:77959421
|
T | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.709-587A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77959421 | ||||||
| chr11:77959539
|
C | A | 1 | a0001c0001t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.709-705G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77959539 | ||||||
| chr11:77959907
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.708+434G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77959907 | ||||||
| chr11:77959936
|
T | C | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.708+405A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77959936 | ||||||
| chr11:77960095
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 277 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.708+246A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77960095 | ||||||
| chr11:77960095
|
T | G | 7 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(4): Show | 7 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.708+246A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77960095 | ||||||
| chr11:77960171
|
A | G | 71 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.708+170T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77960171 | ||||||
| chr11:77960204
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.708+137G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77960204 | ||||||
| chr11:77960235
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.708+106T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 6/22 | chr11 | 77960235 | ||||||
| chr11:77960498
|
T | C | 71 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.658-107A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 5/22 | chr11 | 77960498 | ||||||
| chr11:77960586
|
T | C | 1 | a0001c0002t0001g0110 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.658-195A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 5/22 | chr11 | 77960586 | ||||||
| chr11:77960596
|
C | G | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-205G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 5/22 | chr11 | 77960596 | ||||||
| chr11:77960777
|
C | CA | 5 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(2): Show | 5 | NA18942.hp2 NA18946.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+175dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 5/22 | chr11 | 77960777 | ||||||
| chr11:77960822
|
C | T | 199 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(196): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.657+131G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 5/22 | chr11 | 77960822 | ||||||
| chr11:77960876
|
T | C | 1 | a0001c0002t0001g0118 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.657+77A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 5/22 | chr11 | 77960876 | ||||||
| chr11:77961143
|
T | TA | 115 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(112): Show | 116 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(113): Show |
splice_region_variant&intron_variant | LOW | c.472-6dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961143 | ||||||
| chr11:77961143
|
T | TAA | 72 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(69): Show | 72 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(69): Show |
splice_region_variant&intron_variant | LOW | c.472-7_472-6dupTT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961143 | ||||||
| chr11:77961153
|
A | AAAAAAAA others(3): Show |
1 | a0004c0010t0001g0109 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.472-16_472-15insCT others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961153 | ||||||
| chr11:77961196
|
A | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0039others(7): Show | 10 | HG00609.hp2 HG01192.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.472-58T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961196 | ||||||
| chr11:77961268
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.472-130A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961268 | ||||||
| chr11:77961443
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.472-305C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961443 | ||||||
| chr11:77961494
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.472-356A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961494 | ||||||
| chr11:77961506
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.472-368A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961506 | ||||||
| chr11:77961624
|
T | C | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-486A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961624 | ||||||
| chr11:77961670
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0069a0001c0001t0001g0080 | 3 | HG02083.hp1 NA18612.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.472-532A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961670 | ||||||
| chr11:77961819
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0155others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.472-681T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961819 | ||||||
| chr11:77961992
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.472-854A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77961992 | ||||||
| chr11:77962212
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.472-1074C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77962212 | ||||||
| chr11:77962264
|
CAG | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.472-1128_472-1127d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77962264 | ||||||
| chr11:77962268
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.472-1130C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77962268 | ||||||
| chr11:77962646
|
C | A | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-1508G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77962646 | ||||||
| chr11:77962794
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.472-1656G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77962794 | ||||||
| chr11:77962852
|
TA | T | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.472-1715delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77962852 | ||||||
| chr11:77962980
|
A | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.472-1842T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77962980 | ||||||
| chr11:77963238
|
T | C | 16 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(13): Show | 16 | HG01975.hp2 HG02056.hp1 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.472-2100A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963238 | ||||||
| chr11:77963316
|
T | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.472-2178A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963316 | ||||||
| chr11:77963317
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.472-2179C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963317 | ||||||
| chr11:77963352
|
C | CA | 99 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0027others(96): Show | 99 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.472-2215dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963352 | ||||||
| chr11:77963352
|
C | CAA | 30 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(27): Show | 30 | HG00738.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.472-2216_472-2215d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963352 | ||||||
| chr11:77963366
|
A | C | 9 | a0001c0001t0001g0306a0001c0001t0001g0320a0001c0001t0001g0337others(6): Show | 9 | NA18949.hp2 NA18970.hp2 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.472-2228T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963366 | ||||||
| chr11:77963368
|
A | AC | 75 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(72): Show | 76 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.472-2231_472-2230i others(3): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963368 | ||||||
| chr11:77963368
|
A | C | 1 | a0001c0004t0001g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.472-2230T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963368 | ||||||
| chr11:77963369
|
A | AAAAAAAA others(5): Show |
1 | a0003c0005t0001g0100 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.472-2232_472-2231i others(14): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963369 | ||||||
| chr11:77963370
|
AAAAAC | A | 13 | a0001c0002t0001g0094a0001c0002t0001g0101a0001c0002t0001g0102others(10): Show | 13 | HG00140.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.472-2237_472-2233d others(7): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963370 | ||||||
| chr11:77963371
|
AAAAC | A | 46 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(43): Show | 46 | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.472-2237_472-2234d others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963371 | ||||||
| chr11:77963372
|
AAAC | A | 15 | a0001c0002t0001g0092a0001c0002t0001g0093a0001c0002t0001g0113others(12): Show | 15 | HG00609.hp1 HG01070.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.472-2237_472-2235d others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963372 | ||||||
| chr11:77963375
