| geneid | 768211 |
|---|---|
| ensemblid | ENSG00000181826.10 |
| hgncid | 27379 |
| symbol | RELL1 |
| name | RELT like 1 |
| refseq_nuc | NM_001085400.2 |
| refseq_prot | NP_001078869.1 |
| ensembl_nuc | ENST00000454158.7 |
| ensembl_prot | ENSP00000398778.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 37610634 |
| end | 37686376 |
| strand | - |
| ver | v1.2 |
| region | chr4:37610634-37686376 |
| region5000 | chr4:37605634-37691376 |
| regionname0 | RELL1_chr4_37610634_37686376 |
| regionname5000 | RELL1_chr4_37605634_37691376 |
| 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 | 271 | 318 | 78 | 64 | 120 | 15 | 39 | 81 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0002 | 0/0 | 271 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0003 | 0/0 | 271 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0004 | 0/0 | 271 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0005 | 0/0 | 271 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| 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 | 816 | 305 | 67 | 63 | 120 | 15 | 38 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| c0002 | 0/0 | 816 | 6 | 5 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| c0003 | 0/0 | 816 | 4 | 4 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| c0004 | 0/0 | 816 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| c0005 | 0/0 | 816 | 2 | 0 | 0 | 1 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| c0006 | 0/0 | 816 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| c0007 | 0/0 | 816 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| c0008 | 0/0 | 816 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| c0009 | 0/0 | 816 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2798 | 64 | 12 | 14 | 25 | 5 | 7 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0002 | 0/0 | 2798 | 36 | 2 | 6 | 26 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0003 | 0/0 | 2803 | 33 | 0 | 2 | 28 | 0 | 3 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0004 | 0/0 | 2802 | 31 | 3 | 12 | 0 | 7 | 9 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0005 | 0/0 | 2799 | 18 | 16 | 2 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0006 | 0/0 | 2789 | 13 | 0 | 4 | 6 | 0 | 3 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0007 | 0/0 | 2799 | 8 | 2 | 1 | 1 | 2 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0008 | 0/0 | 2800 | 7 | 5 | 1 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0009 | 0/0 | 2799 | 5 | 1 | 0 | 4 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0010 | 0/0 | 2803 | 4 | 0 | 0 | 4 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0011 | 0/0 | 2787 | 4 | 3 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0012 | 0/0 | 2793 | 4 | 4 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0013 | 0/0 | 2793 | 4 | 0 | 3 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0014 | 0/0 | 2788 | 4 | 0 | 0 | 1 | 0 | 3 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0015 | 0/0 | 2804 | 4 | 0 | 2 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0016 | 0/0 | 2797 | 3 | 0 | 2 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0017 | 0/0 | 2802 | 3 | 1 | 0 | 0 | 1 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0018 | 0/0 | 2800 | 3 | 1 | 2 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0019 | 0/0 | 2800 | 3 | 3 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0020 | 0/0 | 2802 | 3 | 3 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0021 | 0/0 | 2803 | 3 | 0 | 1 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0022 | 0/0 | 2798 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0023 | 0/0 | 2797 | 2 | 0 | 0 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0024 | 0/0 | 2799 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0025 | 0/0 | 2798 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0026 | 0/0 | 2798 | 2 | 1 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0027 | 0/0 | 2805 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0028 | 0/0 | 2802 | 2 | 1 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0029 | 0/0 | 2802 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0030 | 0/0 | 2803 | 2 | 0 | 1 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0031 | 0/0 | 2800 | 2 | 0 | 0 | 1 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0032 | 0/0 | 2803 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0033 | 0/0 | 2790 | 2 | 0 | 0 | 1 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0034 | 0/0 | 2804 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0035 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0036 | 0/0 | 2815 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0037 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0038 | 0/0 | 2798 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0039 | 0/0 | 2798 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0040 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0041 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0042 | 0/0 | 2800 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0043 | 0/0 | 2803 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0044 | 0/0 | 2804 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0045 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0046 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0047 | 1/0 | 2802 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0048 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0049 | 0/0 | 2794 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0050 | 0/0 | 2800 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0051 | 0/0 | 2786 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0052 | 0/0 | 2803 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0053 | 0/0 | 2799 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0054 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0055 | 0/0 | 2800 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0056 | 0/0 | 2801 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0057 | 0/0 | 2804 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0058 | 0/0 | 2801 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0059 | 0/0 | 2803 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0060 | 0/0 | 2804 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0061 | 0/0 | 2789 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0062 | 0/0 | 2791 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0063 | 0/0 | 2803 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0064 | 0/0 | 2803 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0065 | 0/0 | 2797 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0066 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0067 | 0/0 | 2805 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0068 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0069 | 0/0 | 2794 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0070 | 0/0 | 2802 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0071 | 0/0 | 2788 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0072 | 0/0 | 2790 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0073 | 0/0 | 2791 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0074 | 0/0 | 2789 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| t0075 | 0/0 | 2803 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| 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 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| 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 | 816 | 305 | 67 | 63 | 120 | 15 | 38 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0002 | 0/0 | 816 | 6 | 5 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0003 | 0/0 | 816 | 4 | 4 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0006 | 0/0 | 816 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0007 | 0/0 | 816 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0002c0005 | 0/0 | 816 | 2 | 0 | 0 | 1 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0003c0004 | 0/0 | 816 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0004c0008 | 0/0 | 816 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0005c0009 | 0/0 | 816 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3613 | 64 | 12 | 14 | 25 | 5 | 7 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0002 | 0/0 | 3613 | 34 | 2 | 6 | 24 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0003 | 0/0 | 3618 | 32 | 0 | 2 | 28 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0004 | 0/0 | 3617 | 30 | 3 | 12 | 0 | 6 | 9 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0005 | 0/0 | 3614 | 17 | 15 | 2 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0006 | 0/0 | 3604 | 13 | 0 | 4 | 6 | 0 | 3 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0007 | 0/0 | 3614 | 8 | 2 | 1 | 1 | 2 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0008 | 0/0 | 3615 | 7 | 5 | 1 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0009 | 0/0 | 3614 | 5 | 1 | 0 | 4 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0010 | 0/0 | 3618 | 4 | 0 | 0 | 4 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0012 | 0/0 | 3608 | 4 | 4 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0013 | 0/0 | 3608 | 4 | 0 | 3 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0014 | 0/0 | 3603 | 4 | 0 | 0 | 1 | 0 | 3 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0015 | 0/0 | 3619 | 4 | 0 | 2 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0016 | 0/0 | 3612 | 3 | 0 | 2 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0017 | 0/0 | 3617 | 3 | 1 | 0 | 0 | 1 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0018 | 0/0 | 3615 | 3 | 1 | 2 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0020 | 0/0 | 3617 | 3 | 3 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0021 | 0/0 | 3618 | 3 | 0 | 1 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0022 | 0/0 | 3613 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0023 | 0/0 | 3612 | 2 | 0 | 0 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0024 | 0/0 | 3614 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0026 | 0/0 | 3613 | 2 | 1 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0027 | 0/0 | 3620 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0028 | 0/0 | 3617 | 2 | 1 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0029 | 0/0 | 3617 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0030 | 0/0 | 3618 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0031 | 0/0 | 3615 | 2 | 0 | 0 | 1 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0032 | 0/0 | 3618 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0033 | 0/0 | 3605 | 2 | 0 | 0 | 1 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0034 | 0/0 | 3619 | 2 | 0 | 0 | 2 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0036 | 0/0 | 3630 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0037 | 0/0 | 3632 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0038 | 0/0 | 3613 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0039 | 0/0 | 3613 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0040 | 0/0 | 3614 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0041 | 0/0 | 3615 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0042 | 0/0 | 3615 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0043 | 0/0 | 3618 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0044 | 0/0 | 3619 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0046 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0047 | 1/0 | 3617 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0048 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0049 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0050 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0052 | 0/0 | 3618 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0053 | 0/0 | 3614 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0054 | 0/0 | 3615 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0055 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0056 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0057 | 0/0 | 3619 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0059 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0060 | 0/0 | 3619 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0061 | 0/0 | 3604 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0062 | 0/0 | 3606 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0063 | 0/0 | 3618 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0064 | 0/0 | 3618 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0065 | 0/0 | 3612 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0066 | 0/0 | 3613 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0067 | 0/0 | 3620 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0068 | 0/0 | 3611 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0069 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0070 | 0/0 | 3617 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0071 | 0/0 | 3603 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0072 | 0/0 | 3605 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0073 | 0/0 | 3606 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0074 | 0/0 | 3604 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0001t0075 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0002t0005 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0002t0011 | 0/0 | 3602 | 4 | 3 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0002t0051 | 0/0 | 3601 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0003t0019 | 0/0 | 3615 | 3 | 3 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0003t0058 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0006t0025 | 0/0 | 3613 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0001c0007t0030 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0002c0005t0002 | 0/0 | 3613 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0002c0005t0003 | 0/0 | 3618 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0003c0004t0035 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0003c0004t0045 | 0/0 | 3613 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0004c0008t0004 | 0/0 | 3617 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| a0005c0009t0002 | 0/0 | 3613 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | copy fasta | chr4 | 37605634 | 37691376 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0006g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0007g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0008g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0009g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0009g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0009g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0010g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0010g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0012g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0012g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0013g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0013g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0013g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0013g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0014g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0014g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0014g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0015g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0015g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0015g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0015g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0016g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0016g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0016g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0017g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0017g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0017g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0018g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0020g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0020g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0021g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0021g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0021g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0022g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0022g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0023g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0023g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0024g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0024g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0026g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0026g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0027g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0027g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0028g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0028g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0029g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0029g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0030g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0031g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0031g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0032g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0032g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0033g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0033g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0034g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0034g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0036g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0037g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0038g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0039g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0040g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0041g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0042g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0043g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0044g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0046g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0047g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0048g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0049g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0050g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0052g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0053g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0054g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0055g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0056g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0057g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0059g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0060g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0061g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0062g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0063g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0064g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0065g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0066g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0067g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0068g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0069g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0070g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0071g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0072g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0073g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0074g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0001t0075g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0011g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0011g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0002t0051g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0003t0019g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0003t0019g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0003t0019g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0003t0058g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0006t0025g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0006t0025g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0001c0007t0030g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0002c0005t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0002c0005t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0003c0004t0035g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0003c0004t0045g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0004c0008t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| a0005c0009t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0067 | g0055 | EUR | GBR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | GBR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00140 | hp1 | a0004 | c0008 | t0004 | g0265 | EUR | GBR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00323 | hp1 | a0001 | c0001 | t0007 | g0040 | EUR | FIN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0242 | EUR | FIN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00438 | hp2 | a0001 | c0001 | t0041 | g0216 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0142 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00558 | hp2 | a0001 | c0001 | t0038 | g0154 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00597 | hp1 | a0001 | c0001 | t0010 | g0138 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00642 | hp2 | a0001 | c0001 | t0021 | g0029 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0176 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | CHS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0214 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00733 | hp2 | a0001 | c0001 | t0013 | g0052 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01069 | hp1 | a0001 | c0001 | t0042 | g0211 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0231 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01070 | hp1 | a0001 | c0001 | t0068 | g0077 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01071 | hp2 | a0001 | c0001 | t0013 | g0076 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01074 | hp2 | a0001 | c0001 | t0072 | g0200 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01081 | hp2 | a0001 | c0001 | t0065 | g0145 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0191 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01106 | hp2 | a0001 | c0001 | t0030 | g0011 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0016 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01167 | hp2 | a0001 | c0001 | t0018 | g0002 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01168 | hp2 | a0001 | c0002 | t0011 | g0065 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01169 | hp1 | a0001 | c0001 | t0018 | g0002 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0229 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0032 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01243 | hp2 | a0001 | c0001 | t0015 | g0251 | AMR | PUR | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0206 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01257 | hp1 | a0001 | c0001 | t0016 | g0166 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0207 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01346 | hp2 | a0001 | c0001 | t0026 | g0173 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01358 | hp1 | a0001 | c0001 | t0057 | g0121 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01358 | hp2 | a0001 | c0001 | t0043 | g0038 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0110 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0132 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01433 | hp2 | a0001 | c0001 | t0069 | g0178 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0058 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0223 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0030 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01884 | hp2 | a0001 | c0003 | t0058 | g0292 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01928 | hp2 | a0001 | c0001 | t0015 | g0071 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01943 | hp1 | a0001 | c0001 | t0053 | g0099 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01943 | hp2 | a0001 | c0001 | t0071 | g0134 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01952 | hp2 | a0001 | c0001 | t0016 | g0100 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02027 | hp1 | a0001 | c0001 | t0031 | g0148 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02027 | hp2 | a0001 | c0001 | t0027 | g0247 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0253 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02056 | hp1 | a0001 | c0001 | t0014 | g0294 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02074 | hp1 | a0001 | c0001 | t0060 | g0070 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02074 | hp2 | a0001 | c0001 | t0016 | g0171 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0307 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02129 | hp2 | a0005 | c0009 | t0002 | g0320 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02145 | hp2 | a0001 | c0001 | t0059 | g0286 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | CDX | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CDX | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02257 | hp2 | a0001 | c0001 | t0061 | g0050 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0209 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02258 | hp2 | a0001 | c0006 | t0025 | g0023 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02273 | hp1 | a0001 | c0001 | t0013 | g0078 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0068 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02280 | hp2 | a0001 | c0002 | t0005 | g0064 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0235 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02451 | hp2 | a0001 | c0001 | t0049 | g0255 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | KHV | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02572 | hp1 | a0001 | c0001 | t0018 | g0025 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0135 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02602 | hp1 | a0001 | c0007 | t0030 | g0090 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02622 | hp2 | a0001 | c0001 | t0028 | g0012 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02647 | hp1 | a0001 | c0001 | t0066 | g0272 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02647 | hp2 | a0001 | c0001 | t0056 | g0010 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0295 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02698 | hp2 | a0001 | c0001 | t0017 | g0203 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02723 | hp2 | a0001 | c0003 | t0019 | g0250 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02735 | hp1 | a0001 | c0001 | t0014 | g0003 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0083 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02738 | hp2 | a0001 | c0001 | t0075 | g0314 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0141 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02809 | hp2 | a0001 | c0002 | t0011 | g0001 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02895 | hp1 | a0001 | c0001 | t0020 | g0027 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0074 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02922 | hp2 | a0001 | c0001 | t0020 | g0018 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02970 | hp1 | a0001 | c0001 | t0020 | g0019 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02970 | hp2 | a0003 | c0004 | t0045 | g0006 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02976 | hp1 | a0001 | c0001 | t0055 | g0026 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02976 | hp2 | a0003 | c0004 | t0035 | g0005 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0084 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03130 | hp2 | a0001 | c0001 | t0012 | g0034 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0069 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03139 | hp2 | a0001 | c0001 | t0046 | g0319 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03209 | hp1 | a0001 | c0001 | t0036 | g0293 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03225 | hp2 | a0001 | c0001 | t0050 | g0013 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03486 | hp2 | a0001 | c0006 | t0025 | g0252 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0195 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03491 | hp1 | a0001 | c0001 | t0023 | g0297 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0152 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | ESN | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0257 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03540 | hp2 | a0001 | c0002 | t0011 | g0001 | AFR | GWD | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03579 | hp1 | a0001 | c0003 | t0019 | g0277 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03579 | hp2 | a0001 | c0001 | t0037 | g0254 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0157 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0312 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0080 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0053 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03688 | hp2 | a0001 | c0001 | t0033 | g0302 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03704 | hp1 | a0001 | c0001 | t0008 | g0304 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0089 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | PJL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03831 | hp1 | a0001 | c0001 | t0031 | g0087 | SAS | BEB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03831 | hp2 | a0002 | c0005 | t0003 | g0102 | SAS | BEB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03834 | hp1 | a0001 | c0001 | t0014 | g0153 | SAS | BEB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | BEB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0301 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04199 | hp1 | a0001 | c0001 | t0021 | g0079 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04199 | hp2 | a0001 | c0001 | t0007 | g0137 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04204 | hp1 | a0001 | c0001 | t0013 | g0116 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04204 | hp2 | a0001 | c0001 | t0023 | g0095 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0123 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0094 | SAS | STU | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18522 | hp2 | a0001 | c0003 | t0019 | g0092 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18612 | hp1 | a0001 | c0001 | t0006 | g0318 | EAS | CHB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0241 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18906 | hp2 | a0001 | c0001 | t0029 | g0290 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18939 | hp1 | a0001 | c0001 | t0052 | g0264 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18939 | hp2 | a0001 | c0001 | t0028 | g0271 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18942 | hp1 | a0001 | c0001 | t0070 | g0164 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18942 | hp2 | a0001 | c0001 | t0022 | g0197 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18950 | hp1 | a0001 | c0001 | t0054 | g0263 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18954 | hp2 | a0001 | c0001 | t0009 | g0160 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18956 | hp1 | a0001 | c0001 | t0024 | g0167 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18956 | hp2 | a0001 | c0001 | t0064 | g0240 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18964 | hp1 | a0001 | c0001 | t0010 | g0149 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18967 | hp2 | a0001 | c0001 | t0015 | g0133 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18977 | hp1 | a0001 | c0001 | t0073 | g0044 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18977 | hp2 | a0001 | c0001 | t0027 | g0061 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18979 | hp1 | a0001 | c0001 | t0022 | g0120 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18983 | hp1 | a0001 | c0001 | t0010 | g0062 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18988 | hp1 | a0001 | c0001 | t0074 | g0093 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18994 | hp1 | a0001 | c0001 | t0015 | g0143 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA18995 | hp2 | a0001 | c0001 | t0032 | g0119 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19000 | hp2 | a0001 | c0001 | t0032 | g0097 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19001 | hp1 | a0001 | c0001 | t0009 | g0161 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0310 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19003 | hp2 | a0001 | c0001 | t0009 | g0174 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19009 | hp2 | a0002 | c0005 | t0002 | g0186 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19010 | hp1 | a0001 | c0001 | t0024 | g0124 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19030 | hp1 | a0001 | c0001 | t0048 | g0256 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19030 | hp2 | a0001 | c0001 | t0029 | g0114 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19043 | hp1 | a0001 | c0002 | t0011 | g0067 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19054 | hp2 | a0001 | c0001 | t0040 | g0266 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19058 | hp1 | a0001 | c0001 | t0034 | g0182 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19067 | hp1 | a0001 | c0001 | t0034 | g0147 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19067 | hp2 | a0001 | c0001 | t0009 | g0303 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19083 | hp1 | a0001 | c0001 | t0039 | g0244 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19083 | hp2 | a0001 | c0001 | t0010 | g0063 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19087 | hp1 | a0001 | c0001 | t0033 | g0218 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0258 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0028 | AFR | YRI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0047 | EUR | TSI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20752 | hp2 | a0001 | c0001 | t0017 | g0060 | EUR | TSI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0245 | EUR | TSI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0165 | EUR | TSI | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20905 | hp1 | a0001 | c0001 | t0014 | g0003 | SAS | GIH | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20905 | hp2 | a0001 | c0001 | t0021 | g0059 | SAS | GIH | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0104 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02486 | hp1 | a0001 | c0001 | t0044 | g0039 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02559 | hp1 | a0001 | c0001 | t0063 | g0289 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ACB | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0291 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG03471 | hp2 | a0001 | c0002 | t0051 | g0066 | AFR | MSL | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | USA | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| HG06807 | hp2 | a0001 | c0001 | t0017 | g0049 | AFR | USA | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20300 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | USA | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA20300 | hp2 | a0001 | c0001 | t0026 | g0280 | AFR | USA | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA21309 | hp1 | a0001 | c0001 | t0062 | g0048 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | LWK | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0128 | REF | REF | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0047 | g0288 | REF | REF | RELL1_chr4_37605634_37691376 | RELL1 | chr4 | 37605634 | 37691376 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37631404