|
C | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0228a0001c0001t0001g0232others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-2237G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963375 | ||||||
| chr11:77963717
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.472-2579A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77963717 | ||||||
| chr11:77964168
|
A | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.472-3030T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964168 | ||||||
| chr11:77964289
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0076 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.472-3151G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964289 | ||||||
| chr11:77964339
|
G | A | 23 | a0001c0001t0001g0157a0001c0001t0001g0222a0001c0001t0001g0223others(20): Show | 23 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.472-3201C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964339 | ||||||
| chr11:77964413
|
A | T | 20 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(17): Show | 20 | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(17): Show |
intron_variant | MODIFIER | c.472-3275T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964413 | ||||||
| chr11:77964499
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.472-3361T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964499 | ||||||
| chr11:77964564
|
ACT | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.472-3428_472-3427d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964564 | ||||||
| chr11:77964579
|
T | A | 1 | a0001c0001t0001g0243 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.472-3441A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964579 | ||||||
| chr11:77964591
|
T | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.472-3453A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964591 | ||||||
| chr11:77964677
|
G | A | 80 | a0001c0001t0001g0251a0001c0002t0001g0004a0001c0002t0001g0005others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.472-3539C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964677 | ||||||
| chr11:77964830
|
C | T | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-3692G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964830 | ||||||
| chr11:77964837
|
G | C | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-3699C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964837 | ||||||
| chr11:77964899
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.472-3761A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964899 | ||||||
| chr11:77964915
|
A | T | 3 | a0001c0001t0001g0317a0001c0001t0001g0330a0001c0001t0001g0336 | 3 | HG02523.hp1 NA18991.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.472-3777T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77964915 | ||||||
| chr11:77965033
|
T | C | 2 | a0001c0002t0001g0281a0001c0002t0001g0291 | 2 | NA18961.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.472-3895A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965033 | ||||||
| chr11:77965081
|
A | C | 73 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0155others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.472-3943T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965081 | ||||||
| chr11:77965180
|
A | G | 1 | a0001c0001t0001g0028 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.472-4042T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965180 | ||||||
| chr11:77965210
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.472-4072G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965210 | ||||||
| chr11:77965225
|
T | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.472-4087A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965225 | ||||||
| chr11:77965232
|
G | A | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.472-4094C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965232 | ||||||
| chr11:77965264
|
C | A | 4 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(1): Show | 5 | HG00323.hp1 HG01261.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.472-4126G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965264 | ||||||
| chr11:77965385
|
G | A | 2 | a0001c0001t0001g0278a0001c0001t0001g0280 | 2 | NA18939.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.472-4247C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965385 | ||||||
| chr11:77965599
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.472-4461G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965599 | ||||||
| chr11:77965775
|
T | C | 1 | a0001c0001t0001g0313 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.472-4637A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965775 | ||||||
| chr11:77965786
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.472-4648A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965786 | ||||||
| chr11:77965821
|
A | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0017others(2): Show | 6 | HG00323.hp1 HG01074.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-4683T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965821 | ||||||
| chr11:77965842
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.472-4704C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965842 | ||||||
| chr11:77965973
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(272): Show | 276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.472-4835T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965973 | ||||||
| chr11:77965978
|
C | T | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-4840G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77965978 | ||||||
| chr11:77966137
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.472-4999A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77966137 | ||||||
| chr11:77966349
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.472-5211A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77966349 | ||||||
| chr11:77966435
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.472-5297C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77966435 | ||||||
| chr11:77966438
|
T | C | 1 | a0001c0001t0001g0355 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.472-5300A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77966438 | ||||||
| chr11:77966654
|
T | C | 1 | a0001c0002t0001g0142 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.472-5516A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77966654 | ||||||
| chr11:77966782
|
A | C | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-5644T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77966782 | ||||||
| chr11:77966887
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.472-5749A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77966887 | ||||||
| chr11:77967018
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.472-5880G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77967018 | ||||||
| chr11:77967039
|
T | A | 1 | a0001c0001t0001g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.472-5901A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77967039 | ||||||
| chr11:77967344
|
C | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.472-6206G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77967344 | ||||||
| chr11:77967377
|
C | G | 1 | a0001c0001t0001g0260 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.472-6239G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77967377 | ||||||
| chr11:77967390
|
C | T | 1 | a0001c0008t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.472-6252G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77967390 | ||||||
| chr11:77967495
|
C | T | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.472-6357G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77967495 | ||||||
| chr11:77967531
|
T | C | 1 | a0001c0002t0001g0143 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.472-6393A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77967531 | ||||||
| chr11:77967758
|
T | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.472-6620A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77967758 | ||||||
| chr11:77967973
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.472-6835A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77967973 | ||||||
| chr11:77968212
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0257 | 2 | HG02015.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.472-7074G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77968212 | ||||||
| chr11:77968301
|
T | C | 4 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0278others(1): Show | 4 | HG02071.hp1 NA18939.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-7163A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77968301 | ||||||
| chr11:77968340
|
T | C | 1 | a0001c0002t0001g0144 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.472-7202A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77968340 | ||||||
| chr11:77968504
|
G | A | 1 | a0001c0002t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.472-7366C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77968504 | ||||||