|
C | T | 1 | a0004 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.800G>A | p.Arg267His | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/7 | 889/3617 | 800/816 | 267/271 | chr4 | 37631404 | ||
| chr4:37649441
|
C | T | 1 | a0002 | 2 | HG03831.hp2 NA19009.hp2 |
missense_variant | MODERATE | c.148G>A | p.Asp50Asn | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/7 | 237/3617 | 148/816 | 50/271 | chr4 | 37649441 | ||
| chr4:37686239
|
A | G | 1 | a0003 | 2 | HG02970.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.49T>C | p.Phe17Leu | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/7 | 138/3617 | 49/816 | 17/271 | chr4 | 37686239 | ||
| chr4:37686260
|
C | A | 1 | a0005 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.28G>T | p.Ala10Ser | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/7 | 117/3617 | 28/816 | 10/271 | chr4 | 37686260 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37631469
|
C | T | 1 | a0001c0003 | 4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.735G>A | p.Leu245Leu | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/7 | 824/3617 | 735/816 | 245/271 | chr4 | 37631469 | ||
| chr4:37635021
|
C | T | 1 | a0001c0006 | 2 | HG02258.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.546G>A | p.Thr182Thr | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/7 | 635/3617 | 546/816 | 182/271 | chr4 | 37635021 | ||
| chr4:37638458
|
A | G | 1 | a0001c0002 | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
synonymous_variant | LOW | c.432T>C | p.Tyr144Tyr | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/7 | 521/3617 | 432/816 | 144/271 | chr4 | 37638458 | ||
| chr4:37638497
|
A | G | 1 | a0001c0007 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.393T>C | p.Ala131Ala | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/7 | 482/3617 | 393/816 | 131/271 | chr4 | 37638497 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37610728
|
T | C | 1 | a0001c0001t0042 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2618A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20660 | chr4 | 37610728 | |||||
| chr4:37610864
|
T | A | 77 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(74): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*2482A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20524 | chr4 | 37610864 | |||||
| chr4:37610897
|
G | A | 3 | a0001c0001t0017a0001c0001t0043a0001c0001t0044 | 5 | HG01358.hp2 HG02486.hp1 HG02698.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2449C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20491 | chr4 | 37610897 | |||||
| chr4:37610904
|
G | A | 10 | a0001c0001t0004a0001c0001t0017a0001c0001t0020others(7): Show | 43 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2442C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20484 | chr4 | 37610904 | |||||
| chr4:37610945
|
G | A | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2401C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20443 | chr4 | 37610945 | |||||
| chr4:37610947
|
A | G | 6 | a0001c0001t0006a0001c0001t0033a0001c0001t0039others(3): Show | 19 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2399T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20441 | chr4 | 37610947 | |||||
| chr4:37611008
|
G | A | 1 | a0001c0001t0053 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2338C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20380 | chr4 | 37611008 | |||||
| chr4:37611110
|
A | AAAG | 18 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(15): Show | 64 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2233_*2235dupCTT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20277 | chr4 | 37611110 | |||||
| chr4:37611312
|
T | G | 1 | a0001c0001t0014 | 4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2034A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20076 | chr4 | 37611312 | |||||
| chr4:37611379
|
AGT | A | 2 | a0001c0002t0011a0001c0002t0051 | 5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1965_*1966delAC | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 20007 | chr4 | 37611379 | |||||
| chr4:37611630
|
T | C | 1 | a0001c0001t0062 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1716A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19758 | chr4 | 37611630 | |||||
| chr4:37611834
|
A | G | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1512T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19554 | chr4 | 37611834 | |||||
| chr4:37611854
|
G | C | 1 | a0001c0001t0042 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1492C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19534 | chr4 | 37611854 | |||||
| chr4:37611902
|
G | A | 1 | a0001c0001t0012 | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1444C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19486 | chr4 | 37611902 | |||||
| chr4:37611933
|
T | C | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1413A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19455 | chr4 | 37611933 | |||||
| chr4:37611960
|
G | C | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1386C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19428 | chr4 | 37611960 | |||||
| chr4:37611992
|
G | A | 13 | a0001c0001t0012a0001c0001t0013a0001c0001t0021others(10): Show | 24 | HG00642.hp2 HG00733.hp2 HG01070.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1354C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19396 | chr4 | 37611992 | |||||
| chr4:37612003
|
G | T | 1 | a0001c0001t0038 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1343C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19385 | chr4 | 37612003 | |||||
| chr4:37612176
|
CA | C | 18 | a0001c0001t0010a0001c0001t0024a0001c0001t0031others(15): Show | 24 | HG00438.hp2 HG00597.hp1 HG01074.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1169delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19211 | chr4 | 37612176 | |||||
| chr4:37612176
|
CAA | C | 43 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*1168_*1169delTT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19210 | chr4 | 37612176 | |||||
| chr4:37612176
|
CAAA | C | 8 | a0001c0001t0012a0001c0001t0013a0001c0001t0016others(5): Show | 17 | HG00733.hp2 HG01071.hp2 HG01081.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1167_*1169delTTT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19209 | chr4 | 37612176 | |||||
| chr4:37612275
|
T | A | 2 | a0001c0001t0048a0001c0006t0025 | 3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1071A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19113 | chr4 | 37612275 | |||||
| chr4:37612308
|
G | A | 10 | a0001c0001t0004a0001c0001t0017a0001c0001t0020others(7): Show | 43 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1038C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19080 | chr4 | 37612308 | |||||
| chr4:37612322
|
T | TTA | 16 | a0001c0001t0004a0001c0001t0010a0001c0001t0017others(13): Show | 53 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1024insTA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19065 | chr4 | 37612322 | |||||
| chr4:37612322
|
T | TTAA | 2 | a0001c0001t0027a0001c0001t0032 | 4 | HG02027.hp2 NA18977.hp2 NA18995.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1023_*1024insTTA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19065 | chr4 | 37612322 | |||||
| chr4:37612322
|
TAA | T | 6 | a0001c0001t0018a0001c0001t0046a0001c0003t0019others(3): Show | 10 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1022_*1023delTT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19064 | chr4 | 37612322 | |||||
| chr4:37612324
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0074 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1007_*1021delGTTT others(11): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612324 | |||||
| chr4:37612327
|
AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0014 | 4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1018delGTTT others(8): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612327 | |||||
| chr4:37612328
|
AAAAAAAA others(4): Show |
A | 5 | a0001c0001t0006a0001c0001t0033a0001c0001t0071others(2): Show | 18 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1017delGTTT others(7): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612328 | |||||
| chr4:37612330
|
AAAAAAAA others(2): Show |
A | 5 | a0001c0001t0012a0001c0001t0013a0001c0001t0049others(2): Show | 11 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1015delGTTT others(5): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612330 | |||||
| chr4:37612333
|
A | C | 1 | a0001c0001t0022 | 2 | NA18942.hp2 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1013T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19055 | chr4 | 37612333 | |||||
| chr4:37612334
|
A | C | 5 | a0001c0001t0003a0001c0001t0015a0001c0001t0021others(2): Show | 42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1012T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19054 | chr4 | 37612334 | |||||
| chr4:37612334
|
AAAAACAA others(8): Show |
A | 4 | a0001c0001t0061a0001c0001t0062a0001c0002t0011others(1): Show | 7 | HG01168.hp2 HG02257.hp2 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*997_*1011delGTTTT others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19039 | chr4 | 37612334 | |||||
| chr4:37612336
|
A | C | 9 | a0001c0001t0001a0001c0001t0007a0001c0001t0023others(6): Show | 83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1010T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19052 | chr4 | 37612336 | |||||
| chr4:37612337
|
AAC | A | 21 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(18): Show | 136 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*1007_*1008delGT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612337 | |||||
| chr4:37612338
|
AC | A | 6 | a0001c0001t0005a0001c0001t0029a0001c0001t0041others(3): Show | 23 | HG00438.hp2 HG01243.hp1 HG01255.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1007delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612338 | |||||
| chr4:37612339
|
C | A | 28 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(25): Show | 110 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1007G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19049 | chr4 | 37612339 | |||||
| chr4:37612340
|
A | C | 9 | a0001c0001t0004a0001c0001t0017a0001c0001t0030others(6): Show | 40 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1006T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19048 | chr4 | 37612340 | |||||
| chr4:37612342
|
A | C | 18 | a0001c0001t0002a0001c0001t0005a0001c0001t0009others(15): Show | 75 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1004T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19046 | chr4 | 37612342 | |||||
| chr4:37612349
|
C | A | 10 | a0001c0001t0013a0001c0001t0028a0001c0001t0032others(7): Show | 15 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*997G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 19039 | chr4 | 37612349 | |||||
| chr4:37612402
|
G | A | 9 | a0001c0001t0003a0001c0001t0015a0001c0001t0021others(6): Show | 47 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*944C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18986 | chr4 | 37612402 | |||||
| chr4:37612416
|
G | A | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*930C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18972 | chr4 | 37612416 | |||||
| chr4:37612590
|
T | G | 1 | a0001c0001t0052 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*756A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18798 | chr4 | 37612590 | |||||
| chr4:37612624
|
G | A | 7 | a0001c0001t0003a0001c0001t0015a0001c0001t0021others(4): Show | 44 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*722C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18764 | chr4 | 37612624 | |||||
| chr4:37612624
|
G | T | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*722C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18764 | chr4 | 37612624 | |||||
| chr4:37612636
|
C | CA | 23 | a0001c0001t0007a0001c0001t0009a0001c0001t0015others(20): Show | 43 | HG00323.hp1 HG01106.hp2 HG01168.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*709dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18751 | chr4 | 37612636 | |||||
| chr4:37612636
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0036 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*697_*709dupTTTTTT others(7): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18751 | chr4 | 37612636 | |||||
| chr4:37612636
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0037 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*695_*709dupTTTTTT others(9): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18751 | chr4 | 37612636 | |||||
| chr4:37612656
|
C | A | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18732 | chr4 | 37612656 | |||||
| chr4:37612657
|
C | A | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*689G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18731 | chr4 | 37612657 | |||||
| chr4:37612658
|
T | A | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*688A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18730 | chr4 | 37612658 | |||||
| chr4:37612659
|
T | C | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*687A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18729 | chr4 | 37612659 | |||||
| chr4:37612697
|
T | C | 13 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(10): Show | 56 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*649A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18691 | chr4 | 37612697 | |||||
| chr4:37612721
|
T | C | 1 | a0001c0001t0066 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18667 | chr4 | 37612721 | |||||
| chr4:37612781
|
T | A | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*565A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18607 | chr4 | 37612781 | |||||
| chr4:37612782
|
C | T | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*564G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18606 | chr4 | 37612782 | |||||
| chr4:37612938
|
G | A | 4 | a0001c0001t0013a0001c0001t0067a0001c0001t0068others(1): Show | 7 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*408C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18450 | chr4 | 37612938 | |||||
| chr4:37612949
|
C | T | 2 | a0001c0001t0036a0001c0001t0037 | 2 | HG03209.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*397G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18439 | chr4 | 37612949 | |||||
| chr4:37612967
|
C | A | 2 | a0001c0001t0032a0001c0001t0070 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*379G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18421 | chr4 | 37612967 | |||||
| chr4:37613115
|
C | A | 13 | a0001c0001t0003a0001c0001t0006a0001c0001t0014others(10): Show | 66 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 7/7 | 18273 | chr4 | 37613115 | |||||
| chr4:37686343
|
C | G | 1 | a0003c0004t0035 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/7 | 56 | chr4 | 37686343 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:37613429
|
G | T | 6 | a0001c0001t0008g0008a0001c0001t0008g0016a0001c0001t0008g0022others(3): Show | 6 | HG01167.hp1 HG02258.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.*4-87C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613429 | ||||||
| chr4:37613442
|
C | G | 1 | a0001c0001t0002g0127 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.*4-100G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613442 | ||||||
| chr4:37613513
|
G | T | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-171C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613513 | ||||||
| chr4:37613577
|
T | C | 318 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(315): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.*4-235A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613577 | ||||||
| chr4:37613611
|
C | T | 2 | a0001c0001t0004g0080a0001c0001t0004g0089 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-269G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613611 | ||||||
| chr4:37613642
|
G | A | 3 | a0001c0001t0028g0012a0001c0001t0028g0271a0001c0001t0064g0240 | 3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*4-300C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613642 | ||||||
| chr4:37613668
|
C | G | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-326G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613668 | ||||||
| chr4:37613701
|
A | G | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-359T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613701 | ||||||
| chr4:37613829
|
G | A | 1 | a0001c0001t0003g0113 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.*4-487C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613829 | ||||||
| chr4:37613952
|
C | G | 229 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(226): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.*4-610G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613952 | ||||||
| chr4:37613989
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(50): Show | 54 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.*4-647C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37613989 | ||||||
| chr4:37614057
|
C | T | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-715G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614057 | ||||||
| chr4:37614069
|
A | G | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-727T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614069 | ||||||
| chr4:37614086
|
A | G | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.*4-744T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614086 | ||||||
| chr4:37614108
|
C | T | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-766G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614108 | ||||||
| chr4:37614112
|
G | A | 3 | a0001c0001t0028g0012a0001c0001t0028g0271a0001c0001t0064g0240 | 3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*4-770C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614112 | ||||||
| chr4:37614202
|
T | C | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-860A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614202 | ||||||
| chr4:37614294
|
A | G | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-952T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614294 | ||||||
| chr4:37614298
|
T | C | 44 | a0001c0001t0003g0051a0001c0001t0003g0072a0001c0001t0003g0094others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.*4-956A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614298 | ||||||
| chr4:37614474
|
C | A | 1 | a0001c0001t0021g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.*4-1132G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614474 | ||||||
| chr4:37614484
|
A | G | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-1142T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614484 | ||||||
| chr4:37614670
|
C | T | 17 | a0001c0001t0012g0034a0001c0001t0012g0135a0001c0001t0012g0141others(14): Show | 18 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.*4-1328G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614670 | ||||||
| chr4:37614756
|
A | G | 2 | a0001c0001t0004g0080a0001c0001t0004g0089 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.*4-1414T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614756 | ||||||
| chr4:37614764
|
G | A | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*4-1422C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614764 | ||||||
| chr4:37614952
|
T | G | 4 | a0001c0001t0020g0018a0001c0001t0020g0019a0001c0001t0020g0027others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-1610A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37614952 | ||||||
| chr4:37615007
|
G | A | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.*4-1665C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615007 | ||||||
| chr4:37615070
|
G | C | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.*4-1728C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615070 | ||||||
| chr4:37615217
|
T | C | 4 | a0001c0001t0002g0194a0001c0001t0002g0261a0001c0001t0002g0315others(1): Show | 4 | HG02129.hp2 NA18988.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-1875A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615217 | ||||||
| chr4:37615353
|
C | T | 46 | a0001c0001t0004g0030a0001c0001t0004g0047a0001c0001t0004g0053others(43): Show | 46 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.*4-2011G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615353 | ||||||
| chr4:37615367
|
A | G | 6 | a0001c0001t0001g0117a0001c0001t0001g0215a0001c0001t0001g0219others(3): Show | 6 | HG01256.hp1 HG01257.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-2025T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615367 | ||||||
| chr4:37615767
|
A | G | 80 | a0001c0001t0001g0298a0001c0001t0002g0009a0001c0001t0002g0042others(77): Show | 80 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.*4-2425T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615767 | ||||||
| chr4:37615796
|
G | T | 1 | a0001c0002t0011g0065 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.*4-2454C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615796 | ||||||
| chr4:37615827
|
T | C | 4 | a0001c0002t0011g0001a0001c0002t0011g0065a0001c0002t0011g0067others(1): Show | 5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-2485A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615827 | ||||||
| chr4:37615957
|
C | T | 4 | a0001c0001t0013g0052a0001c0001t0013g0076a0001c0001t0068g0077others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-2615G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37615957 | ||||||
| chr4:37616023
|
T | TAAGAAAC others(332): Show |
1 | a0001c0001t0002g0187 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*4-2682_*4-2681ins others(339): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616023 | ||||||
| chr4:37616069
|
A | G | 1 | a0001c0001t0031g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*4-2727T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616069 | ||||||
| chr4:37616157
|
G | T | 4 | a0001c0002t0011g0001a0001c0002t0011g0065a0001c0002t0011g0067others(1): Show | 5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-2815C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616157 | ||||||
| chr4:37616158
|
GTAC | G | 4 | a0001c0002t0011g0001a0001c0002t0011g0065a0001c0002t0011g0067others(1): Show | 5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-2819_*4-2817del others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616158 | ||||||
| chr4:37616486
|
G | A | 4 | a0001c0002t0011g0001a0001c0002t0011g0065a0001c0002t0011g0067others(1): Show | 5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*4-3144C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616486 | ||||||
| chr4:37616646
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.*4-3304G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616646 | ||||||
| chr4:37616678
|
AAAAT | A | 77 | a0001c0001t0002g0009a0001c0001t0002g0042a0001c0001t0002g0045others(74): Show | 77 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.*4-3340_*4-3337del others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616678 | ||||||
| chr4:37616693
|
C | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-3351G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616693 | ||||||
| chr4:37616888
|
G | A | 1 | a0001c0001t0043g0038 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.*4-3546C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37616888 | ||||||
| chr4:37617227
|
C | T | 2 | a0001c0001t0046g0319a0003c0004t0035g0005 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.*4-3885G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617227 | ||||||
| chr4:37617280
|
T | C | 4 | a0001c0001t0008g0304a0001c0001t0028g0012a0001c0001t0028g0271others(1): Show | 4 | HG02622.hp2 HG03704.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-3938A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617280 | ||||||
| chr4:37617285
|
G | A | 3 | a0001c0001t0048g0256a0001c0006t0025g0023a0001c0006t0025g0252 | 3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*4-3943C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617285 | ||||||
| chr4:37617302
|
T | C | 2 | a0001c0001t0018g0002a0001c0001t0018g0025 | 3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.*4-3960A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617302 | ||||||
| chr4:37617316
|
A | G | 89 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(86): Show | 90 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.*4-3974T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617316 | ||||||
| chr4:37617361
|
C | T | 1 | a0001c0001t0026g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*4-4019G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617361 | ||||||
| chr4:37617801
|
A | T | 1 | a0001c0001t0009g0028 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.*4-4459T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617801 | ||||||
| chr4:37617873
|
T | G | 4 | a0001c0001t0008g0304a0001c0001t0028g0012a0001c0001t0028g0271others(1): Show | 4 | HG02622.hp2 HG03704.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-4531A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37617873 | ||||||
| chr4:37618170
|
G | A | 1 | a0001c0001t0003g0168 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.*4-4828C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618170 | ||||||
| chr4:37618171
|
T | G | 4 | a0001c0001t0012g0034a0001c0001t0012g0135a0001c0001t0012g0141others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-4829A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618171 | ||||||
| chr4:37618399
|
T | A | 28 | a0001c0001t0006g0104a0001c0001t0006g0142a0001c0001t0006g0152others(25): Show | 29 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.*4-5057A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618399 | ||||||
| chr4:37618494
|
T | A | 1 | a0001c0001t0004g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.*4-5152A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618494 | ||||||
| chr4:37618529
|
C | A | 1 | a0001c0001t0030g0011 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*4-5187G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618529 | ||||||
| chr4:37618547
|
A | G | 22 | a0001c0001t0006g0104a0001c0001t0006g0142a0001c0001t0006g0152others(19): Show | 23 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.*4-5205T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618547 | ||||||
| chr4:37618595
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.*4-5253A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618595 | ||||||
| chr4:37618832
|
T | C | 7 | a0001c0001t0010g0062a0001c0001t0010g0063a0001c0001t0010g0149others(4): Show | 7 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.*4-5490A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618832 | ||||||
| chr4:37618866
|
G | A | 4 | a0001c0001t0008g0304a0001c0001t0028g0012a0001c0001t0028g0271others(1): Show | 4 | HG02622.hp2 HG03704.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-5524C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618866 | ||||||