| chr11:77968708
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.472-7570A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77968708 | ||||||
| chr11:77968825
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.472-7687T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77968825 | ||||||
| chr11:77968887
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.472-7749A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77968887 | ||||||
| chr11:77969081
|
T | A | 1 | a0001c0002t0001g0108 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.472-7943A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969081 | ||||||
| chr11:77969189
|
C | T | 10 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0039others(7): Show | 10 | HG00609.hp2 HG01192.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.472-8051G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969189 | ||||||
| chr11:77969353
|
G | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 90 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.472-8215C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969353 | ||||||
| chr11:77969355
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.472-8217C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969355 | ||||||
| chr11:77969412
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0155others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.472-8274C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969412 | ||||||
| chr11:77969602
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(55): Show | 58 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.472-8464C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969602 | ||||||
| chr11:77969668
|
C | G | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-8530G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969668 | ||||||
| chr11:77969764
|
C | CA | 31 | a0001c0001t0001g0098a0001c0001t0001g0157a0001c0001t0001g0193others(28): Show | 31 | HG00735.hp1 HG01074.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.472-8627dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969764 | ||||||
| chr11:77969799
|
C | G | 2 | a0001c0001t0001g0266a0001c0001t0002g0097 | 2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.472-8661G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969799 | ||||||
| chr11:77969824
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.472-8686C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77969824 | ||||||
| chr11:77970024
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | NA18963.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.472-8886G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970024 | ||||||
| chr11:77970130
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0116 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.471+8866G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970130 | ||||||
| chr11:77970147
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0155others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.471+8849T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970147 | ||||||
| chr11:77970194
|
C | T | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.471+8802G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970194 | ||||||
| chr11:77970195
|
G | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.471+8801C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970195 | ||||||
| chr11:77970372
|
T | C | 1 | a0001c0002t0001g0096 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.471+8624A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970372 | ||||||
| chr11:77970458
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.471+8538A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970458 | ||||||
| chr11:77970470
|
A | C | 1 | a0001c0002t0001g0120 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.471+8526T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970470 | ||||||
| chr11:77970528
|
T | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.471+8468A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970528 | ||||||
| chr11:77970553
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.471+8443C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970553 | ||||||
| chr11:77970898
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.471+8098T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970898 | ||||||
| chr11:77970915
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.471+8081G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77970915 | ||||||
| chr11:77971028
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01167.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.471+7968C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971028 | ||||||
| chr11:77971088
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.471+7908C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971088 | ||||||
| chr11:77971233
|
C | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(115): Show | 119 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.471+7763G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971233 | ||||||
| chr11:77971374
|
G | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+7622C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971374 | ||||||
| chr11:77971387
|
C | G | 2 | a0001c0002t0001g0114a0001c0002t0001g0116 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.471+7609G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971387 | ||||||
| chr11:77971475
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.471+7521G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971475 | ||||||
| chr11:77971637
|
C | T | 1 | a0001c0008t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.471+7359G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971637 | ||||||
| chr11:77971678
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.471+7318A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971678 | ||||||
| chr11:77971803
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.471+7193G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971803 | ||||||
| chr11:77971836
|
A | C | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(282): Show | 286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.471+7160T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971836 | ||||||
| chr11:77971851
|
T | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.471+7145A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77971851 | ||||||
| chr11:77972081
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.471+6915A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972081 | ||||||
| chr11:77972273
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0155others(70): Show | 73 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.471+6723T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972273 | ||||||
| chr11:77972374
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.471+6622G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972374 | ||||||
| chr11:77972418
|
CT | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(199): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.471+6577delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972418 | ||||||
| chr11:77972676
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.471+6320G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972676 | ||||||
| chr11:77972696
|
C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0217 | 3 | HG02280.hp1 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.471+6300G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972696 | ||||||
| chr11:77972774
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.471+6222T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972774 | ||||||
| chr11:77972782
|
A | G | 1 | a0001c0002t0001g0300 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.471+6214T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972782 | ||||||
| chr11:77972831
|
G | GT | 11 | a0001c0001t0001g0073a0001c0001t0001g0266a0001c0001t0001g0270others(8): Show | 11 | HG00597.hp2 HG01175.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.471+6164dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972831 | ||||||
| chr11:77972831
|
GT | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.471+6164delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972831 | ||||||
| chr11:77972989
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.471+6007A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77972989 | ||||||
| chr11:77973090
|
C | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.471+5906G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973090 | ||||||
| chr11:77973192
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.471+5804A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973192 | ||||||
| chr11:77973203
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.471+5793A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973203 | ||||||
| chr11:77973334
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.471+5662C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973334 | ||||||
| chr11:77973374
|
T | C | 1 | a0001c0001t0001g0239 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.471+5622A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973374 | ||||||
| chr11:77973467
|
T | C | 1 | a0001c0001t0001g0357 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.471+5529A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973467 | ||||||
| chr11:77973577
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 283 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.471+5419T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973577 | ||||||
| chr11:77973598
|
A | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | NA18953.hp1 NA18954.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.471+5398T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973598 | ||||||
| chr11:77973601
|
C | A | 1 | a0001c0001t0001g0243 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.471+5395G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973601 | ||||||
| chr11:77973610
|
T | G | 1 | a0001c0002t0001g0103 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.471+5386A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973610 | ||||||
| chr11:77973801
|
T | G | 1 | a0001c0001t0001g0350 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.471+5195A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973801 | ||||||
| chr11:77973893
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.471+5103A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973893 | ||||||
| chr11:77973902
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0155others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.471+5094G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77973902 | ||||||
| chr11:77974058
|
G | A | 2 | a0001c0002t0001g0281a0001c0002t0001g0291 | 2 | NA18961.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.471+4938C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974058 | ||||||
| chr11:77974178
|
T | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(200): Show | 204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.471+4818A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974178 | ||||||
| chr11:77974196
|
TTAAC | T | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+4796_471+4799d others(6): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974196 | ||||||
| chr11:77974228
|
TTTTTC | T | 12 | a0001c0001t0001g0008a0001c0001t0001g0021a0001c0001t0001g0164others(9): Show | 12 | HG00140.hp2 HG01346.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+4763_471+4767d others(7): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974228 | ||||||
| chr11:77974233
|
CTTTTCT | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(102): Show | 106 | HG00323.hp1 HG00544.hp1 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.471+4757_471+4762d others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974233 | ||||||
| chr11:77974238
|
CT | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0074others(145): Show | 148 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.471+4757delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974238 | ||||||
| chr11:77974238
|
CTT | C | 7 | a0001c0001t0001g0284a0001c0001t0001g0285a0001c0001t0001g0341others(4): Show | 7 | HG00733.hp2 HG01069.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+4756_471+4757d others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974238 | ||||||
| chr11:77974245
|
T | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0251a0001c0001t0001g0265others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.471+4751A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974245 | ||||||
| chr11:77974246
|
T | C | 1 | a0001c0002t0001g0116 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.471+4750A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974246 | ||||||
| chr11:77974248
|
T | A | 71 | a0001c0001t0001g0251a0001c0002t0001g0004a0001c0002t0001g0005others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.471+4748A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974248 | ||||||
| chr11:77974389
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.471+4607G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974389 | ||||||
| chr11:77974431
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.471+4565G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974431 | ||||||
| chr11:77974530
|
T | C | 5 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+4466A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974530 | ||||||
| chr11:77974551
|
CATA | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.471+4442_471+4444d others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974551 | ||||||
| chr11:77974602
|
CT | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.471+4393delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974602 | ||||||
| chr11:77974655
|
T | C | 9 | a0001c0001t0001g0306a0001c0001t0001g0320a0001c0001t0001g0337others(6): Show | 9 | NA18949.hp2 NA18970.hp2 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.471+4341A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974655 | ||||||
| chr11:77974889
|
C | T | 7 | a0001c0001t0001g0307a0001c0001t0001g0343a0001c0001t0001g0344others(4): Show | 7 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+4107G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974889 | ||||||
| chr11:77974890
|
G | A | 50 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.471+4106C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974890 | ||||||
| chr11:77974902
|
A | G | 5 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272others(2): Show | 5 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+4094T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974902 | ||||||
| chr11:77974923
|
T | C | 1 | a0001c0002t0001g0145 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.471+4073A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974923 | ||||||
| chr11:77974950
|
T | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.471+4046A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77974950 | ||||||
| chr11:77975167
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.471+3829T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975167 | ||||||
| chr11:77975324
|
G | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0357 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.471+3672C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975324 | ||||||
| chr11:77975332
|
A | G | 1 | a0001c0001t0001g0316 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.471+3664T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975332 | ||||||
| chr11:77975342
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.471+3654A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975342 | ||||||
| chr11:77975681
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0206others(1): Show | 4 | HG01928.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+3315C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975681 | ||||||
| chr11:77975705
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+3291G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975705 | ||||||
| chr11:77975729
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.471+3267C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975729 | ||||||
| chr11:77975942
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.471+3054G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975942 | ||||||
| chr11:77975955
|
C | CA | 28 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 29 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.471+3040dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975955 | ||||||
| chr11:77975955
|
CA | C | 71 | a0001c0001t0001g0215a0001c0002t0001g0004a0001c0002t0001g0005others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.471+3040delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975955 | ||||||
| chr11:77975994
|
A | C | 2 | a0001c0002t0001g0112a0001c0002t0001g0113 | 2 | HG01496.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.471+3002T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77975994 | ||||||
| chr11:77976121
|
A | AT | 95 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.471+2874dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77976121 | ||||||
| chr11:77976152
|
T | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.471+2844A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77976152 | ||||||
| chr11:77976480
|
C | T | 3 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227 | 3 | NA19011.hp1 NA19063.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.471+2516G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77976480 | ||||||
| chr11:77976691
|
G | A | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.471+2305C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77976691 | ||||||
| chr11:77976769
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.471+2227G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77976769 | ||||||
| chr11:77976941
|
G | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.471+2055C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77976941 | ||||||