| chr4:37618867
|
T | TTTTTC | 60 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(57): Show | 61 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.*4-5530_*4-5526dup others(5): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618867 | ||||||
| chr4:37618867
|
T | TTTTTCTT others(3): Show |
10 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0268others(7): Show | 10 | HG01175.hp2 HG02027.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.*4-5535_*4-5526dup others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37618867 | ||||||
| chr4:37619042
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.*4-5700C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619042 | ||||||
| chr4:37619186
|
C | G | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.*4-5844G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619186 | ||||||
| chr4:37619322
|
A | G | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-5980T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619322 | ||||||
| chr4:37619342
|
C | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0107a0001c0001t0001g0192others(3): Show | 6 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.*4-6000G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619342 | ||||||
| chr4:37619430
|
G | T | 233 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(230): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.*4-6088C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619430 | ||||||
| chr4:37619470
|
C | T | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.*4-6128G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619470 | ||||||
| chr4:37619596
|
C | T | 18 | a0001c0001t0002g0096a0001c0001t0002g0103a0001c0001t0002g0118others(15): Show | 18 | HG00423.hp2 HG01106.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.*4-6254G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619596 | ||||||
| chr4:37619652
|
C | T | 1 | a0002c0005t0002g0186 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.*4-6310G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37619652 | ||||||
| chr4:37620268
|
C | T | 1 | a0001c0001t0009g0303 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.*4-6926G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37620268 | ||||||
| chr4:37620547
|
C | A | 1 | a0001c0001t0014g0294 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.*4-7205G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37620547 | ||||||
| chr4:37620943
|
C | T | 3 | a0001c0001t0028g0012a0001c0001t0028g0271a0001c0001t0064g0240 | 3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*4-7601G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37620943 | ||||||
| chr4:37620963
|
G | C | 1 | a0001c0001t0046g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*4-7621C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37620963 | ||||||
| chr4:37621138
|
A | G | 51 | a0001c0001t0003g0051a0001c0001t0003g0072a0001c0001t0003g0094others(48): Show | 51 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.*4-7796T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621138 | ||||||
| chr4:37621300
|
C | CA | 4 | a0001c0003t0019g0092a0001c0003t0019g0250a0001c0003t0019g0277others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*4-7959dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621300 | ||||||
| chr4:37621330
|
C | A | 3 | a0001c0001t0048g0256a0001c0006t0025g0023a0001c0006t0025g0252 | 3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*4-7988G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621330 | ||||||
| chr4:37621348
|
C | T | 41 | a0001c0001t0003g0051a0001c0001t0003g0072a0001c0001t0003g0094others(38): Show | 41 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.*4-8006G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621348 | ||||||
| chr4:37621563
|
G | A | 3 | a0001c0001t0028g0012a0001c0001t0028g0271a0001c0001t0064g0240 | 3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*4-8221C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621563 | ||||||
| chr4:37621702
|
A | T | 27 | a0001c0001t0006g0104a0001c0001t0006g0142a0001c0001t0006g0152others(24): Show | 28 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.*4-8360T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621702 | ||||||
| chr4:37621811
|
G | C | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8469C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621811 | ||||||
| chr4:37621851
|
A | C | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8509T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621851 | ||||||
| chr4:37621880
|
A | G | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8538T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621880 | ||||||
| chr4:37621948
|
A | C | 4 | a0001c0001t0017g0049a0001c0001t0017g0203a0001c0001t0043g0038others(1): Show | 4 | HG01358.hp2 HG02486.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.*4-8606T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37621948 | ||||||
| chr4:37622074
|
A | G | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8732T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622074 | ||||||
| chr4:37622167
|
G | T | 1 | a0001c0001t0022g0197 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.*4-8825C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622167 | ||||||
| chr4:37622215
|
T | C | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*4-8873A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622215 | ||||||
| chr4:37622583
|
G | A | 1 | a0001c0001t0037g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.*3+8802C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622583 | ||||||
| chr4:37622696
|
G | A | 1 | a0001c0001t0005g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.*3+8689C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622696 | ||||||
| chr4:37622749
|
A | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+8636T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622749 | ||||||
| chr4:37622797
|
T | C | 1 | a0001c0001t0005g0021 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.*3+8588A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622797 | ||||||
| chr4:37622799
|
C | CT | 12 | a0001c0001t0001g0146a0001c0001t0003g0212a0001c0001t0004g0053others(9): Show | 12 | HG01175.hp2 HG02027.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.*3+8585dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622799 | ||||||
| chr4:37622799
|
C | T | 26 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(23): Show | 26 | HG00642.hp1 HG01175.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.*3+8586G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622799 | ||||||
| chr4:37622819
|
T | C | 2 | a0001c0001t0018g0002a0001c0001t0018g0025 | 3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.*3+8566A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37622819 | ||||||
| chr4:37623005
|
G | A | 3 | a0001c0001t0003g0122a0001c0001t0034g0147a0001c0001t0074g0093 | 3 | HG02071.hp2 NA18988.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.*3+8380C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623005 | ||||||
| chr4:37623095
|
A | G | 316 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(313): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.*3+8290T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623095 | ||||||
| chr4:37623099
|
G | A | 4 | a0001c0002t0011g0001a0001c0002t0011g0065a0001c0002t0011g0067others(1): Show | 5 | HG01168.hp2 HG02809.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.*3+8286C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623099 | ||||||
| chr4:37623137
|
A | C | 3 | a0001c0001t0048g0256a0001c0006t0025g0023a0001c0006t0025g0252 | 3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+8248T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623137 | ||||||
| chr4:37623582
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.*3+7803G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623582 | ||||||
| chr4:37623617
|
G | A | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+7768C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623617 | ||||||
| chr4:37623649
|
C | G | 4 | a0001c0003t0019g0092a0001c0003t0019g0250a0001c0003t0019g0277others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+7736G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623649 | ||||||
| chr4:37623671
|
A | C | 4 | a0001c0003t0019g0092a0001c0003t0019g0250a0001c0003t0019g0277others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+7714T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623671 | ||||||
| chr4:37623710
|
G | A | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+7675C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623710 | ||||||
| chr4:37623829
|
G | A | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+7556C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623829 | ||||||
| chr4:37623953
|
A | T | 7 | a0001c0001t0002g0096a0001c0001t0002g0159a0001c0001t0002g0162others(4): Show | 7 | HG02080.hp1 NA18946.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.*3+7432T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37623953 | ||||||
| chr4:37624035
|
G | A | 1 | a0001c0001t0062g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*3+7350C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624035 | ||||||
| chr4:37624048
|
G | T | 3 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291 | 3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.*3+7337C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624048 | ||||||
| chr4:37624050
|
C | A | 2 | a0001c0001t0001g0311a0001c0001t0007g0310 | 2 | NA18969.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.*3+7335G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624050 | ||||||
| chr4:37624078
|
CCA | C | 2 | a0001c0001t0014g0003a0001c0001t0014g0153 | 3 | HG02735.hp1 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.*3+7305_*3+7306del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624078 | ||||||
| chr4:37624184
|
T | C | 1 | a0001c0001t0039g0244 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.*3+7201A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624184 | ||||||
| chr4:37624252
|
G | A | 10 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291others(7): Show | 10 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.*3+7133C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624252 | ||||||
| chr4:37624393
|
G | A | 7 | a0001c0001t0008g0008a0001c0001t0008g0016a0001c0001t0008g0022others(4): Show | 7 | HG01167.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.*3+6992C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624393 | ||||||
| chr4:37624418
|
C | CT | 25 | a0001c0001t0001g0260a0001c0001t0006g0104a0001c0001t0006g0142others(22): Show | 26 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.*3+6966dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624418 | ||||||
| chr4:37624418
|
C | T | 3 | a0001c0001t0048g0256a0001c0006t0025g0023a0001c0006t0025g0252 | 3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+6967G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624418 | ||||||
| chr4:37624418
|
CT | C | 193 | a0001c0001t0001g0024a0001c0001t0001g0111a0001c0001t0001g0125others(190): Show | 195 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.*3+6966delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624418 | ||||||
| chr4:37624418
|
CTT | C | 52 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.*3+6965_*3+6966del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624418 | ||||||
| chr4:37624422
|
T | C | 10 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291others(7): Show | 10 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.*3+6963A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624422 | ||||||
| chr4:37624573
|
G | A | 2 | a0001c0001t0029g0114a0001c0001t0029g0290 | 2 | NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.*3+6812C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624573 | ||||||
| chr4:37624580
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.*3+6805G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624580 | ||||||
| chr4:37624614
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0001g0185 | 2 | NA18945.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.*3+6771T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624614 | ||||||
| chr4:37624620
|
G | A | 3 | a0001c0001t0048g0256a0001c0006t0025g0023a0001c0006t0025g0252 | 3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+6765C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624620 | ||||||
| chr4:37624849
|
T | G | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+6536A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624849 | ||||||
| chr4:37624952
|
G | A | 1 | a0001c0001t0046g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*3+6433C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37624952 | ||||||
| chr4:37625003
|
G | A | 4 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0075others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.*3+6382C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625003 | ||||||
| chr4:37625142
|
C | T | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*3+6243G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625142 | ||||||
| chr4:37625231
|
T | G | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+6154A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625231 | ||||||
| chr4:37625308
|
G | GGACAATG others(339): Show |
1 | a0001c0001t0005g0224 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.*3+6076_*3+6077ins others(346): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625308 | ||||||
| chr4:37625366
|
A | T | 1 | a0001c0001t0062g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.*3+6019T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625366 | ||||||
| chr4:37625673
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.*3+5712C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625673 | ||||||
| chr4:37625717
|
A | C | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+5668T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625717 | ||||||
| chr4:37625909
|
T | TA | 52 | a0001c0001t0003g0051a0001c0001t0003g0072a0001c0001t0003g0094others(49): Show | 52 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.*3+5475dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625909 | ||||||
| chr4:37625973
|
C | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+5412G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37625973 | ||||||
| chr4:37626048
|
A | G | 7 | a0001c0001t0010g0062a0001c0001t0010g0063a0001c0001t0010g0149others(4): Show | 7 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.*3+5337T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626048 | ||||||
| chr4:37626370
|
C | T | 5 | a0001c0001t0017g0049a0001c0001t0017g0060a0001c0001t0017g0203others(2): Show | 5 | HG01358.hp2 HG02486.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.*3+5015G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626370 | ||||||
| chr4:37626548
|
G | C | 11 | a0001c0001t0004g0030a0001c0001t0004g0080a0001c0001t0004g0083others(8): Show | 11 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.*3+4837C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626548 | ||||||
| chr4:37626614
|
T | C | 1 | a0001c0001t0004g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.*3+4771A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626614 | ||||||
| chr4:37626698
|
G | A | 3 | a0001c0001t0021g0029a0001c0001t0021g0059a0001c0001t0021g0079 | 3 | HG00642.hp2 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.*3+4687C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626698 | ||||||
| chr4:37626802
|
G | A | 88 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.*3+4583C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626802 | ||||||
| chr4:37626827
|
A | G | 1 | a0001c0001t0003g0181 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.*3+4558T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626827 | ||||||
| chr4:37626863
|
G | C | 1 | a0001c0001t0018g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.*3+4522C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626863 | ||||||
| chr4:37626937
|
C | G | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+4448G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626937 | ||||||
| chr4:37626999
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*3+4386A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37626999 | ||||||
| chr4:37627101
|
C | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+4284G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627101 | ||||||
| chr4:37627377
|
A | G | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+4008T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627377 | ||||||
| chr4:37627433
|
A | G | 2 | a0001c0001t0018g0002a0001c0001t0018g0025 | 3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.*3+3952T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627433 | ||||||
| chr4:37627441
|
C | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+3944G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627441 | ||||||
| chr4:37627659
|
T | C | 18 | a0001c0001t0006g0104a0001c0001t0006g0142a0001c0001t0006g0152others(15): Show | 18 | HG00544.hp2 HG00673.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.*3+3726A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627659 | ||||||
| chr4:37627722
|
A | G | 1 | a0001c0001t0046g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*3+3663T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37627722 | ||||||
| chr4:37628044
|
T | C | 4 | a0001c0001t0001g0311a0001c0001t0003g0259a0001c0001t0003g0262others(1): Show | 4 | HG00597.hp2 NA18969.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.*3+3341A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628044 | ||||||
| chr4:37628152
|
A | G | 1 | a0001c0001t0031g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*3+3233T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628152 | ||||||
| chr4:37628208
|
T | G | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+3177A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628208 | ||||||
| chr4:37628353
|
G | T | 2 | a0001c0003t0019g0092a0001c0003t0019g0277 | 2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.*3+3032C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628353 | ||||||
| chr4:37628381
|
C | T | 3 | a0001c0001t0048g0256a0001c0006t0025g0023a0001c0006t0025g0252 | 3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+3004G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628381 | ||||||
| chr4:37628418
|
C | T | 9 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291others(6): Show | 9 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.*3+2967G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628418 | ||||||
| chr4:37628516
|
T | C | 4 | a0001c0001t0020g0018a0001c0001t0020g0019a0001c0001t0020g0027others(1): Show | 4 | HG02895.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+2869A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628516 | ||||||
| chr4:37628673
|
C | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*3+2712G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628673 | ||||||
| chr4:37628789
|
G | A | 9 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291others(6): Show | 9 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.*3+2596C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628789 | ||||||
| chr4:37628830
|
C | T | 4 | a0001c0003t0019g0092a0001c0003t0019g0250a0001c0003t0019g0277others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+2555G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628830 | ||||||
| chr4:37628953
|
C | T | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.*3+2432G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628953 | ||||||
| chr4:37628954
|
G | A | 1 | a0001c0001t0017g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*3+2431C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37628954 | ||||||
| chr4:37629680
|
GCTAA | G | 3 | a0001c0001t0028g0012a0001c0001t0028g0271a0001c0001t0064g0240 | 3 | HG02622.hp2 NA18939.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.*3+1701_*3+1704del others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629680 | ||||||
| chr4:37629784
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.*3+1601C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629784 | ||||||
| chr4:37629901
|
C | T | 6 | a0001c0001t0013g0052a0001c0001t0013g0076a0001c0001t0013g0078others(3): Show | 6 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.*3+1484G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629901 | ||||||
| chr4:37629954
|
C | G | 4 | a0001c0001t0008g0304a0001c0001t0014g0003a0001c0001t0014g0153others(1): Show | 5 | HG02056.hp1 HG02735.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.*3+1431G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629954 | ||||||
| chr4:37629972
|
A | G | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.*3+1413T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37629972 | ||||||
| chr4:37630252
|
A | C | 20 | a0001c0001t0004g0047a0001c0001t0004g0053a0001c0001t0004g0054others(17): Show | 20 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.*3+1133T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630252 | ||||||
| chr4:37630279
|
G | A | 6 | a0001c0001t0013g0052a0001c0001t0013g0076a0001c0001t0013g0078others(3): Show | 6 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.*3+1106C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630279 | ||||||
| chr4:37630356
|
G | GT | 103 | a0001c0001t0001g0117a0001c0001t0001g0172a0001c0001t0001g0215others(100): Show | 105 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.*3+1028dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | ||||||
| chr4:37630356
|
G | GTT | 38 | a0001c0001t0001g0015a0001c0001t0001g0033a0001c0001t0001g0112others(35): Show | 38 | HG00423.hp2 HG00597.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.*3+1027_*3+1028dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | ||||||
| chr4:37630356
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0002g0073a0001c0001t0005g0074 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.*3+1019_*3+1028dup others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | ||||||
| chr4:37630356
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0005g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*3+1018_*3+1028dup others(11): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | ||||||
| chr4:37630356
|
G | GTTTTTTT others(7): Show |
1 | a0001c0001t0005g0021 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.*3+1015_*3+1028dup others(14): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | ||||||
| chr4:37630356
|
GT | G | 24 | a0001c0001t0001g0306a0001c0001t0003g0131a0001c0001t0003g0170others(21): Show | 24 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.*3+1028delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630356 | ||||||
| chr4:37630367
|
T | G | 4 | a0001c0003t0019g0092a0001c0003t0019g0250a0001c0003t0019g0277others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.*3+1018A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630367 | ||||||
| chr4:37630368
|
T | G | 1 | a0001c0001t0003g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.*3+1017A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630368 | ||||||
| chr4:37630368
|
T | TG | 52 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.*3+1016_*3+1017ins others(1): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630368 | ||||||
| chr4:37630388
|
C | G | 1 | a0001c0001t0018g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.*3+997G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630388 | ||||||
| chr4:37630392
|
T | A | 1 | a0001c0001t0012g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.*3+993A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630392 | ||||||
| chr4:37630465
|
C | T | 1 | a0001c0001t0046g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.*3+920G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630465 | ||||||
| chr4:37630598
|
C | A | 53 | a0001c0001t0001g0298a0001c0001t0002g0042a0001c0001t0002g0045others(50): Show | 53 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.*3+787G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630598 | ||||||
| chr4:37630614
|
C | T | 3 | a0001c0001t0048g0256a0001c0006t0025g0023a0001c0006t0025g0252 | 3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*3+771G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630614 | ||||||
| chr4:37630616
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.*3+769G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630616 | ||||||
| chr4:37630688
|
T | C | 1 | a0001c0001t0002g0091 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.*3+697A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630688 | ||||||
| chr4:37630941
|
TA | T | 22 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(19): Show | 23 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.*3+443delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37630941 | ||||||
| chr4:37631373
|
A | G | 1 | a0001c0001t0004g0080 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.*3+12T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 6/6 | chr4 | 37631373 | ||||||
| chr4:37631601
|
A | C | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.681-78T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37631601 | ||||||
| chr4:37631647
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.681-124C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37631647 | ||||||
| chr4:37631886
|
A | C | 230 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(227): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.681-363T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37631886 | ||||||
| chr4:37631891
|
G | A | 19 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.681-368C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37631891 | ||||||
| chr4:37632051
|
C | G | 1 | a0001c0001t0067g0055 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.681-528G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632051 | ||||||
| chr4:37632079
|
A | G | 44 | a0001c0001t0003g0051a0001c0001t0003g0072a0001c0001t0003g0094others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.681-556T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632079 | ||||||
| chr4:37632084
|
G | GA | 63 | a0001c0001t0001g0046a0001c0001t0001g0082a0001c0001t0001g0140others(60): Show | 64 | HG00140.hp1 HG00741.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.681-562dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632084 | ||||||
| chr4:37632084
|
G | GAA | 106 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0002g0009others(103): Show | 107 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.681-563_681-562dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632084 | ||||||
| chr4:37632084
|
G | GAAA | 61 | a0001c0001t0002g0105a0001c0001t0002g0118a0001c0001t0002g0136others(58): Show | 62 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.681-564_681-562dup others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632084 | ||||||
| chr4:37632084
|
GA | G | 22 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0112others(19): Show | 22 | HG00642.hp1 HG01256.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.681-562delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632084 | ||||||
| chr4:37632114
|
T | G | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.681-591A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632114 | ||||||
| chr4:37632125
|
A | C | 1 | a0001c0001t0046g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681-602T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632125 | ||||||
| chr4:37632137
|
C | T | 41 | a0001c0001t0003g0051a0001c0001t0003g0072a0001c0001t0003g0094others(38): Show | 41 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.681-614G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632137 | ||||||
| chr4:37632150
|
G | A | 1 | a0001c0001t0046g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681-627C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632150 | ||||||
| chr4:37632171
|
T | TTTTG | 230 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(227): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.681-652_681-649dup others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632171 | ||||||
| chr4:37632241
|
G | A | 3 | a0001c0001t0048g0256a0001c0006t0025g0023a0001c0006t0025g0252 | 3 | HG02258.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.681-718C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632241 | ||||||
| chr4:37632342
|
T | C | 1 | a0001c0001t0046g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681-819A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632342 | ||||||
| chr4:37632345
|
AT | A | 81 | a0001c0001t0001g0298a0001c0001t0002g0009a0001c0001t0002g0042others(78): Show | 81 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.681-823delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632345 | ||||||
| chr4:37632403
|
C | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.681-880G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632403 | ||||||
| chr4:37632445
|
T | C | 87 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(84): Show | 88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.681-922A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632445 | ||||||
| chr4:37632534
|
C | T | 23 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(20): Show | 24 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.681-1011G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632534 | ||||||
| chr4:37632570
|
C | T | 62 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(59): Show | 63 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.681-1047G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632570 | ||||||
| chr4:37632572
|
A | G | 1 | a0001c0001t0003g0262 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.681-1049T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632572 | ||||||
| chr4:37632626
|
T | C | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.681-1103A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632626 | ||||||
| chr4:37632701
|
T | TA | 25 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(22): Show | 25 | HG00642.hp1 HG01175.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.681-1179dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632701 | ||||||
| chr4:37632915
|
T | G | 1 | a0001c0001t0004g0246 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.681-1392A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632915 | ||||||
| chr4:37632921
|
C | G | 41 | a0001c0001t0003g0051a0001c0001t0003g0072a0001c0001t0003g0094others(38): Show | 41 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.681-1398G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37632921 | ||||||
| chr4:37633087
|
A | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(52): Show | 56 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.681-1564T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633087 | ||||||
| chr4:37633136
|
C | T | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.681-1613G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633136 | ||||||
| chr4:37633179
|
C | G | 3 | a0001c0001t0016g0171a0001c0001t0022g0120a0001c0001t0022g0197 | 3 | HG02074.hp2 NA18942.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.681-1656G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633179 | ||||||
| chr4:37633183
|
T | C | 316 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(313): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.681-1660A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633183 | ||||||
| chr4:37633382
|
T | C | 54 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(51): Show | 55 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.680+1505A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633382 | ||||||
| chr4:37633408
|
CAAA | C | 9 | a0001c0001t0001g0126a0001c0001t0001g0150a0001c0001t0001g0185others(6): Show | 9 | HG01884.hp2 HG03579.hp1 NA18522.hp2 others(6): Show |
intron_variant | MODIFIER | c.680+1476_680+1478d others(5): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAA | C | 19 | a0001c0001t0001g0082a0001c0001t0001g0109a0001c0001t0001g0111others(16): Show | 19 | HG01081.hp2 HG01516.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.680+1475_680+1478d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAAA | C | 35 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(32): Show | 36 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.680+1474_680+1478d others(7): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAAAA | C | 18 | a0001c0001t0001g0112a0001c0001t0001g0249a0001c0001t0007g0241others(15): Show | 18 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.680+1473_680+1478d others(8): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAAAAA | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0033a0001c0001t0001g0273others(10): Show | 13 | HG01175.hp1 HG01515.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.680+1472_680+1478d others(9): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAAAAA others(1): Show |
C | 14 | a0001c0001t0001g0024a0001c0001t0001g0117a0001c0001t0001g0172others(11): Show | 14 | HG00642.hp1 HG01256.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.680+1471_680+1478d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAAAAA others(2): Show |
C | 30 | a0001c0001t0003g0094a0001c0001t0003g0106a0001c0001t0003g0108others(27): Show | 31 | HG01123.hp1 HG01192.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.680+1470_680+1478d others(11): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAAAAA others(3): Show |
C | 68 | a0001c0001t0001g0306a0001c0001t0003g0051a0001c0001t0003g0072others(65): Show | 70 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.680+1469_680+1478d others(12): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAAAAA others(4): Show |
C | 28 | a0001c0001t0004g0047a0001c0001t0004g0053a0001c0001t0004g0054others(25): Show | 28 | HG00140.hp1 HG00323.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.680+1468_680+1478d others(13): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAAAAA others(16): Show |
C | 3 | a0001c0001t0009g0174a0002c0005t0002g0186a0003c0004t0045g0006 | 3 | HG02970.hp2 NA19003.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.680+1456_680+1478d others(25): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633408
|
CAAAAAAA others(17): Show |
C | 79 | a0001c0001t0001g0298a0001c0001t0002g0009a0001c0001t0002g0042others(76): Show | 79 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.680+1455_680+1478d others(26): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633408 | ||||||
| chr4:37633451
|
T | C | 125 | a0001c0001t0001g0306a0001c0001t0003g0051a0001c0001t0003g0072others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.680+1436A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633451 | ||||||
| chr4:37633506
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.680+1381C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633506 | ||||||
| chr4:37633975
|
G | A | 2 | a0001c0001t0036g0293a0001c0001t0037g0254 | 2 | HG03209.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.680+912C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37633975 | ||||||
| chr4:37634014
|
C | T | 4 | a0001c0001t0008g0304a0001c0001t0014g0003a0001c0001t0014g0153others(1): Show | 5 | HG02056.hp1 HG02735.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.680+873G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634014 | ||||||
| chr4:37634068
|
G | T | 1 | a0001c0001t0005g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.680+819C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634068 | ||||||
| chr4:37634135
|
G | A | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.680+752C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634135 | ||||||
| chr4:37634188
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(181): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.680+699T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634188 | ||||||
| chr4:37634519
|
G | A | 1 | a0001c0001t0004g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.680+368C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634519 | ||||||
| chr4:37634592
|
A | G | 2 | a0001c0001t0005g0068a0001c0001t0005g0225 | 2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.680+295T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634592 | ||||||
| chr4:37634627
|
T | C | 4 | a0001c0001t0008g0304a0001c0001t0028g0012a0001c0001t0028g0271others(1): Show | 4 | HG02622.hp2 HG03704.hp1 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.680+260A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634627 | ||||||
| chr4:37634719
|
C | T | 48 | a0001c0001t0004g0030a0001c0001t0004g0047a0001c0001t0004g0053others(45): Show | 49 | HG00140.hp1 HG00741.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.680+168G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634719 | ||||||
| chr4:37634739
|
G | A | 19 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.680+148C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 5/6 | chr4 | 37634739 | ||||||
| chr4:37635128
|
T | G | 173 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(170): Show | 176 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(173): Show |
splice_region_variant&intron_variant | LOW | c.444-5A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635128 | ||||||
| chr4:37635222
|
GA | G | 8 | a0001c0001t0005g0287a0001c0001t0012g0135a0001c0001t0012g0141others(5): Show | 8 | HG02258.hp2 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.444-100delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635222 | ||||||
| chr4:37635300
|
C | A | 25 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(22): Show | 26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.444-177G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635300 | ||||||
| chr4:37635525
|
G | A | 9 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.444-402C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635525 | ||||||
| chr4:37635534
|
G | A | 5 | a0001c0001t0004g0085a0001c0001t0004g0086a0001c0001t0004g0165others(2): Show | 5 | HG01081.hp1 HG01346.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-411C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635534 | ||||||
| chr4:37635652
|
C | G | 1 | a0001c0001t0002g0127 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.444-529G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635652 | ||||||
| chr4:37635764
|
T | C | 2 | a0001c0001t0001g0298a0001c0001t0023g0297 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.444-641A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635764 | ||||||
| chr4:37635853
|
C | G | 2 | a0001c0001t0003g0115a0001c0001t0003g0130 | 2 | NA18966.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.444-730G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635853 | ||||||
| chr4:37635954
|
G | A | 29 | a0001c0001t0001g0306a0001c0001t0004g0242a0001c0001t0006g0104others(26): Show | 30 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.444-831C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635954 | ||||||
| chr4:37635968
|
T | C | 63 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(60): Show | 64 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.444-845A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37635968 | ||||||
| chr4:37636146
|
C | T | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.444-1023G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636146 | ||||||
| chr4:37636163
|
A | G | 1 | a0001c0001t0042g0211 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.444-1040T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636163 | ||||||
| chr4:37636205
|
C | T | 1 | a0001c0001t0003g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.444-1082G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636205 | ||||||
| chr4:37636260
|
G | C | 33 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(30): Show | 33 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.444-1137C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636260 | ||||||
| chr4:37636287
|
C | T | 1 | a0001c0001t0008g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.444-1164G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636287 | ||||||
| chr4:37636361
|
C | T | 5 | a0001c0001t0001g0046a0001c0001t0001g0128a0001c0001t0001g0193others(2): Show | 5 | HG00741.hp1 HG01081.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.444-1238G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636361 | ||||||
| chr4:37636413
|
A | G | 102 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(99): Show | 105 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.444-1290T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636413 | ||||||
| chr4:37636479
|
C | G | 1 | a0001c0001t0005g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.444-1356G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636479 | ||||||
| chr4:37636522
|
A | G | 171 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(168): Show | 174 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.444-1399T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636522 | ||||||
| chr4:37636526
|
C | T | 56 | a0001c0001t0001g0192a0001c0001t0002g0009a0001c0001t0002g0045others(53): Show | 56 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.444-1403G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636526 | ||||||
| chr4:37636554
|
C | T | 19 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.444-1431G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636554 | ||||||
| chr4:37636594
|
C | CA | 9 | a0001c0001t0005g0014a0001c0001t0024g0167a0001c0001t0031g0087others(6): Show | 9 | HG02027.hp1 HG03209.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.444-1472dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636594 | ||||||
| chr4:37636594
|
CA | C | 68 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(65): Show | 69 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.444-1472delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636594 | ||||||
| chr4:37636677
|
G | A | 2 | a0001c0001t0018g0002a0001c0001t0018g0025 | 3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.444-1554C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636677 | ||||||
| chr4:37636683
|
G | A | 1 | a0001c0001t0006g0176 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.444-1560C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636683 | ||||||
| chr4:37636790
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.443+1657G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37636790 | ||||||
| chr4:37637298
|
G | A | 26 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(23): Show | 27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.443+1149C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637298 | ||||||
| chr4:37637307
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0278 | 2 | NA18970.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.443+1140A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637307 | ||||||
| chr4:37637355
|
C | A | 3 | a0001c0001t0004g0056a0001c0001t0004g0057a0001c0001t0004g0075 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.443+1092G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637355 | ||||||
| chr4:37637450
|
A | C | 26 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(23): Show | 27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.443+997T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637450 | ||||||
| chr4:37637485
|
G | T | 3 | a0001c0001t0014g0003a0001c0001t0014g0153a0001c0001t0014g0294 | 4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+962C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637485 | ||||||
| chr4:37637517
|
C | T | 62 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(59): Show | 63 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.443+930G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637517 | ||||||
| chr4:37637705
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.443+742G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637705 | ||||||
| chr4:37637930
|
T | C | 3 | a0001c0001t0004g0242a0001c0001t0042g0211a0001c0001t0063g0289 | 3 | HG00323.hp2 HG01069.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.443+517A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637930 | ||||||
| chr4:37637944
|
C | G | 3 | a0001c0001t0001g0031a0001c0001t0008g0069a0001c0001t0061g0050 | 3 | HG01099.hp2 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.443+503G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37637944 | ||||||
| chr4:37638338
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.443+109C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37638338 | ||||||
| chr4:37638381
|
A | G | 2 | a0001c0001t0018g0002a0001c0001t0018g0025 | 3 | HG01167.hp2 HG01169.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.443+66T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37638381 | ||||||
| chr4:37638418
|
G | A | 1 | a0001c0001t0023g0095 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.443+29C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 4/6 | chr4 | 37638418 | ||||||
| chr4:37638643
|
G | A | 4 | a0001c0001t0013g0052a0001c0001t0013g0076a0001c0001t0068g0077others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-139C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638643 | ||||||
| chr4:37638670
|
G | A | 19 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.386-166C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638670 | ||||||
| chr4:37638706
|
T | C | 3 | a0001c0001t0004g0242a0001c0001t0042g0211a0001c0001t0063g0289 | 3 | HG00323.hp2 HG01069.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.386-202A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638706 | ||||||
| chr4:37638740
|
A | G | 4 | a0001c0003t0019g0092a0001c0003t0019g0250a0001c0003t0019g0277others(1): Show | 4 | HG01884.hp2 HG02723.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-236T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638740 | ||||||
| chr4:37638762
|
G | A | 43 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(40): Show | 43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.386-258C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638762 | ||||||
| chr4:37638767
|
T | C | 101 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(98): Show | 104 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-263A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638767 | ||||||
| chr4:37638861
|
C | A | 176 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(173): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.386-357G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638861 | ||||||
| chr4:37638905
|
T | C | 1 | a0001c0001t0004g0246 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.386-401A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638905 | ||||||
| chr4:37638921
|
A | G | 1 | a0001c0001t0006g0301 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.386-417T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37638921 | ||||||
| chr4:37639012
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0249a0001c0001t0001g0281others(1): Show | 4 | HG02486.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-508C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639012 | ||||||
| chr4:37639208
|
C | A | 26 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(23): Show | 27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.386-704G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639208 | ||||||
| chr4:37639315
|
C | T | 17 | a0001c0001t0004g0242a0001c0001t0012g0135a0001c0001t0012g0141others(14): Show | 19 | HG00323.hp2 HG01069.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.386-811G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639315 | ||||||
| chr4:37639340
|
C | T | 133 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.386-836G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639340 | ||||||
| chr4:37639354
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.386-850T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639354 | ||||||
| chr4:37639362
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.386-858G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639362 | ||||||
| chr4:37639363
|
G | A | 57 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(54): Show | 57 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.386-859C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639363 | ||||||
| chr4:37639383
|
C | CA | 62 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0112others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.386-880dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | ||||||
| chr4:37639383
|
C | CAA | 46 | a0001c0001t0001g0172a0001c0001t0001g0204a0001c0001t0001g0215others(43): Show | 48 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.386-881_386-880dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | ||||||
| chr4:37639383
|
C | CAAA | 6 | a0001c0001t0001g0117a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 6 | HG00323.hp2 HG01361.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-882_386-880dup others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | ||||||
| chr4:37639383
|
C | CAAAA | 7 | a0001c0001t0001g0015a0001c0001t0006g0104a0001c0001t0007g0132others(4): Show | 7 | HG01123.hp1 HG01175.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-883_386-880dup others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | ||||||
| chr4:37639383
|
CA | C | 46 | a0001c0001t0001g0043a0001c0001t0001g0185a0001c0001t0002g0091others(43): Show | 47 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.386-880delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | ||||||
| chr4:37639383
|
CAA | C | 8 | a0001c0001t0001g0109a0001c0001t0003g0106a0001c0001t0003g0115others(5): Show | 8 | HG00408.hp1 HG02258.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.386-881_386-880del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639383 | ||||||
| chr4:37639415
|
G | T | 5 | a0001c0001t0018g0002a0001c0001t0018g0025a0001c0001t0048g0256others(2): Show | 6 | HG01167.hp2 HG01169.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-911C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639415 | ||||||
| chr4:37639448
|
C | T | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.386-944G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639448 | ||||||
| chr4:37639521
|
C | CA | 43 | a0001c0001t0001g0158a0001c0001t0004g0047a0001c0001t0004g0053others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.386-1018dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639521 | ||||||
| chr4:37639521
|
C | CAA | 33 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(30): Show | 33 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.386-1019_386-1018d others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639521 | ||||||
| chr4:37639585
|
C | T | 1 | a0001c0001t0004g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.386-1081G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639585 | ||||||
| chr4:37639766
|
G | C | 1 | a0001c0001t0001g0267 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.386-1262C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639766 | ||||||
| chr4:37639816
|
A | C | 176 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(173): Show | 179 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.386-1312T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37639816 | ||||||
| chr4:37640017
|
A | G | 1 | a0001c0001t0014g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.386-1513T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640017 | ||||||
| chr4:37640071
|
G | GT | 14 | a0001c0001t0004g0030a0001c0001t0004g0083a0001c0001t0004g0123others(11): Show | 14 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.386-1568dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640071 | ||||||
| chr4:37640072
|
T | G | 4 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1568A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640072 | ||||||
| chr4:37640136
|
G | C | 4 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-1632C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640136 | ||||||
| chr4:37640468
|
C | T | 3 | a0001c0001t0014g0003a0001c0001t0014g0153a0001c0001t0014g0294 | 4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1964G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640468 | ||||||
| chr4:37640491
|
T | C | 5 | a0001c0001t0046g0319a0001c0003t0019g0092a0001c0003t0019g0250others(2): Show | 5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-1987A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640491 | ||||||
| chr4:37640715
|
G | A | 1 | a0001c0001t0003g0279 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.386-2211C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640715 | ||||||
| chr4:37640733
|
G | A | 317 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(314): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.386-2229C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640733 | ||||||
| chr4:37640747
|
AT | A | 105 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(102): Show | 108 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.386-2244delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640747 | ||||||
| chr4:37640802
|
T | A | 3 | a0001c0001t0004g0165a0001c0001t0004g0207a0001c0001t0057g0121 | 3 | HG01346.hp1 HG01358.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.386-2298A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640802 | ||||||
| chr4:37640812
|
A | G | 1 | a0001c0006t0025g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.386-2308T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640812 | ||||||
| chr4:37640845
|
C | T | 1 | a0001c0001t0036g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386-2341G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37640845 | ||||||
| chr4:37641124
|
G | A | 3 | a0001c0001t0004g0242a0001c0001t0042g0211a0001c0001t0063g0289 | 3 | HG00323.hp2 HG01069.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.386-2620C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641124 | ||||||
| chr4:37641245
|
A | C | 58 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(55): Show | 58 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.386-2741T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641245 | ||||||
| chr4:37641457
|
G | T | 4 | a0001c0001t0013g0052a0001c0001t0013g0076a0001c0001t0068g0077others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-2953C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641457 | ||||||
| chr4:37641570
|
A | G | 142 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(139): Show | 145 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.386-3066T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641570 | ||||||
| chr4:37641675
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.386-3171G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641675 | ||||||
| chr4:37641678
|
T | C | 2 | a0001c0001t0004g0242a0001c0001t0042g0211 | 2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.386-3174A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641678 | ||||||
| chr4:37641691
|
G | A | 1 | a0001c0001t0036g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.386-3187C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641691 | ||||||
| chr4:37641854
|
T | A | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.386-3350A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641854 | ||||||
| chr4:37641972
|
G | A | 15 | a0001c0001t0004g0030a0001c0001t0004g0083a0001c0001t0004g0123others(12): Show | 15 | HG00733.hp2 HG00741.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.386-3468C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641972 | ||||||
| chr4:37641979
|
C | T | 51 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(48): Show | 52 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.386-3475G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37641979 | ||||||
| chr4:37642073
|
A | G | 59 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(56): Show | 59 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.386-3569T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642073 | ||||||
| chr4:37642097
|
G | A | 11 | a0001c0001t0004g0242a0001c0001t0012g0135a0001c0001t0012g0141others(8): Show | 12 | HG00323.hp2 HG01069.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.386-3593C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642097 | ||||||
| chr4:37642163
|
G | C | 26 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(23): Show | 27 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.386-3659C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642163 | ||||||
| chr4:37642475
|
C | T | 3 | a0001c0001t0014g0003a0001c0001t0014g0153a0001c0001t0014g0294 | 4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-3971G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642475 | ||||||
| chr4:37642530
|
T | C | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.386-4026A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642530 | ||||||
| chr4:37642643
|
C | T | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.386-4139G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642643 | ||||||
| chr4:37642685
|
A | G | 318 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(315): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.386-4181T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642685 | ||||||
| chr4:37642929
|
A | C | 3 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0065g0145 | 3 | HG01081.hp2 HG01952.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.386-4425T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37642929 | ||||||
| chr4:37643019
|
T | C | 9 | a0001c0001t0004g0083a0001c0001t0004g0123a0001c0001t0004g0129others(6): Show | 9 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.385+4349A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643019 | ||||||
| chr4:37643264
|
CCAAA | C | 22 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(19): Show | 23 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.385+4100_385+4103d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643264 | ||||||
| chr4:37643393
|
C | T | 2 | a0001c0001t0004g0242a0001c0001t0042g0211 | 2 | HG00323.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.385+3975G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643393 | ||||||
| chr4:37643630
|
T | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0249a0001c0001t0001g0281others(1): Show | 4 | HG02486.hp2 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+3738A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643630 | ||||||
| chr4:37643638
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.385+3730A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643638 | ||||||
| chr4:37643767
|
C | T | 120 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(117): Show | 121 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.385+3601G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643767 | ||||||
| chr4:37643960
|
T | C | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.385+3408A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37643960 | ||||||
| chr4:37644017
|
G | A | 38 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(35): Show | 38 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.385+3351C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644017 | ||||||
| chr4:37644078
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.385+3290C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644078 | ||||||
| chr4:37644094
|
G | A | 33 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(30): Show | 33 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.385+3274C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644094 | ||||||
| chr4:37644172
|
A | T | 7 | a0001c0001t0010g0062a0001c0001t0010g0063a0001c0001t0010g0149others(4): Show | 7 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+3196T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644172 | ||||||
| chr4:37644200
|
C | A | 67 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.385+3168G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644200 | ||||||
| chr4:37644420
|
T | C | 3 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291 | 3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+2948A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644420 | ||||||
| chr4:37644438
|
T | TTTTA | 109 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0043others(106): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.385+2926_385+2929d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | ||||||
| chr4:37644438
|
T | TTTTATTT others(1): Show |
27 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0267others(24): Show | 27 | HG00323.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.385+2922_385+2929d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | ||||||
| chr4:37644438
|
T | TTTTATTT others(5): Show |
33 | a0001c0001t0001g0268a0001c0001t0004g0056a0001c0001t0004g0057others(30): Show | 34 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.385+2918_385+2929d others(14): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | ||||||
| chr4:37644438
|
T | TTTTATTT others(9): Show |
4 | a0001c0001t0001g0306a0001c0001t0004g0207a0001c0001t0013g0052others(1): Show | 4 | HG00408.hp2 HG00733.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+2914_385+2929d others(18): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | ||||||
| chr4:37644438
|
T | TTTTTTTT others(5): Show |
2 | a0001c0001t0006g0214a0001c0001t0006g0222 | 2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.385+2929_385+2930i others(14): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | ||||||
| chr4:37644438
|
TTTTA | T | 29 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(26): Show | 29 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.385+2926_385+2929d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | ||||||
| chr4:37644438
|
TTTTATTT others(1): Show |
T | 3 | a0001c0001t0004g0144a0001c0001t0018g0002a0001c0001t0018g0025 | 4 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+2922_385+2929d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | ||||||
| chr4:37644438
|
TTTTATTT others(5): Show |
T | 16 | a0001c0001t0001g0140a0001c0001t0001g0233a0001c0001t0001g0236others(13): Show | 16 | HG02027.hp1 HG02027.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.385+2918_385+2929d others(14): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | ||||||
| chr4:37644438
|
TTTTATTT others(9): Show |
T | 1 | a0001c0001t0002g0175 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385+2914_385+2929d others(18): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644438 | ||||||
| chr4:37644487
|
A | G | 1 | a0001c0001t0048g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.385+2881T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644487 | ||||||