| chr11:77977198
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0155others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.471+1798G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77977198 | ||||||
| chr11:77977395
|
C | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.471+1601G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77977395 | ||||||
| chr11:77977565
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0239 | 3 | NA18942.hp2 NA18977.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.471+1431T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77977565 | ||||||
| chr11:77977611
|
T | C | 2 | a0001c0006t0001g0273a0001c0006t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.471+1385A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77977611 | ||||||
| chr11:77977692
|
T | C | 1 | a0001c0002t0001g0111 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.471+1304A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77977692 | ||||||
| chr11:77977728
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.471+1268T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77977728 | ||||||
| chr11:77977894
|
T | G | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.471+1102A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77977894 | ||||||
| chr11:77977975
|
G | A | 7 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(4): Show | 7 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+1021C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77977975 | ||||||
| chr11:77977978
|
T | C | 4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0196others(1): Show | 4 | HG02132.hp2 NA18968.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+1018A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77977978 | ||||||
| chr11:77978046
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.471+950C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77978046 | ||||||
| chr11:77978118
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.471+878G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77978118 | ||||||
| chr11:77978243
|
T | C | 1 | a0001c0002t0001g0146 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.471+753A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77978243 | ||||||
| chr11:77978251
|
G | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.471+745C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77978251 | ||||||
| chr11:77978655
|
G | A | 1 | a0001c0001t0001g0002 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.471+341C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77978655 | ||||||
| chr11:77978740
|
G | GA | 4 | a0001c0002t0001g0147a0001c0002t0001g0148a0001c0002t0001g0149others(1): Show | 4 | HG00733.hp1 HG01167.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+255dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77978740 | ||||||
| chr11:77978833
|
T | C | 6 | a0001c0001t0001g0307a0001c0001t0001g0343a0001c0001t0001g0344others(3): Show | 6 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+163A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77978833 | ||||||
| chr11:77978965
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.471+31C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 4/22 | chr11 | 77978965 | ||||||
| chr11:77979116
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.365-14A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979116 | ||||||
| chr11:77979218
|
C | A | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.365-116G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979218 | ||||||
| chr11:77979375
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0002t0001g0120 | 3 | HG00738.hp1 HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.365-273G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979375 | ||||||
| chr11:77979380
|
T | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.365-278A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979380 | ||||||
| chr11:77979432
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.365-330C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979432 | ||||||
| chr11:77979507
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.365-405T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979507 | ||||||
| chr11:77979605
|
A | G | 5 | a0001c0001t0001g0316a0001c0001t0001g0347a0001c0001t0001g0348others(2): Show | 5 | HG00597.hp2 NA18612.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.365-503T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979605 | ||||||
| chr11:77979680
|
G | GA | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0098others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.365-579dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979680 | ||||||
| chr11:77979727
|
C | T | 4 | a0001c0002t0001g0101a0001c0002t0001g0102a0001c0002t0001g0103others(1): Show | 4 | HG02622.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.365-625G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979727 | ||||||
| chr11:77979751
|
G | A | 12 | a0001c0001t0001g0262a0001c0001t0001g0318a0001c0001t0001g0321others(9): Show | 12 | HG02257.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.365-649C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979751 | ||||||
| chr11:77979796
|
G | A | 13 | a0001c0001t0001g0261a0001c0001t0001g0305a0001c0001t0001g0316others(10): Show | 13 | HG00597.hp2 HG02080.hp1 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.365-694C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979796 | ||||||
| chr11:77979849
|
G | A | 1 | a0001c0002t0001g0256 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.365-747C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979849 | ||||||
| chr11:77979850
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(199): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.365-748A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979850 | ||||||
| chr11:77979892
|
C | A | 2 | a0001c0001t0001g0003a0001c0001t0001g0299 | 2 | HG01243.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.365-790G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979892 | ||||||
| chr11:77979893
|
G | A | 1 | a0001c0001t0001g0355 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.365-791C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979893 | ||||||
| chr11:77979913
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.365-811C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979913 | ||||||
| chr11:77979956
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.365-854G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979956 | ||||||
| chr11:77979977
|
CA | C | 6 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0173others(3): Show | 6 | HG01167.hp1 HG02135.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.365-876delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77979977 | ||||||
| chr11:77980002
|
C | T | 195 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(192): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.365-900G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980002 | ||||||
| chr11:77980004
|
GA | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(198): Show | 202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.365-903delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980004 | ||||||
| chr11:77980006
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.365-904T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980006 | ||||||
| chr11:77980063
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.365-961T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980063 | ||||||
| chr11:77980154
|
C | T | 1 | a0001c0001t0001g0317 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.365-1052G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980154 | ||||||
| chr11:77980179
|
CT | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(199): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.365-1078delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980179 | ||||||
| chr11:77980359
|
T | C | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.364+1100A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980359 | ||||||
| chr11:77980373
|
ATTTTT | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0155others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.364+1081_364+1085d others(7): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980373 | ||||||
| chr11:77980386
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.364+1073T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980386 | ||||||
| chr11:77980448
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0205 | 2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.364+1011A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980448 | ||||||
| chr11:77980719
|
A | C | 120 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(117): Show | 121 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.364+740T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980719 | ||||||
| chr11:77980719
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0098others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.364+740T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980719 | ||||||