| chr4:37644545
|
G | C | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+2823C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644545 | ||||||
| chr4:37644649
|
G | A | 5 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291others(2): Show | 5 | HG00140.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.385+2719C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644649 | ||||||
| chr4:37644662
|
G | A | 25 | a0001c0001t0004g0083a0001c0001t0004g0123a0001c0001t0004g0129others(22): Show | 26 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.385+2706C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644662 | ||||||
| chr4:37644672
|
C | T | 35 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(32): Show | 36 | HG00642.hp1 HG01106.hp2 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.385+2696G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644672 | ||||||
| chr4:37644914
|
G | A | 60 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(57): Show | 60 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.385+2454C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37644914 | ||||||
| chr4:37645074
|
C | T | 5 | a0001c0001t0046g0319a0001c0003t0019g0092a0001c0003t0019g0250others(2): Show | 5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+2294G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645074 | ||||||
| chr4:37645105
|
G | A | 1 | a0001c0001t0036g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385+2263C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645105 | ||||||
| chr4:37645119
|
C | T | 1 | a0001c0001t0004g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.385+2249G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645119 | ||||||
| chr4:37645137
|
A | G | 19 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.385+2231T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645137 | ||||||
| chr4:37645151
|
G | A | 5 | a0001c0001t0020g0018a0001c0001t0020g0019a0001c0001t0020g0027others(2): Show | 5 | HG02451.hp2 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+2217C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645151 | ||||||
| chr4:37645298
|
GC | G | 5 | a0001c0001t0020g0018a0001c0001t0020g0019a0001c0001t0020g0027others(2): Show | 5 | HG02451.hp2 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+2069delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645298 | ||||||
| chr4:37645299
|
C | G | 313 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(310): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.385+2069G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645299 | ||||||
| chr4:37645471
|
G | A | 47 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(44): Show | 48 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.385+1897C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645471 | ||||||
| chr4:37645518
|
T | A | 3 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291 | 3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+1850A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645518 | ||||||
| chr4:37645548
|
T | C | 60 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(57): Show | 60 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.385+1820A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645548 | ||||||
| chr4:37645611
|
C | A | 25 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(22): Show | 26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.385+1757G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645611 | ||||||
| chr4:37645612
|
G | A | 97 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(94): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.385+1756C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645612 | ||||||
| chr4:37645732
|
C | A | 97 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(94): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.385+1636G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645732 | ||||||
| chr4:37645771
|
C | T | 3 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291 | 3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+1597G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645771 | ||||||
| chr4:37645842
|
C | T | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.385+1526G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37645842 | ||||||
| chr4:37646115
|
T | C | 47 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(44): Show | 48 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.385+1253A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646115 | ||||||
| chr4:37646222
|
T | C | 97 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(94): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.385+1146A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646222 | ||||||
| chr4:37646274
|
G | T | 43 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(40): Show | 43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.385+1094C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646274 | ||||||
| chr4:37646341
|
T | C | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.385+1027A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646341 | ||||||
| chr4:37646433
|
G | C | 47 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(44): Show | 48 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.385+935C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646433 | ||||||
| chr4:37646456
|
G | T | 38 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(35): Show | 38 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.385+912C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646456 | ||||||
| chr4:37646562
|
G | C | 2 | a0001c0001t0005g0068a0001c0001t0005g0225 | 2 | HG02280.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.385+806C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646562 | ||||||
| chr4:37646709
|
A | G | 3 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291 | 3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+659T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646709 | ||||||
| chr4:37646792
|
A | C | 97 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(94): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.385+576T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646792 | ||||||
| chr4:37646793
|
T | C | 1 | a0001c0001t0005g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.385+575A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646793 | ||||||
| chr4:37646887
|
C | T | 25 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(22): Show | 26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.385+481G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37646887 | ||||||
| chr4:37647086
|
A | G | 149 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(146): Show | 151 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.385+282T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647086 | ||||||
| chr4:37647191
|
A | G | 174 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(171): Show | 177 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.385+177T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647191 | ||||||
| chr4:37647223
|
G | A | 38 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(35): Show | 38 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.385+145C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647223 | ||||||
| chr4:37647305
|
G | A | 1 | a0001c0001t0003g0139 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.385+63C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647305 | ||||||
| chr4:37647336
|
T | G | 5 | a0001c0001t0046g0319a0001c0003t0019g0092a0001c0003t0019g0250others(2): Show | 5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+32A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 3/6 | chr4 | 37647336 | ||||||
| chr4:37647670
|
A | C | 36 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.314-231T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647670 | ||||||
| chr4:37647711
|
T | C | 149 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(146): Show | 151 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.314-272A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647711 | ||||||
| chr4:37647781
|
G | T | 25 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(22): Show | 26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.314-342C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647781 | ||||||
| chr4:37647833
|
T | G | 1 | a0001c0001t0003g0279 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.314-394A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647833 | ||||||
| chr4:37647835
|
C | T | 96 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(93): Show | 97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.314-396G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647835 | ||||||
| chr4:37647844
|
T | C | 35 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(32): Show | 35 | HG00140.hp1 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.314-405A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37647844 | ||||||
| chr4:37648057
|
C | T | 1 | a0001c0001t0049g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.314-618G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648057 | ||||||
| chr4:37648140
|
C | T | 25 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(22): Show | 26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.314-701G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648140 | ||||||
| chr4:37648397
|
G | A | 1 | a0001c0001t0016g0166 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.313+879C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648397 | ||||||
| chr4:37648449
|
A | G | 1 | a0001c0001t0003g0169 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.313+827T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648449 | ||||||
| chr4:37648516
|
C | G | 1 | a0001c0001t0002g0127 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.313+760G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648516 | ||||||
| chr4:37648700
|
T | A | 1 | a0001c0001t0004g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.313+576A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648700 | ||||||
| chr4:37648810
|
C | T | 1 | a0001c0001t0037g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.313+466G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648810 | ||||||
| chr4:37648819
|
T | C | 1 | a0001c0001t0005g0224 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.313+457A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 2/6 | chr4 | 37648819 | ||||||
| chr4:37649533
|
A | G | 97 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(94): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.89-33T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37649533 | ||||||
| chr4:37650024
|
T | A | 96 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(93): Show | 97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.89-524A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650024 | ||||||
| chr4:37650037
|
T | C | 96 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(93): Show | 97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.89-537A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650037 | ||||||
| chr4:37650095
|
G | A | 41 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(38): Show | 41 | HG01081.hp1 HG01099.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.89-595C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650095 | ||||||
| chr4:37650106
|
C | G | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-606G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650106 | ||||||
| chr4:37650156
|
T | G | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-656A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650156 | ||||||
| chr4:37650192
|
G | A | 25 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(22): Show | 26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.89-692C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650192 | ||||||
| chr4:37650229
|
G | A | 8 | a0001c0001t0002g0073a0001c0001t0005g0007a0001c0001t0005g0014others(5): Show | 8 | HG01255.hp1 HG02280.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-729C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650229 | ||||||
| chr4:37650258
|
T | A | 96 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(93): Show | 97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.89-758A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650258 | ||||||
| chr4:37650441
|
C | A | 22 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(19): Show | 23 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.89-941G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650441 | ||||||
| chr4:37650886
|
C | A | 25 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(22): Show | 26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.89-1386G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650886 | ||||||
| chr4:37650887
|
C | G | 25 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(22): Show | 26 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.89-1387G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650887 | ||||||
| chr4:37650945
|
G | C | 2 | a0001c0001t0003g0217a0001c0001t0015g0133 | 2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.89-1445C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650945 | ||||||
| chr4:37650972
|
T | C | 1 | a0001c0001t0022g0120 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.89-1472A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650972 | ||||||
| chr4:37650973
|
T | C | 173 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(170): Show | 176 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.89-1473A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37650973 | ||||||
| chr4:37651057
|
C | CA | 10 | a0001c0001t0001g0046a0001c0001t0001g0125a0001c0001t0001g0126others(7): Show | 10 | HG00741.hp1 HG03139.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-1558dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651057 | ||||||
| chr4:37651057
|
CA | C | 28 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(25): Show | 29 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.89-1558delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651057 | ||||||
| chr4:37651057
|
CAA | C | 12 | a0001c0001t0015g0133a0001c0001t0020g0018a0001c0001t0020g0019others(9): Show | 12 | HG02258.hp2 HG02451.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-1559_89-1558del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651057 | ||||||
| chr4:37651057
|
CAAA | C | 132 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(129): Show | 134 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.89-1560_89-1558del others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651057 | ||||||
| chr4:37651076
|
A | T | 105 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(102): Show | 107 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.89-1576T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651076 | ||||||
| chr4:37651122
|
C | G | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-1622G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651122 | ||||||
| chr4:37651193
|
T | C | 121 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(118): Show | 123 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.89-1693A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651193 | ||||||
| chr4:37651202
|
T | A | 1 | a0001c0001t0004g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.89-1702A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651202 | ||||||
| chr4:37651323
|
C | A | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-1823G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651323 | ||||||
| chr4:37651406
|
T | A | 49 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(46): Show | 49 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.89-1906A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651406 | ||||||
| chr4:37651439
|
A | G | 96 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(93): Show | 97 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.89-1939T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651439 | ||||||
| chr4:37651548
|
T | C | 1 | a0001c0001t0013g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.89-2048A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651548 | ||||||
| chr4:37651658
|
C | A | 1 | a0001c0001t0006g0307 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.89-2158G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651658 | ||||||
| chr4:37651685
|
G | A | 1 | a0001c0001t0017g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.89-2185C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651685 | ||||||
| chr4:37651787
|
T | A | 2 | a0001c0001t0004g0231a0001c0001t0004g0232 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.89-2287A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651787 | ||||||
| chr4:37651866
|
C | T | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-2366G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651866 | ||||||
| chr4:37651884
|
G | A | 138 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(135): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.89-2384C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651884 | ||||||
| chr4:37651927
|
T | G | 1 | a0001c0001t0005g0021 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.89-2427A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37651927 | ||||||
| chr4:37652000
|
G | A | 37 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(34): Show | 37 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.89-2500C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652000 | ||||||
| chr4:37652027
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.89-2527G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652027 | ||||||
| chr4:37652034
|
G | A | 141 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(138): Show | 143 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.89-2534C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652034 | ||||||
| chr4:37652040
|
A | C | 7 | a0001c0001t0010g0062a0001c0001t0010g0063a0001c0001t0010g0149others(4): Show | 7 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-2540T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652040 | ||||||
| chr4:37652089
|
T | C | 30 | a0001c0001t0001g0107a0001c0001t0003g0051a0001c0001t0003g0072others(27): Show | 30 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.89-2589A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652089 | ||||||
| chr4:37652234
|
A | G | 1 | a0001c0001t0027g0247 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.89-2734T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652234 | ||||||
| chr4:37652284
|
C | T | 18 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.89-2784G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652284 | ||||||
| chr4:37652318
|
A | G | 191 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(188): Show | 194 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.89-2818T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652318 | ||||||
| chr4:37652382
|
A | G | 1 | a0001c0001t0001g0043 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.89-2882T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652382 | ||||||
| chr4:37652391
|
G | A | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-2891C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652391 | ||||||
| chr4:37652573
|
T | A | 139 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(136): Show | 141 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.89-3073A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652573 | ||||||
| chr4:37652628
|
G | A | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.89-3128C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652628 | ||||||
| chr4:37652738
|
A | G | 10 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0010g0062others(7): Show | 10 | HG02027.hp2 HG02074.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-3238T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652738 | ||||||
| chr4:37652796
|
C | T | 2 | a0001c0001t0004g0056a0001c0001t0004g0057 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.89-3296G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652796 | ||||||
| chr4:37652858
|
G | T | 33 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(30): Show | 34 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.89-3358C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652858 | ||||||
| chr4:37652959
|
G | C | 3 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291 | 3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.89-3459C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37652959 | ||||||
| chr4:37653198
|
C | T | 1 | a0001c0001t0013g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.89-3698G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653198 | ||||||
| chr4:37653235
|
T | G | 1 | a0001c0001t0007g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.89-3735A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653235 | ||||||
| chr4:37653313
|
T | TGTATTGA others(13): Show |
5 | a0001c0001t0004g0242a0001c0001t0012g0135a0001c0001t0012g0141others(2): Show | 5 | HG00323.hp2 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-3833_89-3814dup others(20): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653313 | ||||||
| chr4:37653317
|
T | C | 1 | a0001c0001t0049g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.89-3817A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653317 | ||||||
| chr4:37653324
|
CTCAATAC others(40): Show |
C | 4 | a0001c0001t0001g0313a0001c0001t0007g0137a0001c0001t0028g0012others(1): Show | 4 | HG02622.hp2 HG03017.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-3871_89-3825del others(47): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653324 | ||||||
| chr4:37653344
|
CTCAATAC others(20): Show |
C | 195 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(192): Show | 196 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.89-3871_89-3845del others(27): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653344 | ||||||
| chr4:37653344
|
CTCAATAC others(47): Show |
C | 1 | a0001c0001t0003g0108 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.89-3898_89-3845del others(54): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653344 | ||||||
| chr4:37653364
|
CTCAATAT | C | 64 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(61): Show | 64 | HG00099.hp1 HG00408.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.89-3871_89-3865del others(7): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653364 | ||||||
| chr4:37653370
|
A | ACAAGTAT others(6): Show |
39 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(36): Show | 42 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.89-3871_89-3870ins others(13): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653370 | ||||||
| chr4:37653370
|
A | ACAAGTAT others(26): Show |
3 | a0001c0001t0004g0206a0001c0001t0004g0229a0004c0008t0004g0265 | 3 | HG00140.hp1 HG01192.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.89-3871_89-3870ins others(33): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653370 | ||||||
| chr4:37653371
|
T | C | 42 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(39): Show | 45 | HG00140.hp1 HG00741.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.89-3871A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653371 | ||||||
| chr4:37653375
|
A | G | 1 | a0001c0001t0023g0095 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.89-3875T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653375 | ||||||
| chr4:37653415
|
A | AT | 3 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291 | 3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.89-3916_89-3915ins others(1): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653415 | ||||||
| chr4:37653416
|
A | T | 6 | a0001c0001t0046g0319a0001c0001t0063g0289a0001c0003t0019g0092others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3916T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653416 | ||||||
| chr4:37653417
|
C | A | 6 | a0001c0001t0046g0319a0001c0001t0063g0289a0001c0003t0019g0092others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-3917G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653417 | ||||||
| chr4:37653417
|
C | CCTCAATA others(47): Show |
1 | a0001c0001t0048g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89-3918_89-3917ins others(54): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653417 | ||||||
| chr4:37653417
|
C | CTCAATAT others(19): Show |
3 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291 | 3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.89-3918_89-3917ins others(26): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653417 | ||||||
| chr4:37653493
|
A | C | 3 | a0001c0001t0004g0086a0001c0001t0021g0059a0001c0001t0021g0079 | 3 | HG01081.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.89-3993T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653493 | ||||||
| chr4:37653675
|
C | G | 1 | a0001c0001t0004g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-4175G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653675 | ||||||
| chr4:37653768
|
A | T | 133 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(130): Show | 135 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.89-4268T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653768 | ||||||
| chr4:37653872
|
C | T | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.89-4372G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653872 | ||||||
| chr4:37653921
|
A | G | 1 | a0001c0001t0049g0255 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.89-4421T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37653921 | ||||||
| chr4:37654031
|
T | A | 1 | a0001c0001t0006g0190 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.89-4531A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654031 | ||||||
| chr4:37654186
|
T | C | 1 | a0001c0001t0004g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-4686A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654186 | ||||||
| chr4:37654573
|
C | T | 1 | a0001c0003t0019g0250 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.89-5073G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654573 | ||||||
| chr4:37654615
|
G | T | 18 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(15): Show | 18 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.89-5115C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654615 | ||||||
| chr4:37654648
|
T | C | 1 | a0001c0001t0003g0106 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.89-5148A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654648 | ||||||
| chr4:37654668
|
A | T | 27 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(24): Show | 28 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.89-5168T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654668 | ||||||
| chr4:37654704
|
G | A | 170 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(167): Show | 173 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.89-5204C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654704 | ||||||
| chr4:37654837
|
T | G | 63 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(60): Show | 63 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.89-5337A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654837 | ||||||
| chr4:37654881
|
G | A | 1 | a0001c0001t0048g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89-5381C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37654881 | ||||||
| chr4:37655242
|
A | AAT | 3 | a0001c0001t0002g0296a0001c0001t0004g0165a0001c0001t0057g0121 | 3 | HG01358.hp1 HG03710.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.89-5744_89-5743dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655242 | ||||||
| chr4:37655242
|
A | AATAT | 4 | a0001c0001t0001g0192a0001c0001t0002g0316a0001c0001t0003g0122others(1): Show | 4 | HG00558.hp2 HG00621.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-5746_89-5743dup others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655242 | ||||||
| chr4:37655242
|
AAT | A | 140 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(137): Show | 142 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.89-5744_89-5743del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655242 | ||||||
| chr4:37655262
|
A | T | 1 | a0001c0001t0038g0154 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.89-5762T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655262 | ||||||
| chr4:37655497
|
C | T | 1 | a0001c0001t0020g0027 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.89-5997G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655497 | ||||||
| chr4:37655507
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.89-6007G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655507 | ||||||
| chr4:37655517
|
C | A | 2 | a0001c0001t0055g0026a0001c0001t0056g0010 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.89-6017G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655517 | ||||||
| chr4:37655602
|
C | T | 3 | a0001c0001t0032g0097a0001c0001t0032g0119a0001c0001t0070g0164 | 3 | NA18942.hp1 NA18995.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.89-6102G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655602 | ||||||
| chr4:37655675
|
C | T | 1 | a0001c0001t0048g0256 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89-6175G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655675 | ||||||
| chr4:37655821
|
G | C | 5 | a0001c0001t0046g0319a0001c0003t0019g0092a0001c0003t0019g0250others(2): Show | 5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-6321C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655821 | ||||||
| chr4:37655921
|
G | A | 2 | a0001c0006t0025g0023a0001c0006t0025g0252 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.89-6421C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655921 | ||||||
| chr4:37655952
|
G | A | 35 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(32): Show | 36 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.89-6452C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655952 | ||||||
| chr4:37655975
|
A | G | 2 | a0001c0001t0003g0180a0001c0001t0015g0143 | 2 | NA18994.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.89-6475T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37655975 | ||||||
| chr4:37656116
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0001g0282 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.89-6616C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656116 | ||||||
| chr4:37656159
|
T | A | 2 | a0001c0001t0001g0298a0001c0001t0023g0297 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.89-6659A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656159 | ||||||
| chr4:37656164
|
T | C | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-6664A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656164 | ||||||
| chr4:37656251
|
C | T | 6 | a0001c0001t0001g0226a0001c0001t0002g0073a0001c0001t0005g0007others(3): Show | 6 | HG01255.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-6751G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656251 | ||||||
| chr4:37656324
|
T | G | 2 | a0001c0006t0025g0023a0001c0006t0025g0252 | 2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.89-6824A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656324 | ||||||
| chr4:37656348
|
G | A | 3 | a0001c0001t0003g0155a0001c0001t0003g0217a0001c0001t0015g0133 | 3 | HG02132.hp2 NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.89-6848C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656348 | ||||||