| chr11:77980929
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.364+530G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77980929 | ||||||
| chr11:77981018
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.364+441G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77981018 | ||||||
| chr11:77981190
|
CA | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(225): Show | 229 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.364+268delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77981190 | ||||||
| chr11:77981254
|
G | A | 1 | a0005c0007t0001g0079 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.364+205C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77981254 | ||||||
| chr11:77981288
|
G | C | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.364+171C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 3/22 | chr11 | 77981288 | ||||||
| chr11:77981729
|
G | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0266others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.247-153C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981729 | ||||||
| chr11:77981738
|
C | CATTT | 50 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(47): Show | 50 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.247-163_247-162ins others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981738 | ||||||
| chr11:77981738
|
C | CATTTATT others(1): Show |
18 | a0001c0001t0001g0283a0001c0001t0001g0285a0001c0001t0001g0286others(15): Show | 18 | HG00544.hp2 HG02257.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.247-163_247-162ins others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981738 | ||||||
| chr11:77981738
|
C | CATTTATT others(5): Show |
2 | a0001c0001t0001g0284a0001c0001t0001g0318 | 2 | HG03041.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.247-163_247-162ins others(12): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981738 | ||||||
| chr11:77981739
|
T | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.247-163A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981739 | ||||||
| chr11:77981739
|
T | TTTTA | 5 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0084others(2): Show | 5 | HG01074.hp1 HG02970.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-167_247-164dup others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981739 | ||||||
| chr11:77981739
|
T | TTTTATTT others(5): Show |
2 | a0001c0001t0001g0299a0003c0005t0001g0100 | 2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.247-175_247-164dup others(12): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981739 | ||||||
| chr11:77981739
|
T | TTTTATTT others(9): Show |
1 | a0001c0001t0001g0003 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.247-179_247-164dup others(16): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981739 | ||||||
| chr11:77981739
|
TTTTA | T | 106 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(103): Show | 106 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.247-167_247-164del others(4): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981739 | ||||||
| chr11:77981739
|
TTTTATTT others(1): Show |
T | 75 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.247-171_247-164del others(8): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981739 | ||||||
| chr11:77981739
|
TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0172 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-179_247-164del others(16): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981739 | ||||||
| chr11:77981769
|
TTA | T | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-195_247-194del others(2): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77981769 | ||||||
| chr11:77982128
|
C | T | 24 | a0001c0001t0001g0157a0001c0001t0001g0166a0001c0001t0001g0222others(21): Show | 24 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.247-552G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982128 | ||||||
| chr11:77982136
|
C | CT | 9 | a0001c0001t0001g0085a0001c0001t0001g0265a0001c0001t0001g0278others(6): Show | 9 | HG02071.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.247-561dupA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982136 | ||||||
| chr11:77982136
|
CT | C | 22 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0032others(19): Show | 22 | HG01070.hp1 HG01074.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.247-561delA | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982136 | ||||||
| chr11:77982169
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.247-593T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982169 | ||||||
| chr11:77982226
|
C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(199): Show | 203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.247-650G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982226 | ||||||
| chr11:77982310
|
T | A | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-734A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982310 | ||||||
| chr11:77982355
|
C | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 122 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.247-779G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982355 | ||||||
| chr11:77982371
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247-795G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982371 | ||||||
| chr11:77982389
|
T | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.247-813A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982389 | ||||||
| chr11:77982390
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.247-814C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982390 | ||||||
| chr11:77982430
|
G | A | 2 | a0001c0001t0001g0262a0001c0001t0001g0357 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.247-854C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982430 | ||||||
| chr11:77982533
|
C | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.247-957G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982533 | ||||||
| chr11:77982618
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.247-1042A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77982618 | ||||||
| chr11:77983316
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.247-1740T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77983316 | ||||||
| chr11:77983416
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.247-1840G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77983416 | ||||||
| chr11:77983421
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.247-1845T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77983421 | ||||||
| chr11:77983456
|
A | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(205): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.247-1880T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77983456 | ||||||
| chr11:77983486
|
C | A | 1 | a0001c0001t0001g0205 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.247-1910G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77983486 | ||||||
| chr11:77983498
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.247-1922G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77983498 | ||||||
| chr11:77983616
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.247-2040G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77983616 | ||||||
| chr11:77983922
|
T | C | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2346A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77983922 | ||||||
| chr11:77983964
|
A | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01167.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.247-2388T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77983964 | ||||||
| chr11:77984150
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.247-2574A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77984150 | ||||||
| chr11:77984201
|
T | C | 1 | a0001c0001t0001g0358 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.247-2625A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77984201 | ||||||
| chr11:77984340
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.247-2764T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77984340 | ||||||
| chr11:77984508
|
A | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0265a0001c0001t0001g0299others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-2932T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77984508 | ||||||
| chr11:77984509
|
A | T | 5 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0114others(2): Show | 5 | HG01496.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.247-2933T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77984509 | ||||||
| chr11:77984636
|
A | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0272 | 2 | HG01884.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.247-3060T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77984636 | ||||||
| chr11:77984848
|
C | T | 74 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.247-3272G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77984848 | ||||||