| chr4:37656366
|
G | A | 3 | a0001c0001t0006g0157a0001c0001t0006g0301a0001c0001t0006g0307 | 3 | HG02129.hp1 HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.89-6866C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656366 | ||||||
| chr4:37656568
|
C | A | 1 | a0001c0001t0004g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-7068G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656568 | ||||||
| chr4:37656583
|
G | A | 1 | a0001c0001t0008g0008 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.89-7083C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656583 | ||||||
| chr4:37656601
|
A | G | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-7101T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656601 | ||||||
| chr4:37656611
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.89-7111C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656611 | ||||||
| chr4:37656653
|
G | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-7153C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656653 | ||||||
| chr4:37656752
|
C | T | 1 | a0001c0001t0073g0044 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.89-7252G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656752 | ||||||
| chr4:37656753
|
G | C | 1 | a0001c0001t0037g0254 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.89-7253C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656753 | ||||||
| chr4:37656804
|
T | C | 1 | a0001c0001t0026g0280 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.89-7304A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656804 | ||||||
| chr4:37656878
|
A | G | 11 | a0001c0001t0004g0206a0001c0001t0004g0229a0001c0001t0005g0017others(8): Show | 11 | HG00140.hp1 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-7378T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37656878 | ||||||
| chr4:37657100
|
T | C | 3 | a0001c0001t0008g0209a0001c0001t0008g0257a0001c0001t0029g0114 | 3 | HG02258.hp1 HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.89-7600A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657100 | ||||||
| chr4:37657135
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.89-7635T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657135 | ||||||
| chr4:37657144
|
A | C | 1 | a0001c0001t0004g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.89-7644T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657144 | ||||||
| chr4:37657317
|
C | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-7817G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657317 | ||||||
| chr4:37657480
|
G | T | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-7980C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657480 | ||||||
| chr4:37657526
|
C | T | 1 | a0001c0001t0004g0206 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.89-8026G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657526 | ||||||
| chr4:37657616
|
G | T | 39 | a0001c0001t0004g0053a0001c0001t0004g0054a0001c0001t0004g0056others(36): Show | 41 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.89-8116C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657616 | ||||||
| chr4:37657635
|
C | T | 35 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(32): Show | 36 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.89-8135G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657635 | ||||||
| chr4:37657754
|
A | G | 11 | a0001c0001t0004g0206a0001c0001t0004g0229a0001c0001t0005g0017others(8): Show | 11 | HG00140.hp1 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-8254T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657754 | ||||||
| chr4:37657885
|
G | A | 3 | a0001c0001t0006g0104a0001c0001t0006g0235a0001c0001t0026g0173 | 3 | HG01123.hp1 HG01346.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.89-8385C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657885 | ||||||
| chr4:37657894
|
G | C | 5 | a0001c0001t0046g0319a0001c0003t0019g0092a0001c0003t0019g0250others(2): Show | 5 | HG01884.hp2 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.89-8394C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657894 | ||||||
| chr4:37657998
|
A | G | 1 | a0001c0001t0004g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.89-8498T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37657998 | ||||||
| chr4:37658113
|
G | A | 35 | a0001c0001t0001g0306a0001c0001t0006g0104a0001c0001t0006g0142others(32): Show | 36 | HG00408.hp2 HG00544.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.89-8613C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658113 | ||||||
| chr4:37658255
|
C | A | 1 | a0001c0001t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.89-8755G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658255 | ||||||
| chr4:37658356
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.89-8856G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658356 | ||||||
| chr4:37658386
|
C | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-8886G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658386 | ||||||
| chr4:37658464
|
C | T | 3 | a0001c0001t0014g0003a0001c0001t0014g0153a0001c0001t0014g0294 | 4 | HG02056.hp1 HG02735.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-8964G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658464 | ||||||
| chr4:37658601
|
C | A | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.89-9101G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658601 | ||||||
| chr4:37658660
|
C | T | 11 | a0001c0001t0004g0206a0001c0001t0004g0229a0001c0001t0005g0017others(8): Show | 11 | HG00140.hp1 HG01192.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.89-9160G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658660 | ||||||
| chr4:37658688
|
G | A | 3 | a0001c0001t0012g0135a0001c0001t0012g0141a0001c0001t0012g0291 | 3 | HG02572.hp2 HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.89-9188C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658688 | ||||||
| chr4:37658782
|
G | A | 32 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(29): Show | 32 | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.89-9282C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658782 | ||||||
| chr4:37658993
|
G | A | 94 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(91): Show | 96 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.89-9493C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37658993 | ||||||
| chr4:37659154
|
A | G | 22 | a0001c0001t0001g0306a0001c0001t0003g0221a0001c0001t0006g0142others(19): Show | 23 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.89-9654T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659154 | ||||||
| chr4:37659172
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.89-9672G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659172 | ||||||
| chr4:37659211
|
G | A | 53 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0033others(50): Show | 55 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.89-9711C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659211 | ||||||
| chr4:37659220
|
A | G | 318 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(315): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.89-9720T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659220 | ||||||
| chr4:37659278
|
A | G | 5 | a0001c0002t0005g0064a0001c0002t0011g0001a0001c0002t0011g0065others(2): Show | 6 | HG01168.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-9778T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659278 | ||||||
| chr4:37659310
|
T | A | 1 | a0001c0001t0004g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.89-9810A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659310 | ||||||
| chr4:37659452
|
G | A | 21 | a0001c0001t0001g0306a0001c0001t0006g0157a0001c0001t0006g0176others(18): Show | 22 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.89-9952C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659452 | ||||||
| chr4:37659461
|
T | C | 1 | a0001c0001t0036g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.89-9961A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659461 | ||||||
| chr4:37659479
|
T | C | 7 | a0001c0001t0001g0249a0001c0001t0005g0035a0001c0001t0020g0018others(4): Show | 7 | HG02486.hp2 HG02622.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.89-9979A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659479 | ||||||
| chr4:37659518
|
T | A | 1 | a0001c0001t0003g0108 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.89-10018A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659518 | ||||||
| chr4:37659609
|
C | G | 3 | a0001c0001t0005g0014a0001c0001t0005g0068a0001c0001t0009g0028 | 3 | HG02280.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.89-10109G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659609 | ||||||
| chr4:37659737
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89-10237A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659737 | ||||||
| chr4:37659848
|
G | A | 17 | a0001c0001t0001g0306a0001c0001t0002g0091a0001c0001t0002g0296others(14): Show | 17 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.89-10348C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37659848 | ||||||
| chr4:37660041
|
TG | T | 6 | a0001c0001t0001g0024a0001c0001t0005g0035a0001c0001t0020g0018others(3): Show | 6 | HG02723.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-10542delC | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660041 | ||||||
| chr4:37660104
|
GC | G | 22 | a0001c0001t0001g0199a0001c0001t0001g0270a0001c0001t0001g0311others(19): Show | 22 | HG00597.hp2 HG01074.hp2 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.89-10605delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660104 | ||||||
| chr4:37660145
|
T | C | 21 | a0001c0001t0001g0199a0001c0001t0001g0270a0001c0001t0001g0311others(18): Show | 21 | HG01074.hp2 HG01975.hp2 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.89-10645A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660145 | ||||||
| chr4:37660152
|
G | C | 1 | a0001c0001t0006g0176 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.89-10652C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660152 | ||||||
| chr4:37660162
|
A | T | 30 | a0001c0001t0001g0249a0001c0001t0001g0260a0001c0001t0001g0317others(27): Show | 31 | HG00099.hp1 HG01081.hp1 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.89-10662T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660162 | ||||||
| chr4:37660232
|
G | C | 1 | a0001c0001t0002g0136 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.89-10732C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660232 | ||||||
| chr4:37660265
|
G | A | 2 | a0001c0001t0004g0053a0001c0001t0004g0245 | 2 | HG03688.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.89-10765C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660265 | ||||||
| chr4:37660401
|
C | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0081others(7): Show | 10 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-10901G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660401 | ||||||
| chr4:37660669
|
C | T | 9 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0002g0183others(6): Show | 10 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-11169G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660669 | ||||||
| chr4:37660678
|
C | A | 11 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0081others(8): Show | 11 | HG00099.hp1 HG00642.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.89-11178G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660678 | ||||||
| chr4:37660754
|
G | A | 1 | a0001c0001t0002g0163 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.89-11254C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660754 | ||||||
| chr4:37660758
|
G | A | 295 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(292): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.89-11258C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660758 | ||||||
| chr4:37660766
|
T | A | 66 | a0001c0001t0001g0046a0001c0001t0001g0088a0001c0001t0001g0107others(63): Show | 67 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.89-11266A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660766 | ||||||
| chr4:37660769
|
C | T | 1 | a0001c0001t0003g0212 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.89-11269G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660769 | ||||||
| chr4:37660797
|
C | T | 1 | a0001c0001t0041g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.89-11297G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660797 | ||||||
| chr4:37660798
|
A | G | 2 | a0001c0001t0041g0216a0001c0001t0062g0048 | 2 | HG00438.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.89-11298T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660798 | ||||||
| chr4:37660807
|
A | G | 1 | a0001c0001t0041g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.89-11307T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660807 | ||||||
| chr4:37660821
|
G | A | 4 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0075g0314others(1): Show | 4 | HG02071.hp1 HG02129.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.89-11321C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660821 | ||||||
| chr4:37660839
|
G | A | 91 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0031others(88): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.89-11339C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660839 | ||||||
| chr4:37660848
|
G | A | 16 | a0001c0001t0001g0193a0001c0001t0001g0213a0001c0001t0002g0103others(13): Show | 16 | HG00733.hp1 HG01081.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.89-11348C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660848 | ||||||
| chr4:37660899
|
C | T | 171 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(168): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.89-11399G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660899 | ||||||
| chr4:37660904
|
G | T | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.89-11404C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660904 | ||||||
| chr4:37660910
|
T | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.89-11410A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660910 | ||||||
| chr4:37660956
|
G | A | 1 | a0001c0001t0003g0177 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.89-11456C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660956 | ||||||
| chr4:37660974
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.89-11474A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660974 | ||||||
| chr4:37660979
|
C | T | 42 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0172others(39): Show | 43 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.89-11479G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660979 | ||||||
| chr4:37660980
|
G | A | 3 | a0001c0001t0004g0054a0001c0001t0005g0068a0001c0001t0018g0002 | 4 | HG01167.hp2 HG01169.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-11480C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37660980 | ||||||
| chr4:37661009
|
T | C | 1 | a0001c0001t0003g0122 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.89-11509A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661009 | ||||||
| chr4:37661025
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.89-11525A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661025 | ||||||
| chr4:37661030
|
C | CA | 9 | a0001c0001t0001g0031a0001c0001t0005g0007a0001c0001t0005g0014others(6): Show | 10 | HG01099.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.89-11531dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661030 | ||||||
| chr4:37661148
|
C | A | 2 | a0001c0001t0002g0261a0001c0001t0052g0264 | 2 | NA18939.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.89-11648G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661148 | ||||||
| chr4:37661181
|
T | C | 2 | a0001c0001t0003g0230a0001c0001t0006g0234 | 2 | NA18941.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.89-11681A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661181 | ||||||
| chr4:37661267
|
C | CTGTT | 49 | a0001c0001t0001g0015a0001c0001t0001g0172a0001c0001t0001g0202others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.89-11771_89-11768d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661267 | ||||||
| chr4:37661267
|
C | CTGTTTGT others(1): Show |
28 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(25): Show | 28 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.89-11775_89-11768d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661267 | ||||||
| chr4:37661267
|
CTGTT | C | 44 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0033others(41): Show | 46 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.89-11771_89-11768d others(6): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661267 | ||||||
| chr4:37661324
|
C | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.89-11824G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661324 | ||||||
| chr4:37661424
|
C | T | 14 | a0001c0001t0001g0107a0001c0001t0001g0270a0001c0001t0002g0098others(11): Show | 14 | HG00621.hp2 HG01257.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.89-11924G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661424 | ||||||
| chr4:37661517
|
C | A | 1 | a0001c0001t0003g0259 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.89-12017G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661517 | ||||||
| chr4:37661560
|
G | A | 2 | a0001c0001t0001g0233a0001c0001t0009g0028 | 2 | NA18970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.89-12060C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37661560 | ||||||
| chr4:37662021
|
G | C | 118 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(115): Show | 119 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.89-12521C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662021 | ||||||
| chr4:37662050
|
T | A | 53 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.89-12550A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662050 | ||||||
| chr4:37662126
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.89-12626G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662126 | ||||||
| chr4:37662300
|
A | G | 12 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(9): Show | 12 | HG00140.hp1 HG02040.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.89-12800T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662300 | ||||||
| chr4:37662488
|
A | G | 38 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(35): Show | 39 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.89-12988T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662488 | ||||||
| chr4:37662520
|
G | A | 53 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.89-13020C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662520 | ||||||
| chr4:37662578
|
TA | T | 110 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.89-13079delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662578 | ||||||
| chr4:37662697
|
G | A | 33 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(30): Show | 33 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.89-13197C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662697 | ||||||
| chr4:37662734
|
A | C | 27 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(24): Show | 27 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-13234T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662734 | ||||||
| chr4:37662961
|
G | T | 10 | a0001c0001t0001g0172a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.89-13461C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37662961 | ||||||
| chr4:37663055
|
A | G | 116 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.89-13555T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663055 | ||||||
| chr4:37663095
|
C | T | 65 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(62): Show | 66 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.89-13595G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663095 | ||||||
| chr4:37663115
|
G | A | 3 | a0001c0001t0037g0254a0001c0001t0048g0256a0001c0001t0049g0255 | 3 | HG02451.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.89-13615C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663115 | ||||||
| chr4:37663175
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.89-13675G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663175 | ||||||
| chr4:37663176
|
T | C | 45 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.89-13676A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663176 | ||||||
| chr4:37663279
|
C | T | 1 | a0001c0001t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-13779G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663279 | ||||||
| chr4:37663422
|
A | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.89-13922T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663422 | ||||||
| chr4:37663422
|
A | T | 1 | a0003c0004t0045g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.89-13922T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663422 | ||||||
| chr4:37663658
|
C | T | 190 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0041others(187): Show | 193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.89-14158G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663658 | ||||||
| chr4:37663738
|
C | T | 4 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0066g0272others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-14238G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663738 | ||||||
| chr4:37663763
|
T | A | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.89-14263A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663763 | ||||||
| chr4:37663861
|
C | A | 65 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(62): Show | 66 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.89-14361G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663861 | ||||||
| chr4:37663950
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.89-14450A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37663950 | ||||||
| chr4:37664046
|
A | G | 1 | a0001c0001t0007g0241 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.89-14546T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664046 | ||||||
| chr4:37664095
|
C | T | 2 | a0001c0001t0005g0007a0001c0001t0005g0014 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.89-14595G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664095 | ||||||
| chr4:37664117
|
C | G | 62 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(59): Show | 63 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.89-14617G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664117 | ||||||
| chr4:37664194
|
G | T | 1 | a0001c0007t0030g0090 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.89-14694C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664194 | ||||||
| chr4:37664348
|
C | G | 65 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(62): Show | 66 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.89-14848G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664348 | ||||||
| chr4:37664369
|
T | C | 7 | a0001c0001t0005g0253a0001c0001t0008g0257a0001c0001t0037g0254others(4): Show | 7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-14869A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664369 | ||||||
| chr4:37664372
|
CA | C | 84 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(81): Show | 85 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.89-14873delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664372 | ||||||
| chr4:37664388
|
T | C | 5 | a0001c0001t0002g0136a0001c0001t0006g0190a0001c0001t0010g0138others(2): Show | 5 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-14888A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664388 | ||||||
| chr4:37664433
|
G | T | 1 | a0001c0001t0021g0029 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.89-14933C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664433 | ||||||
| chr4:37664489
|
T | C | 1 | a0001c0001t0002g0096 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.89-14989A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664489 | ||||||
| chr4:37664557
|
T | C | 1 | a0001c0001t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-15057A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664557 | ||||||
| chr4:37664806
|
G | A | 1 | a0001c0001t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-15306C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664806 | ||||||
| chr4:37664901
|
G | A | 7 | a0001c0001t0005g0253a0001c0001t0008g0257a0001c0001t0037g0254others(4): Show | 7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-15401C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37664901 | ||||||
| chr4:37665006
|
C | T | 1 | a0001c0001t0015g0071 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.89-15506G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665006 | ||||||
| chr4:37665173
|
T | G | 8 | a0001c0001t0001g0308a0001c0001t0001g0311a0001c0001t0002g0299others(5): Show | 8 | HG00423.hp2 HG01106.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-15673A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665173 | ||||||
| chr4:37665354
|
C | G | 58 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(55): Show | 59 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.89-15854G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665354 | ||||||
| chr4:37665369
|
T | G | 117 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(114): Show | 118 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.89-15869A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665369 | ||||||
| chr4:37665374
|
A | C | 27 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(24): Show | 27 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-15874T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665374 | ||||||
| chr4:37665470
|
A | T | 6 | a0001c0001t0001g0199a0001c0001t0002g0127a0001c0001t0002g0201others(3): Show | 6 | HG01074.hp2 NA18950.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-15970T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665470 | ||||||
| chr4:37665519
|
C | T | 2 | a0001c0001t0036g0293a0001c0001t0046g0319 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.89-16019G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665519 | ||||||
| chr4:37665607
|
C | G | 4 | a0001c0001t0001g0273a0001c0001t0001g0276a0001c0001t0066g0272others(1): Show | 4 | HG02257.hp1 HG02630.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-16107G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665607 | ||||||
| chr4:37665674
|
C | A | 23 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(20): Show | 23 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.89-16174G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665674 | ||||||
| chr4:37665722
|
C | T | 2 | a0001c0001t0003g0101a0001c0001t0003g0168 | 2 | HG00621.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.89-16222G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665722 | ||||||
| chr4:37665747
|
G | A | 1 | a0001c0001t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-16247C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665747 | ||||||
| chr4:37665806
|
G | A | 103 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(100): Show | 104 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.89-16306C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665806 | ||||||
| chr4:37665819
|
T | A | 2 | a0001c0001t0003g0217a0001c0001t0015g0133 | 2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.89-16319A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665819 | ||||||
| chr4:37665895
|
T | C | 43 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(40): Show | 43 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.89-16395A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665895 | ||||||
| chr4:37665901
|
A | G | 60 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(57): Show | 61 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.89-16401T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37665901 | ||||||
| chr4:37666205
|
G | C | 37 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(34): Show | 37 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.89-16705C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666205 | ||||||
| chr4:37666242
|
A | G | 40 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(37): Show | 40 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.89-16742T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666242 | ||||||
| chr4:37666287
|
C | T | 15 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0002g0105others(12): Show | 15 | HG00673.hp1 HG01123.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.89-16787G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666287 | ||||||
| chr4:37666288
|
G | A | 2 | a0001c0001t0036g0293a0001c0001t0046g0319 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.89-16788C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666288 | ||||||
| chr4:37666362
|
C | T | 1 | a0001c0001t0075g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.89-16862G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666362 | ||||||
| chr4:37666541
|
T | C | 23 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(20): Show | 23 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.89-17041A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666541 | ||||||
| chr4:37666853
|
G | A | 2 | a0001c0001t0013g0076a0001c0001t0068g0077 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.89-17353C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666853 | ||||||
| chr4:37666862
|
A | G | 71 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(68): Show | 71 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.89-17362T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666862 | ||||||
| chr4:37666915
|
G | A | 3 | a0001c0001t0006g0152a0001c0001t0014g0003a0001c0001t0014g0153 | 4 | HG02735.hp1 HG03491.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.89-17415C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37666915 | ||||||
| chr4:37667008
|
G | A | 8 | a0001c0001t0003g0051a0001c0001t0003g0072a0001c0001t0010g0062others(5): Show | 8 | HG01928.hp2 HG01975.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.89-17508C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667008 | ||||||
| chr4:37667033
|
A | T | 1 | a0001c0001t0003g0155 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.89-17533T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667033 | ||||||
| chr4:37667044
|
G | C | 3 | a0001c0001t0001g0317a0001c0001t0002g0261a0001c0001t0052g0264 | 3 | HG02040.hp1 NA18939.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.89-17544C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667044 | ||||||
| chr4:37667054
|
G | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.89-17554C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667054 | ||||||
| chr4:37667090
|
A | G | 1 | a0001c0001t0007g0310 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.89-17590T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667090 | ||||||
| chr4:37667125
|
C | T | 1 | a0001c0001t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.89-17625G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667125 | ||||||
| chr4:37667126
|
G | A | 20 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0004g0030others(17): Show | 20 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.89-17626C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667126 | ||||||
| chr4:37667163
|
A | C | 2 | a0001c0001t0015g0251a0001c0006t0025g0252 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.89-17663T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667163 | ||||||
| chr4:37667221
|
G | A | 1 | a0001c0001t0004g0058 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.89-17721C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667221 | ||||||
| chr4:37667275
|
T | G | 3 | a0001c0001t0008g0016a0001c0001t0008g0022a0001c0006t0025g0023 | 3 | HG01167.hp1 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.89-17775A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667275 | ||||||
| chr4:37667581
|
G | A | 1 | a0003c0004t0035g0005 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.89-18081C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667581 | ||||||
| chr4:37667735
|
CT | C | 34 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(31): Show | 34 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.89-18236delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667735 | ||||||
| chr4:37667875
|
C | G | 103 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(100): Show | 104 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.88+18325G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667875 | ||||||
| chr4:37667951
|
A | G | 71 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(68): Show | 71 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.88+18249T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37667951 | ||||||
| chr4:37668076
|
G | C | 2 | a0001c0001t0005g0253a0001c0001t0008g0257 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88+18124C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668076 | ||||||
| chr4:37668079
|
AT | A | 34 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(31): Show | 35 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.88+18120delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668079 | ||||||
| chr4:37668213
|
T | C | 1 | a0001c0001t0064g0240 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.88+17987A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668213 | ||||||
| chr4:37668227
|
T | C | 1 | a0001c0001t0008g0304 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.88+17973A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668227 | ||||||
| chr4:37668261
|
A | G | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.88+17939T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668261 | ||||||
| chr4:37668263
|
C | A | 1 | a0001c0001t0005g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+17937G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668263 | ||||||
| chr4:37668264
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0050g0013 | 2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.88+17936C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668264 | ||||||
| chr4:37668268
|
C | G | 4 | a0001c0001t0013g0052a0001c0001t0013g0076a0001c0001t0013g0078others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+17932G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668268 | ||||||
| chr4:37668269
|
G | A | 1 | a0001c0001t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.88+17931C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668269 | ||||||
| chr4:37668282
|
A | C | 1 | a0001c0001t0012g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.88+17918T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668282 | ||||||
| chr4:37668450
|
G | A | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17750C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668450 | ||||||
| chr4:37668460
|
C | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0002g0091others(2): Show | 5 | HG01516.hp2 HG01517.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+17740G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668460 | ||||||
| chr4:37668517
|
G | C | 198 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0041others(195): Show | 201 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.88+17683C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668517 | ||||||
| chr4:37668522
|
A | G | 2 | a0001c0001t0015g0251a0001c0006t0025g0252 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+17678T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668522 | ||||||
| chr4:37668551
|
G | C | 1 | a0001c0001t0036g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.88+17649C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668551 | ||||||
| chr4:37668565
|
A | C | 2 | a0001c0001t0001g0298a0001c0001t0023g0297 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.88+17635T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668565 | ||||||
| chr4:37668626
|
C | G | 2 | a0001c0001t0002g0220a0001c0001t0071g0134 | 2 | HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.88+17574G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668626 | ||||||
| chr4:37668636
|
A | AC | 5 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0003g0179others(2): Show | 5 | HG02080.hp1 HG02602.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+17563dupG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668636 | ||||||
| chr4:37668659
|
G | A | 1 | a0001c0001t0001g0088 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.88+17541C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668659 | ||||||
| chr4:37668673
|
G | A | 4 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0075g0314others(1): Show | 4 | HG02071.hp1 HG02129.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+17527C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668673 | ||||||
| chr4:37668733
|
G | A | 27 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(24): Show | 27 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.88+17467C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668733 | ||||||
| chr4:37668745
|
G | C | 1 | a0001c0001t0002g0163 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.88+17455C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668745 | ||||||
| chr4:37668745
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.88+17455C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668745 | ||||||
| chr4:37668753
|
TCCCATCT others(33): Show |
T | 33 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(30): Show | 34 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.88+17407_88+17446d others(42): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668753 | ||||||
| chr4:37668766
|
G | A | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0002g0091others(2): Show | 5 | HG01516.hp2 HG01517.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+17434C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668766 | ||||||
| chr4:37668793
|
C | T | 281 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0031others(278): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.88+17407G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668793 | ||||||
| chr4:37668800
|
T | TA | 4 | a0001c0001t0001g0117a0001c0001t0001g0219a0001c0001t0001g0227others(1): Show | 4 | HG01256.hp1 HG01361.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+17399dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668800 | ||||||
| chr4:37668813
|
G | C | 4 | a0001c0001t0013g0052a0001c0001t0013g0076a0001c0001t0013g0078others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+17387C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668813 | ||||||
| chr4:37668838
|
C | G | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17362G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668838 | ||||||
| chr4:37668845
|
G | C | 3 | a0001c0001t0010g0062a0001c0001t0010g0063a0001c0001t0027g0061 | 3 | NA18977.hp2 NA18983.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.88+17355C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668845 | ||||||
| chr4:37668852
|
G | A | 1 | a0001c0001t0005g0258 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+17348C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668852 | ||||||
| chr4:37668871
|
T | C | 116 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.88+17329A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668871 | ||||||
| chr4:37668873
|
G | A | 2 | a0001c0001t0015g0251a0001c0006t0025g0252 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+17327C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668873 | ||||||
| chr4:37668902
|
G | C | 2 | a0001c0001t0002g0220a0001c0001t0071g0134 | 2 | HG01943.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.88+17298C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668902 | ||||||
| chr4:37668958
|
GGTGAGGA others(169): Show |
G | 5 | a0001c0001t0004g0053a0001c0001t0004g0110a0001c0001t0004g0123others(2): Show | 5 | HG01361.hp1 HG03490.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+17066_88+17241d others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668958 | ||||||
| chr4:37668960
|
T | C | 1 | a0001c0001t0015g0251 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.88+17240A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668960 | ||||||
| chr4:37668986
|
G | T | 2 | a0001c0001t0015g0251a0001c0006t0025g0252 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+17214C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668986 | ||||||
| chr4:37668991
|
A | G | 101 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(98): Show | 102 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.88+17209T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668991 | ||||||
| chr4:37668995
|
A | G | 101 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(98): Show | 102 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.88+17205T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37668995 | ||||||
| chr4:37669006
|
GGGGGGGT others(41): Show |
G | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17146_88+17193d others(50): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669006 | ||||||
| chr4:37669088
|
C | T | 2 | a0001c0001t0004g0144a0001c0001t0069g0178 | 2 | HG00741.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.88+17112G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669088 | ||||||
| chr4:37669092
|
T | C | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17108A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669092 | ||||||
| chr4:37669106
|
C | A | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17094G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669106 | ||||||
| chr4:37669107
|
G | A | 2 | a0001c0001t0005g0253a0001c0001t0008g0257 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88+17093C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669107 | ||||||
| chr4:37669117
|
G | A | 66 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(63): Show | 66 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.88+17083C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669117 | ||||||
| chr4:37669119
|
C | A | 8 | a0001c0001t0004g0080a0001c0001t0004g0083a0001c0001t0004g0084others(5): Show | 8 | HG01081.hp1 HG01358.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+17081G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669119 | ||||||
| chr4:37669121
|
G | A | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17079C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669121 | ||||||
| chr4:37669121
|
GCCCCTAC others(347): Show |
G | 1 | a0001c0001t0026g0173 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.88+16725_88+17078d others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669121 | ||||||
| chr4:37669124
|
C | T | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+17076G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669124 | ||||||
| chr4:37669153
|
CGGCCAGC others(46): Show |
C | 4 | a0001c0001t0001g0237a0001c0001t0005g0253a0001c0001t0008g0257others(1): Show | 4 | HG01081.hp2 HG02055.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+16994_88+17046d others(55): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669153 | ||||||
| chr4:37669161
|
C | G | 2 | a0001c0001t0015g0251a0001c0006t0025g0252 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+17039G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669161 | ||||||
| chr4:37669166
|
C | T | 1 | a0001c0001t0005g0007 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.88+17034G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669166 | ||||||
| chr4:37669170
|
C | A | 5 | a0001c0001t0001g0267a0001c0001t0001g0268a0001c0001t0002g0269others(2): Show | 5 | NA18945.hp1 NA18950.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+17030G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669170 | ||||||
| chr4:37669170
|
C | T | 2 | a0001c0001t0016g0166a0001c0001t0053g0099 | 2 | HG01257.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.88+17030G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669170 | ||||||
| chr4:37669181
|
TG | T | 197 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0036others(194): Show | 200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.88+17018delC | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669181 | ||||||
| chr4:37669181
|
TGG | T | 63 | a0001c0001t0001g0015a0001c0001t0001g0172a0001c0001t0001g0273others(60): Show | 63 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.88+17017_88+17018d others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669181 | ||||||
| chr4:37669186
|
GGGGGGGT others(41): Show |
G | 1 | a0001c0001t0005g0020 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.88+16966_88+17013d others(50): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669186 | ||||||
| chr4:37669187
|
GGGGGGTC others(40): Show |
G | 15 | a0001c0001t0001g0024a0001c0001t0001g0249a0001c0001t0002g0009others(12): Show | 15 | HG01243.hp1 HG01255.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+16966_88+17012d others(49): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669187 | ||||||
| chr4:37669188
|
G | A | 1 | a0001c0001t0003g0238 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.88+17012C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669188 | ||||||
| chr4:37669188
|
GGGGGTCA others(39): Show |
G | 5 | a0001c0001t0001g0033a0001c0001t0008g0016a0001c0001t0012g0034others(2): Show | 5 | HG01167.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+16966_88+17011d others(48): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669188 | ||||||
| chr4:37669189
|
GGGGTCAG others(38): Show |
G | 4 | a0001c0001t0004g0075a0001c0001t0013g0052a0001c0001t0013g0076others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+16966_88+17010d others(47): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669189 | ||||||
| chr4:37669190
|
G | T | 2 | a0001c0001t0012g0141a0001c0001t0063g0289 | 2 | HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.88+17010C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669190 | ||||||
| chr4:37669190
|
GGGTCAGC others(37): Show |
G | 4 | a0001c0001t0005g0007a0001c0001t0005g0068a0001c0001t0013g0078others(1): Show | 4 | HG02257.hp2 HG02273.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+16966_88+17009d others(46): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669190 | ||||||
| chr4:37669191
|
GGTCAGCC others(36): Show |
G | 1 | a0001c0001t0008g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.88+16966_88+17008d others(45): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669191 | ||||||
| chr4:37669194
|
C | A | 1 | a0001c0001t0001g0150 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.88+17006G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669194 | ||||||
| chr4:37669218
|
C | T | 29 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(26): Show | 29 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.88+16982G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669218 | ||||||
| chr4:37669220
|
GTCCGGGA others(40): Show |
G | 1 | a0001c0001t0018g0002 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.88+16933_88+16979d others(49): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669220 | ||||||
| chr4:37669249
|
C | T | 3 | a0001c0001t0005g0068a0001c0001t0008g0069a0001c0001t0061g0050 | 3 | HG02257.hp2 HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.88+16951G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669249 | ||||||
| chr4:37669253
|
C | T | 3 | a0001c0001t0005g0068a0001c0001t0008g0069a0001c0001t0061g0050 | 3 | HG02257.hp2 HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.88+16947G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669253 | ||||||
| chr4:37669267
|
A | G | 30 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(27): Show | 30 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.88+16933T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669267 | ||||||
| chr4:37669294
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.88+16906G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669294 | ||||||
| chr4:37669298
|
C | G | 4 | a0001c0001t0005g0068a0001c0001t0008g0069a0001c0001t0018g0002others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16902G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669298 | ||||||
| chr4:37669327
|
T | C | 42 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0249others(39): Show | 42 | HG00140.hp1 HG00733.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.88+16873A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669327 | ||||||
| chr4:37669340
|
G | T | 1 | a0001c0001t0006g0104 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.88+16860C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669340 | ||||||
| chr4:37669348
|
C | T | 2 | a0001c0001t0036g0293a0001c0001t0046g0319 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.88+16852G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669348 | ||||||
| chr4:37669349
|
G | C | 1 | a0001c0001t0021g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.88+16851C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669349 | ||||||
| chr4:37669375
|
C | T | 5 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0002g0091others(2): Show | 5 | HG01516.hp2 HG01517.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16825G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669375 | ||||||
| chr4:37669378
|
C | A | 1 | a0001c0001t0007g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.88+16822G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669378 | ||||||
| chr4:37669394
|
G | A | 1 | a0001c0001t0004g0080 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.88+16806C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669394 | ||||||
| chr4:37669409
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.88+16791C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669409 | ||||||
| chr4:37669430
|
G | C | 4 | a0001c0001t0005g0068a0001c0001t0008g0069a0001c0001t0018g0002others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16770C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669430 | ||||||
| chr4:37669442
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0026g0280 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+16758G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669442 | ||||||
| chr4:37669446
|
C | T | 2 | a0001c0001t0036g0293a0001c0001t0046g0319 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.88+16754G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669446 | ||||||
| chr4:37669461
|
G | A | 4 | a0001c0001t0005g0068a0001c0001t0008g0069a0001c0001t0018g0002others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16739C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669461 | ||||||
| chr4:37669541
|
G | A | 2 | a0001c0001t0015g0251a0001c0006t0025g0252 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+16659C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669541 | ||||||
| chr4:37669561
|
G | A | 39 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(36): Show | 39 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.88+16639C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669561 | ||||||
| chr4:37669573
|
A | G | 4 | a0001c0001t0001g0226a0001c0001t0005g0224a0001c0001t0005g0225others(1): Show | 4 | HG02572.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+16627T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669573 | ||||||
| chr4:37669575
|
T | C | 4 | a0001c0001t0001g0226a0001c0001t0005g0224a0001c0001t0005g0225others(1): Show | 4 | HG02572.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+16625A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669575 | ||||||
| chr4:37669596
|
G | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0026g0280 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+16604C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669596 | ||||||
| chr4:37669634
|
G | A | 4 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0075g0314others(1): Show | 4 | HG02071.hp1 HG02129.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.88+16566C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669634 | ||||||
| chr4:37669702
|
A | G | 4 | a0001c0001t0005g0068a0001c0001t0008g0069a0001c0001t0018g0002others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16498T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669702 | ||||||
| chr4:37669706
|
T | C | 70 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(67): Show | 70 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.88+16494A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669706 | ||||||
| chr4:37669827
|
C | T | 4 | a0001c0001t0005g0068a0001c0001t0008g0069a0001c0001t0018g0002others(1): Show | 5 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+16373G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669827 | ||||||
| chr4:37669847
|
G | A | 192 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0041others(189): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.88+16353C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669847 | ||||||
| chr4:37669895
|
C | T | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0026g0280 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+16305G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669895 | ||||||
| chr4:37669897
|
A | C | 107 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(104): Show | 108 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.88+16303T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669897 | ||||||
| chr4:37669930
|
A | G | 3 | a0001c0001t0012g0291a0001c0001t0029g0290a0001c0003t0058g0292 | 3 | HG01884.hp2 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.88+16270T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669930 | ||||||
| chr4:37669934
|
A | G | 2 | a0001c0001t0043g0038a0001c0001t0044g0039 | 2 | HG01358.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.88+16266T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669934 | ||||||
| chr4:37669941
|
T | C | 2 | a0001c0001t0036g0293a0001c0001t0046g0319 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.88+16259A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37669941 | ||||||
| chr4:37670056
|
TA | T | 20 | a0001c0001t0001g0024a0001c0001t0002g0009a0001c0001t0002g0103others(17): Show | 21 | HG02071.hp1 HG02129.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.88+16143delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670056 | ||||||
| chr4:37670061
|
A | G | 1 | a0001c0001t0055g0026 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.88+16139T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670061 | ||||||
| chr4:37670100
|
A | T | 2 | a0001c0001t0007g0312a0001c0001t0033g0302 | 2 | HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.88+16100T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670100 | ||||||
| chr4:37670210
|
G | GT | 42 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0172others(39): Show | 42 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.88+15989dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670210 | ||||||
| chr4:37670242
|
G | A | 1 | a0001c0001t0004g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88+15958C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670242 | ||||||
| chr4:37670339
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.88+15861C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670339 | ||||||
| chr4:37670566
|
C | T | 1 | a0001c0001t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.88+15634G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670566 | ||||||
| chr4:37670575
|
C | CT | 31 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0193others(28): Show | 32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.88+15624dupA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670575 | ||||||
| chr4:37670767
|
T | A | 6 | a0001c0001t0005g0253a0001c0001t0008g0257a0001c0001t0048g0256others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+15433A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670767 | ||||||
| chr4:37670772
|
C | T | 19 | a0001c0001t0001g0033a0001c0001t0001g0249a0001c0001t0002g0009others(16): Show | 19 | HG01167.hp1 HG01243.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.88+15428G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670772 | ||||||
| chr4:37670789
|
A | G | 290 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(287): Show | 294 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.88+15411T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670789 | ||||||
| chr4:37670818
|
C | T | 1 | a0001c0001t0062g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+15382G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37670818 | ||||||
| chr4:37671031
|
C | G | 3 | a0001c0001t0001g0036a0001c0001t0007g0037a0001c0001t0007g0040 | 3 | HG00323.hp1 HG01123.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.88+15169G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671031 | ||||||
| chr4:37671058
|
T | C | 5 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0015g0251others(2): Show | 5 | HG01243.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+15142A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671058 | ||||||
| chr4:37671082
|
A | G | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.88+15118T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671082 | ||||||
| chr4:37671109
|
A | T | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.88+15091T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671109 | ||||||
| chr4:37671200
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.88+15000A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671200 | ||||||
| chr4:37671220
|
C | G | 26 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0185others(23): Show | 26 | HG00621.hp2 HG01257.hp1 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+14980G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671220 | ||||||
| chr4:37671253
|
C | G | 229 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0041others(226): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.88+14947G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671253 | ||||||
| chr4:37671259
|
C | T | 225 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0041others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.88+14941G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671259 | ||||||
| chr4:37671272
|
A | G | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.88+14928T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671272 | ||||||
| chr4:37671371
|
G | T | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.88+14829C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671371 | ||||||
| chr4:37671657
|
T | C | 13 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(10): Show | 13 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+14543A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671657 | ||||||
| chr4:37671723
|
G | GCTATGCC others(12): Show |
5 | a0001c0001t0001g0317a0001c0001t0002g0315a0001c0001t0002g0316others(2): Show | 5 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14476_88+14477i others(21): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671723 | ||||||
| chr4:37671724
|
G | A | 5 | a0001c0001t0001g0317a0001c0001t0002g0315a0001c0001t0002g0316others(2): Show | 5 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14476C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671724 | ||||||
| chr4:37671726
|
C | CTA | 5 | a0001c0001t0001g0317a0001c0001t0002g0315a0001c0001t0002g0316others(2): Show | 5 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+14473_88+14474i others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671726 | ||||||
| chr4:37671732
|
T | C | 2 | a0001c0001t0002g0073a0001c0001t0005g0074 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.88+14468A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671732 | ||||||
| chr4:37671773
|
TC | T | 232 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0041others(229): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.88+14426delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671773 | ||||||
| chr4:37671808
|
T | G | 1 | a0001c0001t0010g0138 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.88+14392A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671808 | ||||||
| chr4:37671933
|
T | C | 4 | a0001c0001t0001g0311a0001c0001t0002g0299a0001c0001t0002g0305others(1): Show | 4 | HG01106.hp1 HG02273.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+14267A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671933 | ||||||
| chr4:37671934
|
G | A | 2 | a0001c0001t0002g0299a0001c0001t0002g0305 | 2 | HG01106.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.88+14266C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671934 | ||||||
| chr4:37671968
|
G | T | 2 | a0001c0003t0019g0092a0001c0003t0019g0250 | 2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.88+14232C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37671968 | ||||||
| chr4:37672004
|
G | A | 218 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0041others(215): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.88+14196C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672004 | ||||||
| chr4:37672264
|
T | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.88+13936A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672264 | ||||||
| chr4:37672332
|
G | A | 2 | a0001c0001t0015g0251a0001c0006t0025g0252 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+13868C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672332 | ||||||
| chr4:37672344
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.88+13856A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672344 | ||||||
| chr4:37672541
|
C | A | 3 | a0001c0001t0037g0254a0001c0001t0048g0256a0001c0001t0049g0255 | 3 | HG02451.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.88+13659G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672541 | ||||||
| chr4:37672686
|
T | C | 1 | a0001c0001t0065g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.88+13514A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672686 | ||||||
| chr4:37672732
|
T | C | 1 | a0001c0001t0031g0148 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.88+13468A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672732 | ||||||
| chr4:37672755
|
C | T | 26 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(23): Show | 26 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.88+13445G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37672755 | ||||||
| chr4:37673048
|
A | C | 2 | a0001c0001t0002g0073a0001c0001t0005g0074 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.88+13152T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673048 | ||||||
| chr4:37673052
|
G | T | 266 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.88+13148C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673052 | ||||||
| chr4:37673172
|