| chr11:77984914
|
G | GA | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.247-3339dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77984914 | ||||||
| chr11:77985026
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.247-3450G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77985026 | ||||||
| chr11:77985041
|
A | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01123.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.247-3465T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77985041 | ||||||
| chr11:77985448
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18979.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.247-3872G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77985448 | ||||||
| chr11:77985727
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.247-4151T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77985727 | ||||||
| chr11:77985741
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | NA18969.hp1 NA19074.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.247-4165C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77985741 | ||||||
| chr11:77985863
|
G | A | 1 | a0001c0001t0001g0315 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.247-4287C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77985863 | ||||||
| chr11:77985981
|
T | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG01975.hp1 HG02071.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-4405A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77985981 | ||||||
| chr11:77986116
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.247-4540C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77986116 | ||||||
| chr11:77986194
|
T | A | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-4618A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77986194 | ||||||
| chr11:77986205
|
G | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.247-4629C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77986205 | ||||||
| chr11:77986360
|
G | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0251a0001c0001t0001g0265others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.246+4748C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77986360 | ||||||
| chr11:77986648
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.246+4460A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77986648 | ||||||
| chr11:77986825
|
C | T | 1 | a0001c0002t0001g0118 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.246+4283G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77986825 | ||||||
| chr11:77987076
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.246+4032G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987076 | ||||||
| chr11:77987254
|
T | A | 1 | a0001c0001t0001g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.246+3854A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987254 | ||||||
| chr11:77987255
|
A | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0165others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.246+3853T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987255 | ||||||
| chr11:77987472
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.246+3636A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987472 | ||||||
| chr11:77987478
|
C | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.246+3630G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987478 | ||||||
| chr11:77987551
|
C | T | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+3557G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987551 | ||||||
| chr11:77987605
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.246+3503A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987605 | ||||||
| chr11:77987648
|
T | C | 50 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.246+3460A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987648 | ||||||
| chr11:77987846
|
T | C | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+3262A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987846 | ||||||
| chr11:77987935
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.246+3173G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77987935 | ||||||
| chr11:77988010
|
GCCAGTCT others(6): Show |
G | 15 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(12): Show | 16 | HG00323.hp1 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.246+3085_246+3097d others(15): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77988010 | ||||||
| chr11:77988041
|
A | G | 76 | a0001c0001t0001g0251a0001c0002t0001g0004a0001c0002t0001g0005others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.246+3067T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77988041 | ||||||
| chr11:77988046
|
C | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.246+3062G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77988046 | ||||||
| chr11:77988108
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0098others(152): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.246+3000G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77988108 | ||||||
| chr11:77988462
|
T | A | 1 | a0001c0001t0001g0359 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.246+2646A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77988462 | ||||||
| chr11:77988564
|
G | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0272 | 3 | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.246+2544C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77988564 | ||||||
| chr11:77988936
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+2172G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77988936 | ||||||
| chr11:77989106
|
A | G | 87 | a0001c0001t0001g0003a0001c0001t0001g0251a0001c0001t0001g0265others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.246+2002T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77989106 | ||||||
| chr11:77989132
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.246+1976T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77989132 | ||||||
| chr11:77989134
|
C | A | 1 | a0001c0002t0001g0150 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.246+1974G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77989134 | ||||||
| chr11:77989151
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0155others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.246+1957C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77989151 | ||||||
| chr11:77989214
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0155others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.246+1894C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77989214 | ||||||
| chr11:77989215
|
C | T | 1 | a0001c0002t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.246+1893G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77989215 | ||||||
| chr11:77989216
|
G | A | 4 | a0001c0004t0001g0252a0001c0004t0001g0253a0001c0004t0001g0254others(1): Show | 4 | HG02451.hp2 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+1892C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77989216 | ||||||
| chr11:77989800
|
G | C | 1 | a0001c0001t0001g0360 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.246+1308C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77989800 | ||||||
| chr11:77990163
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.246+945C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990163 | ||||||
| chr11:77990215
|
C | CA | 9 | a0001c0001t0001g0090a0001c0001t0001g0158a0001c0001t0001g0159others(6): Show | 9 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+892dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990215 | ||||||
| chr11:77990215
|
C | CAA | 74 | a0001c0001t0001g0265a0001c0002t0001g0004a0001c0002t0001g0005others(71): Show | 74 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.246+891_246+892dup others(2): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990215 | ||||||
| chr11:77990215
|
C | CAAA | 12 | a0001c0001t0001g0003a0001c0001t0001g0266a0001c0001t0001g0299others(9): Show | 12 | HG01243.hp1 HG01496.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+890_246+892dup others(3): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990215 | ||||||
| chr11:77990215
|
CA | C | 74 | a0001c0001t0001g0007a0001c0001t0001g0098a0001c0001t0001g0155others(71): Show | 74 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.246+892delT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990215 | ||||||
| chr11:77990281
|
C | T | 5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(2): Show | 5 | HG00639.hp1 HG02486.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+827G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990281 | ||||||
| chr11:77990629
|
C | T | 72 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0155others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.246+479G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990629 | ||||||
| chr11:77990672
|
C | T | 1 | a0001c0002t0001g0091 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.246+436G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990672 | ||||||
| chr11:77990686
|
C | CA | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(130): Show | 134 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.246+421dupT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990686 | ||||||
| chr11:77990686
|
C | CAA | 61 | a0001c0001t0001g0098a0001c0001t0001g0155a0001c0001t0001g0214others(58): Show | 61 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.246+420_246+421dup others(2): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990686 | ||||||
| chr11:77990747
|
G | C | 1 | a0001c0001t0001g0299 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+361C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990747 | ||||||
| chr11:77990799
|
G | A | 1 | a0001c0002t0001g0154 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.246+309C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990799 | ||||||
| chr11:77990815
|
T | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(189): Show | 193 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.246+293A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990815 | ||||||
| chr11:77990838
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0299a0003c0005t0001g0099others(1): Show | 4 | HG01243.hp1 HG02559.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+270C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990838 | ||||||
| chr11:77990987
|
T | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 279 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.246+121A>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 2/22 | chr11 | 77990987 | ||||||
| chr11:77991438
|
G | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0251a0001c0001t0001g0265others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.55-139C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77991438 | ||||||
| chr11:77991589
|
A | C | 1 | a0001c0001t0001g0002 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.55-290T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77991589 | ||||||
| chr11:77991632
|
G | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0155others(69): Show | 72 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.55-333C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77991632 | ||||||
| chr11:77991815
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0098a0001c0001t0001g0155others(72): Show | 75 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.55-516A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77991815 | ||||||
| chr11:77991819
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.55-520C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77991819 | ||||||
| chr11:77991834
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.55-535A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77991834 | ||||||
| chr11:77991914
|
C | T | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.55-615G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77991914 | ||||||
| chr11:77991921
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(116): Show | 120 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.55-622G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77991921 | ||||||
| chr11:77992153
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.55-854A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992153 | ||||||
| chr11:77992172
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 96 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.55-873G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992172 | ||||||
| chr11:77992204
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.55-905G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992204 | ||||||
| chr11:77992272
|
C | T | 76 | a0001c0001t0001g0251a0001c0002t0001g0004a0001c0002t0001g0005others(73): Show | 76 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.55-973G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992272 | ||||||
| chr11:77992304
|
T | C | 50 | a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0091others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.55-1005A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992304 | ||||||
| chr11:77992349
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.55-1050G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992349 | ||||||
| chr11:77992482
|
C | T | 1 | a0001c0008t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.55-1183G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992482 | ||||||
| chr11:77992484
|
T | G | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.55-1185A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992484 | ||||||
| chr11:77992548
|
T | TAATAA | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | NA18962.hp2 NA18977.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.55-1254_55-1250dup others(5): Show |
INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992548 | ||||||
| chr11:77992587
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.55-1288C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992587 | ||||||
| chr11:77992626
|
A | T | 6 | a0001c0001t0001g0003a0001c0001t0001g0266a0001c0001t0001g0299others(3): Show | 6 | HG01243.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-1327T>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992626 | ||||||
| chr11:77992644
|
G | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0098others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.55-1345C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992644 | ||||||
| chr11:77992831
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.55-1532G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992831 | ||||||
| chr11:77992831
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.55-1532G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992831 | ||||||
| chr11:77992937
|
C | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0155a0001c0001t0001g0260others(68): Show | 71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.55-1638G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77992937 | ||||||
| chr11:77993093
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.54+1497T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993093 | ||||||
| chr11:77993230
|
G | A | 1 | a0001c0002t0001g0291 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.54+1360C>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993230 | ||||||
| chr11:77993236
|
G | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0098others(149): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.54+1354C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993236 | ||||||
| chr11:77993239
|
A | G | 3 | a0001c0002t0001g0094a0001c0002t0001g0095a0001c0002t0001g0096 | 3 | HG00140.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.54+1351T>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993239 | ||||||
| chr11:77993245
|
A | C | 3 | a0001c0002t0001g0091a0001c0002t0001g0092a0001c0002t0001g0093 | 3 | HG01070.hp1 HG01168.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.54+1345T>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993245 | ||||||
| chr11:77993519
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.54+1071G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993519 | ||||||
| chr11:77993546
|
C | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0098others(260): Show | 263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.54+1044G>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993546 | ||||||
| chr11:77993646
|
T | TA | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0098others(261): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.54+943_54+944insT | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993646 | ||||||
| chr11:77993975
|
AG | A | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0258others(67): Show | 70 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.54+614delC | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993975 | ||||||
| chr11:77993981
|
T | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.54+609A>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77993981 | ||||||
| chr11:77994168
|
T | C | 10 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0270others(7): Show | 10 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+422A>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77994168 | ||||||
| chr11:77994490
|
C | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0275a0001c0001t0001g0276others(85): Show | 88 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.54+100G>T | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77994490 | ||||||
| chr11:77994568
|
G | T | 1 | a0001c0001t0001g0003 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.54+22C>A | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77994568 | ||||||
| chr11:77994578
|
G | C | 1 | a0001c0001t0001g0002 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.54+12C>G | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77994578 | ||||||
| chr11:77994579
|
C | G | 1 | a0001c0001t0001g0002 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.54+11G>C | INTS4 | ENSG00000149262.19 | transcript | ENST00000534064.6 | protein_coding | 1/22 | chr11 | 77994579 |