T | C | 2 | a0001c0001t0005g0253a0001c0001t0008g0257 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88+13028A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673172 | ||||||
| chr4:37673175
|
A | T | 2 | a0001c0001t0015g0251a0001c0006t0025g0252 | 2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.88+13025T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673175 | ||||||
| chr4:37673186
|
C | CTT | 11 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(8): Show | 11 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+13012_88+13013d others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | ||||||
| chr4:37673186
|
C | CTTTTTT | 169 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(166): Show | 172 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.88+13008_88+13013d others(8): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | ||||||
| chr4:37673186
|
C | CTTTTTTT | 79 | a0001c0001t0001g0088a0001c0001t0001g0107a0001c0001t0001g0109others(76): Show | 80 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.88+13007_88+13013d others(9): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | ||||||
| chr4:37673186
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0002g0098a0001c0001t0003g0101a0001c0001t0006g0152others(5): Show | 8 | HG01433.hp2 HG01928.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+13006_88+13013d others(10): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | ||||||
| chr4:37673186
|
C | T | 1 | a0001c0001t0003g0139 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.88+13014G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | ||||||
| chr4:37673186
|
CT | C | 10 | a0001c0001t0001g0313a0001c0001t0002g0073a0001c0001t0002g0296others(7): Show | 10 | HG01070.hp1 HG01071.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.88+13013delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673186 | ||||||
| chr4:37673190
|
T | C | 7 | a0001c0001t0005g0253a0001c0001t0008g0257a0001c0001t0037g0254others(4): Show | 7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+13010A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673190 | ||||||
| chr4:37673213
|
A | G | 8 | a0001c0001t0002g0105a0001c0001t0002g0175a0001c0001t0003g0177others(5): Show | 8 | HG00673.hp1 HG01123.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+12987T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673213 | ||||||
| chr4:37673218
|
T | C | 307 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(304): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.88+12982A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673218 | ||||||
| chr4:37673253
|
T | C | 274 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.88+12947A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673253 | ||||||
| chr4:37673264
|
A | G | 41 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(38): Show | 41 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.88+12936T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673264 | ||||||
| chr4:37673288
|
T | C | 1 | a0001c0003t0019g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.88+12912A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673288 | ||||||
| chr4:37673389
|
G | C | 1 | a0001c0001t0003g0230 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.88+12811C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673389 | ||||||
| chr4:37673467
|
C | T | 1 | a0001c0001t0063g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.88+12733G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673467 | ||||||
| chr4:37673559
|
G | A | 18 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(15): Show | 18 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+12641C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673559 | ||||||
| chr4:37673766
|
G | A | 192 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0041others(189): Show | 195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.88+12434C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673766 | ||||||
| chr4:37673822
|
G | A | 14 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(11): Show | 14 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+12378C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37673822 | ||||||
| chr4:37674071
|
G | A | 7 | a0001c0001t0005g0253a0001c0001t0008g0257a0001c0001t0037g0254others(4): Show | 7 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+12129C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674071 | ||||||
| chr4:37674161
|
T | C | 1 | a0001c0001t0003g0155 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.88+12039A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674161 | ||||||
| chr4:37674162
|
A | C | 6 | a0001c0001t0012g0291a0001c0001t0029g0290a0001c0001t0036g0293others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+12038T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674162 | ||||||
| chr4:37674269
|
C | T | 2 | a0001c0001t0003g0151a0001c0001t0074g0093 | 2 | HG00558.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.88+11931G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674269 | ||||||
| chr4:37674319
|
A | C | 274 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.88+11881T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674319 | ||||||
| chr4:37674540
|
G | A | 274 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.88+11660C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674540 | ||||||
| chr4:37674556
|
A | C | 274 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.88+11644T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674556 | ||||||
| chr4:37674629
|
G | A | 7 | a0001c0001t0002g0073a0001c0001t0004g0075a0001c0001t0005g0074others(4): Show | 7 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+11571C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674629 | ||||||
| chr4:37674746
|
GC | G | 274 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(271): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.88+11453delG | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674746 | ||||||
| chr4:37674759
|
T | C | 1 | a0001c0001t0005g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.88+11441A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37674759 | ||||||
| chr4:37675348
|
T | C | 2 | a0001c0001t0004g0231a0001c0001t0004g0232 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.88+10852A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675348 | ||||||
| chr4:37675471
|
T | C | 60 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(57): Show | 60 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.88+10729A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675471 | ||||||
| chr4:37675705
|
C | T | 8 | a0001c0001t0002g0103a0001c0001t0003g0101a0001c0001t0003g0168others(5): Show | 8 | HG00621.hp2 HG02074.hp2 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+10495G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675705 | ||||||
| chr4:37675886
|
T | C | 2 | a0001c0001t0008g0069a0001c0001t0061g0050 | 2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.88+10314A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675886 | ||||||
| chr4:37675932
|
C | G | 1 | a0001c0001t0005g0014 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.88+10268G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675932 | ||||||
| chr4:37675978
|
T | C | 1 | a0001c0001t0060g0070 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.88+10222A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37675978 | ||||||
| chr4:37676196
|
C | G | 1 | a0001c0001t0004g0085 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.88+10004G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676196 | ||||||
| chr4:37676357
|
C | T | 39 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(36): Show | 39 | HG00408.hp2 HG00423.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.88+9843G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676357 | ||||||
| chr4:37676442
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.88+9758C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676442 | ||||||
| chr4:37676516
|
C | T | 59 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(56): Show | 59 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.88+9684G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676516 | ||||||
| chr4:37676846
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.88+9354G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676846 | ||||||
| chr4:37676872
|
T | C | 32 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(29): Show | 32 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.88+9328A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676872 | ||||||
| chr4:37676885
|
C | T | 32 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(29): Show | 32 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.88+9315G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676885 | ||||||
| chr4:37676919
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.88+9281C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37676919 | ||||||
| chr4:37677005
|
C | T | 1 | a0001c0001t0015g0071 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.88+9195G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677005 | ||||||
| chr4:37677182
|
A | T | 4 | a0001c0001t0002g0098a0001c0001t0016g0100a0001c0001t0016g0166others(1): Show | 4 | HG01257.hp1 HG01928.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+9018T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677182 | ||||||
| chr4:37677268
|
T | C | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.88+8932A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677268 | ||||||
| chr4:37677343
|
C | T | 8 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+8857G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677343 | ||||||
| chr4:37677650
|
C | T | 52 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(49): Show | 52 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.88+8550G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677650 | ||||||
| chr4:37677832
|
C | T | 1 | a0001c0001t0004g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.88+8368G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677832 | ||||||
| chr4:37677921
|
G | A | 5 | a0001c0001t0001g0150a0001c0001t0001g0233a0001c0001t0003g0139others(2): Show | 5 | NA18941.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+8279C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37677921 | ||||||
| chr4:37678049
|
G | A | 1 | a0001c0001t0006g0235 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.88+8151C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678049 | ||||||
| chr4:37678122
|
AGAGGAGC others(8): Show |
A | 6 | a0001c0001t0005g0253a0001c0001t0008g0257a0001c0001t0037g0254others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+8063_88+8077del others(15): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678122 | ||||||
| chr4:37678135
|
C | T | 1 | a0001c0001t0001g0278 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.88+8065G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678135 | ||||||
| chr4:37678145
|
C | T | 2 | a0001c0001t0032g0097a0001c0001t0070g0164 | 2 | NA18942.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.88+8055G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678145 | ||||||
| chr4:37678146
|
G | A | 25 | a0001c0001t0001g0140a0001c0001t0001g0236a0001c0001t0001g0237others(22): Show | 25 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.88+8054C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678146 | ||||||
| chr4:37678166
|
G | C | 1 | a0001c0001t0017g0049 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.88+8034C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678166 | ||||||
| chr4:37678170
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0004g0030others(2): Show | 5 | HG00642.hp2 HG01099.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+8030C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678170 | ||||||
| chr4:37678249
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.88+7951T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678249 | ||||||
| chr4:37678255
|
C | T | 18 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(15): Show | 18 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+7945G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678255 | ||||||
| chr4:37678372
|
A | G | 20 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(17): Show | 20 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+7828T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678372 | ||||||
| chr4:37678482
|
A | G | 20 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(17): Show | 20 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.88+7718T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678482 | ||||||
| chr4:37678491
|
T | G | 3 | a0001c0001t0001g0033a0001c0001t0005g0032a0001c0001t0028g0012 | 3 | HG01243.hp1 HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.88+7709A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678491 | ||||||
| chr4:37678601
|
A | T | 1 | a0001c0001t0004g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.88+7599T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678601 | ||||||
| chr4:37678705
|
T | A | 1 | a0001c0001t0050g0013 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.88+7495A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678705 | ||||||
| chr4:37678707
|
T | C | 1 | a0001c0001t0012g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.88+7493A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678707 | ||||||
| chr4:37678735
|
C | G | 2 | a0001c0001t0002g0299a0001c0001t0002g0305 | 2 | HG01106.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.88+7465G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678735 | ||||||
| chr4:37678762
|
C | T | 262 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(259): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.88+7438G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678762 | ||||||
| chr4:37678933
|
A | T | 6 | a0001c0001t0002g0096a0001c0001t0002g0159a0001c0001t0002g0162others(3): Show | 6 | HG02080.hp1 NA18946.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+7267T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37678933 | ||||||
| chr4:37679099
|
A | G | 2 | a0001c0001t0006g0157a0001c0001t0023g0095 | 2 | HG03654.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.88+7101T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679099 | ||||||
| chr4:37679171
|
AAG | A | 3 | a0001c0001t0003g0051a0001c0001t0003g0072a0001c0001t0015g0071 | 3 | HG01928.hp2 HG01975.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.88+7027_88+7028del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679171 | ||||||
| chr4:37679240
|
G | A | 18 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(15): Show | 18 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.88+6960C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679240 | ||||||
| chr4:37679307
|
T | G | 1 | a0001c0001t0006g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.88+6893A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679307 | ||||||
| chr4:37679466
|
A | G | 1 | a0001c0006t0025g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.88+6734T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679466 | ||||||
| chr4:37679568
|
A | G | 14 | a0001c0001t0001g0041a0001c0001t0001g0081a0001c0001t0001g0082others(11): Show | 14 | HG00140.hp2 HG01081.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+6632T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679568 | ||||||
| chr4:37679574
|
C | T | 3 | a0001c0001t0002g0296a0001c0001t0004g0295a0001c0001t0014g0294 | 3 | HG02056.hp1 HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.88+6626G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679574 | ||||||
| chr4:37679664
|
C | G | 1 | a0001c0001t0054g0263 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.88+6536G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679664 | ||||||
| chr4:37679665
|
A | T | 19 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(16): Show | 19 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+6535T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679665 | ||||||
| chr4:37679884
|
G | A | 3 | a0001c0001t0037g0254a0001c0001t0048g0256a0001c0001t0049g0255 | 3 | HG02451.hp2 HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.88+6316C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679884 | ||||||
| chr4:37679893
|
A | T | 2 | a0001c0001t0005g0253a0001c0001t0008g0257 | 2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.88+6307T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679893 | ||||||
| chr4:37679972
|
C | T | 4 | a0001c0001t0004g0084a0001c0001t0012g0291a0001c0001t0029g0290others(1): Show | 4 | HG01884.hp2 HG03017.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.88+6228G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37679972 | ||||||
| chr4:37680082
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.88+6118T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680082 | ||||||
| chr4:37680104
|
A | T | 1 | a0001c0001t0002g0042 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.88+6096T>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680104 | ||||||
| chr4:37680188
|
C | T | 19 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(16): Show | 19 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+6012G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680188 | ||||||
| chr4:37680301
|
C | G | 1 | a0001c0001t0006g0157 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.88+5899G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680301 | ||||||
| chr4:37680457
|
C | T | 25 | a0001c0001t0001g0249a0001c0001t0003g0051a0001c0001t0003g0072others(22): Show | 27 | HG00099.hp1 HG01167.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.88+5743G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680457 | ||||||
| chr4:37680638
|
G | A | 1 | a0001c0001t0064g0240 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.88+5562C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680638 | ||||||
| chr4:37680744
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.88+5456G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680744 | ||||||
| chr4:37680837
|
C | T | 1 | a0001c0006t0025g0252 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.88+5363G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680837 | ||||||
| chr4:37680843
|
A | G | 18 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(15): Show | 18 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.88+5357T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680843 | ||||||
| chr4:37680848
|
C | T | 1 | a0001c0001t0017g0049 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.88+5352G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680848 | ||||||
| chr4:37680886
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.88+5314G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680886 | ||||||
| chr4:37680931
|
C | CA | 16 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0243others(13): Show | 16 | HG00323.hp2 HG00741.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+5268dupT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | ||||||
| chr4:37680931
|
C | CAA | 17 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0311others(14): Show | 17 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.88+5267_88+5268dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | ||||||
| chr4:37680931
|
CA | C | 52 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0033others(49): Show | 53 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.88+5268delT | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | ||||||
| chr4:37680931
|
CAA | C | 16 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0003g0051others(13): Show | 16 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.88+5267_88+5268del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | ||||||
| chr4:37680931
|
CAAA | C | 27 | a0001c0001t0001g0249a0001c0001t0002g0073a0001c0001t0003g0072others(24): Show | 29 | HG00099.hp1 HG01167.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.88+5266_88+5268del others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | ||||||
| chr4:37680931
|
CAAAA | C | 11 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(8): Show | 11 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.88+5265_88+5268del others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37680931 | ||||||
| chr4:37681142
|
T | C | 19 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(16): Show | 19 | HG00140.hp1 HG00597.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.88+5058A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681142 | ||||||
| chr4:37681377
|
C | G | 2 | a0003c0004t0035g0005a0003c0004t0045g0006 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.88+4823G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681377 | ||||||
| chr4:37681394
|
A | G | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.88+4806T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681394 | ||||||
| chr4:37681400
|
T | G | 2 | a0001c0001t0004g0053a0001c0001t0004g0245 | 2 | HG03688.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.88+4800A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681400 | ||||||
| chr4:37681477
|
G | A | 1 | a0001c0001t0004g0246 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.88+4723C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681477 | ||||||
| chr4:37681518
|
GT | G | 168 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0031others(165): Show | 171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.88+4681delA | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | ||||||
| chr4:37681518
|
GTT | G | 20 | a0001c0001t0001g0088a0001c0001t0001g0267a0001c0001t0001g0268others(17): Show | 20 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.88+4680_88+4681del others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | ||||||
| chr4:37681518
|
GTTT | G | 7 | a0001c0001t0001g0298a0001c0001t0002g0299a0001c0001t0002g0300others(4): Show | 7 | HG00423.hp2 HG01106.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+4679_88+4681del others(3): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | ||||||
| chr4:37681518
|
GTTTT | G | 20 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0311others(17): Show | 20 | HG00408.hp2 HG02055.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.88+4678_88+4681del others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | ||||||
| chr4:37681518
|
GTTTTT | G | 7 | a0001c0001t0001g0317a0001c0001t0002g0315a0001c0001t0002g0316others(4): Show | 7 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+4677_88+4681del others(5): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681518 | ||||||
| chr4:37681522
|
T | G | 5 | a0001c0001t0001g0298a0001c0001t0002g0299a0001c0001t0002g0300others(2): Show | 5 | HG00423.hp2 HG01106.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+4678A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681522 | ||||||
| chr4:37681523
|
T | G | 20 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0311others(17): Show | 20 | HG00408.hp2 HG02055.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.88+4677A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681523 | ||||||
| chr4:37681524
|
T | G | 7 | a0001c0001t0001g0317a0001c0001t0002g0315a0001c0001t0002g0316others(4): Show | 7 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+4676A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681524 | ||||||
| chr4:37681533
|
T | G | 5 | a0001c0001t0001g0317a0001c0001t0002g0315a0001c0001t0002g0316others(2): Show | 5 | HG02040.hp1 HG02071.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+4667A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681533 | ||||||
| chr4:37681688
|
C | T | 26 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(23): Show | 26 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+4512G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681688 | ||||||
| chr4:37681991
|
T | C | 1 | a0001c0001t0027g0247 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.88+4209A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37681991 | ||||||
| chr4:37682133
|
A | C | 314 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(311): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.88+4067T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682133 | ||||||
| chr4:37682663
|
T | C | 1 | a0001c0001t0006g0318 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.88+3537A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682663 | ||||||
| chr4:37682704
|
C | T | 23 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(20): Show | 23 | HG00140.hp1 HG00597.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.88+3496G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682704 | ||||||
| chr4:37682807
|
G | A | 1 | a0001c0001t0005g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.88+3393C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682807 | ||||||
| chr4:37682843
|
A | C | 23 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(20): Show | 23 | HG00140.hp1 HG00597.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.88+3357T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37682843 | ||||||
| chr4:37683224
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.88+2976C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683224 | ||||||
| chr4:37683248
|
A | C | 6 | a0001c0001t0005g0253a0001c0001t0008g0257a0001c0001t0037g0254others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+2952T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683248 | ||||||
| chr4:37683274
|
G | A | 170 | a0001c0001t0001g0004a0001c0001t0001g0036a0001c0001t0001g0043others(167): Show | 172 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.88+2926C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683274 | ||||||
| chr4:37683446
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.88+2754A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683446 | ||||||
| chr4:37683856
|
C | T | 1 | a0001c0001t0062g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.88+2344G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683856 | ||||||
| chr4:37683858
|
G | T | 2 | a0001c0001t0001g0046a0001c0001t0004g0047 | 2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.88+2342C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683858 | ||||||
| chr4:37683974
|
T | G | 5 | a0001c0001t0012g0291a0001c0001t0029g0290a0001c0001t0036g0293others(2): Show | 5 | HG01884.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+2226A>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37683974 | ||||||
| chr4:37684016
|
G | A | 6 | a0001c0001t0012g0291a0001c0001t0029g0290a0001c0001t0036g0293others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+2184C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684016 | ||||||
| chr4:37684032
|
C | T | 3 | a0001c0001t0002g0296a0001c0001t0004g0295a0001c0001t0014g0294 | 3 | HG02056.hp1 HG02698.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.88+2168G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684032 | ||||||
| chr4:37684055
|
G | A | 46 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(43): Show | 46 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.88+2145C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684055 | ||||||
| chr4:37684349
|
C | CAA | 8 | a0001c0001t0005g0253a0001c0001t0005g0258a0001c0001t0008g0257others(5): Show | 8 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+1849_88+1850dup others(2): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684349 | ||||||
| chr4:37684349
|
C | CAAAA | 7 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0001g0276others(4): Show | 7 | HG02257.hp1 HG02523.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.88+1847_88+1850dup others(4): Show |
RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684349 | ||||||
| chr4:37684473
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.88+1727G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684473 | ||||||
| chr4:37684488
|
T | C | 8 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.88+1712A>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684488 | ||||||
| chr4:37684647
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.88+1553C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684647 | ||||||
| chr4:37684654
|
G | A | 13 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(10): Show | 13 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+1546C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37684654 | ||||||
| chr4:37685264
|
G | C | 308 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(305): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.88+936C>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685264 | ||||||
| chr4:37685316
|
A | G | 1 | a0001c0001t0073g0044 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.88+884T>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685316 | ||||||
| chr4:37685473
|
G | T | 2 | a0001c0001t0001g0273a0001c0001t0066g0272 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.88+727C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685473 | ||||||
| chr4:37685508
|
C | A | 13 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0268others(10): Show | 13 | HG00140.hp1 HG00597.hp2 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+692G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685508 | ||||||
| chr4:37685611
|
G | A | 10 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+589C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685611 | ||||||
| chr4:37685719
|
A | C | 2 | a0001c0001t0001g0043a0001c0001t0002g0042 | 2 | HG02080.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.88+481T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685719 | ||||||
| chr4:37685774
|
A | C | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0026g0280 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+426T>G | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685774 | ||||||
| chr4:37685787
|
AGC | A | 3 | a0001c0001t0001g0281a0001c0001t0001g0282a0001c0001t0026g0280 | 3 | HG02818.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.88+411_88+412delGC | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685787 | ||||||
| chr4:37685887
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.88+313C>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685887 | ||||||
| chr4:37685925
|
C | T | 34 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0031others(31): Show | 34 | HG00323.hp1 HG00642.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.88+275G>A | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685925 | ||||||
| chr4:37685931
|
T | A | 308 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(305): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.88+269A>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685931 | ||||||
| chr4:37685938
|
C | G | 308 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0024others(305): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.88+262G>C | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37685938 | ||||||
| chr4:37686032
|
C | A | 26 | a0001c0001t0001g0298a0001c0001t0001g0306a0001c0001t0001g0308others(23): Show | 26 | HG00408.hp2 HG00423.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.88+168G>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37686032 | ||||||
| chr4:37686190
|
G | A | 1 | a0001c0001t0046g0319 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88+10C>T | RELL1 | ENSG00000181826.10 | transcript | ENST00000454158.7 | protein_coding | 1/6 | chr4 | 37686190 |