Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55758 |
|---|---|
| ensemblid | ENSG00000117625.14 |
| hgncid | 25594 |
| symbol | RCOR3 |
| name | REST corepressor 3 |
| refseq_nuc | NM_001136223.3 |
| refseq_prot | NP_001129695.1 |
| ensembl_nuc | ENST00000419091.7 |
| ensembl_prot | ENSP00000413929.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 211259366 |
| end | 211316385 |
| strand | + |
| ver | v1.2 |
| region | chr1:211259366-211316385 |
| region5000 | chr1:211254366-211321385 |
| regionname0 | RCOR3_chr1_211259366_211316385 |
| regionname5000 | RCOR3_chr1_211254366_211321385 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 553 | 324 | 84 | 54 | 134 | 10 | 40 | 108 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1662 | 267 | 65 | 42 | 115 | 9 | 35 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| c0002 | 0/1 | 1662 | 44 | 7 | 12 | 18 | 1 | 5 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| c0003 | 0/0 | 1662 | 10 | 10 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| c0004 | 0/0 | 1662 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| c0005 | 0/0 | 1662 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2813 | 148 | 41 | 23 | 68 | 1 | 14 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0002 | 0/0 | 2812 | 104 | 11 | 20 | 54 | 5 | 14 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0003 | 0/0 | 2814 | 16 | 0 | 3 | 6 | 1 | 6 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0004 | 0/0 | 2813 | 13 | 12 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0005 | 1/0 | 2813 | 13 | 7 | 1 | 0 | 2 | 2 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0006 | 0/0 | 2816 | 6 | 0 | 4 | 0 | 1 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0007 | 0/0 | 2813 | 5 | 5 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0008 | 0/0 | 2813 | 4 | 4 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0009 | 0/0 | 2815 | 3 | 0 | 0 | 0 | 0 | 3 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0010 | 0/0 | 2812 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0011 | 0/0 | 2813 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0012 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0013 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0014 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0015 | 0/0 | 2813 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0016 | 0/0 | 2813 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0017 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0018 | 0/0 | 2813 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| t0019 | 0/0 | 2813 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1662 | 267 | 65 | 42 | 115 | 9 | 35 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0002 | 0/1 | 1662 | 44 | 7 | 12 | 18 | 1 | 5 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0003 | 0/0 | 1662 | 10 | 10 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0004 | 0/0 | 1662 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0005 | 0/0 | 1662 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4474 | 98 | 23 | 15 | 49 | 1 | 10 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0002 | 0/0 | 4473 | 104 | 11 | 20 | 54 | 5 | 14 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0003 | 0/0 | 4475 | 16 | 0 | 3 | 6 | 1 | 6 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0004 | 0/0 | 4474 | 13 | 12 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0005 | 1/0 | 4474 | 13 | 7 | 1 | 0 | 2 | 2 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0007 | 0/0 | 4474 | 5 | 5 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0008 | 0/0 | 4474 | 4 | 4 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0009 | 0/0 | 4476 | 3 | 0 | 0 | 0 | 0 | 3 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0010 | 0/0 | 4473 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0011 | 0/0 | 4474 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0012 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0013 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0014 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0015 | 0/0 | 4474 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0016 | 0/0 | 4474 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0018 | 0/0 | 4474 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0001t0019 | 0/0 | 4474 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0002t0001 | 0/1 | 4474 | 37 | 6 | 8 | 18 | 0 | 4 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0002t0006 | 0/0 | 4477 | 6 | 0 | 4 | 0 | 1 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0002t0017 | 0/0 | 4474 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0003t0001 | 0/0 | 4474 | 10 | 10 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0004t0001 | 0/0 | 4474 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| a0001c0005t0001 | 0/0 | 4474 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | copy fasta | chr1 | 211254366 | 211321385 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0071 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0007g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0008g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0009g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0009g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0011g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0012g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0013g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0014g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0015g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0016g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0001t0019g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0006g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0006g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0006g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0002t0017g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0004t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0004t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| a0001c0005t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | GBR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | GBR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00597 | hp2 | a0001 | c0001 | t0012 | g0117 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00673 | hp1 | a0001 | c0005 | t0001 | g0061 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00738 | hp2 | a0001 | c0002 | t0006 | g0135 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01069 | hp1 | a0001 | c0001 | t0013 | g0146 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01099 | hp1 | a0001 | c0002 | t0006 | g0126 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01167 | hp2 | a0001 | c0002 | t0006 | g0196 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01256 | hp1 | a0001 | c0001 | t0014 | g0152 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0210 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | IBS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0005 | EUR | IBS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0005 | EUR | IBS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0155 | EUR | IBS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0222 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | CDX | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0208 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02293 | hp2 | a0001 | c0002 | t0006 | g0197 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0072 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0265 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0279 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02698 | hp1 | a0001 | c0002 | t0006 | g0202 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0132 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0274 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0214 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0277 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0074 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0278 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0276 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0077 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0221 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0199 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0296 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03130 | hp1 | a0001 | c0004 | t0001 | g0298 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0075 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0266 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0275 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0299 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03225 | hp2 | a0001 | c0002 | t0017 | g0128 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03453 | hp2 | a0001 | c0001 | t0018 | g0022 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0300 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03688 | hp2 | a0001 | c0001 | t0009 | g0233 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0194 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03710 | hp2 | a0001 | c0001 | t0005 | g0295 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0259 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0239 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0248 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0231 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | CHB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | CHB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | YRI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0130 | AFR | YRI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18986 | hp2 | a0001 | c0001 | t0016 | g0236 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18995 | hp1 | a0001 | c0001 | t0010 | g0095 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19004 | hp2 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | LWK | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | LWK | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19043 | hp2 | a0001 | c0001 | t0011 | g0076 | AFR | LWK | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19091 | hp1 | a0001 | c0001 | t0015 | g0177 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19091 | hp2 | a0001 | c0001 | t0019 | g0003 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19240 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | YRI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0073 | AFR | YRI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0230 | EUR | TSI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | TSI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | TSI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA20805 | hp2 | a0001 | c0002 | t0006 | g0213 | EUR | TSI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0232 | SAS | GIH | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | GIH | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0129 | AFR | USA | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | USA | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | USA | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0085 | REF | REF | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0071 | REF | REF | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:211259566
|
C | T | 1 | a0001c0003 | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
synonymous_variant | LOW | c.6C>T | p.Pro2Pro | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/12 | 201/4474 | 6/1662 | 2/553 | chr1 | 211259566 | ||
| chr1:211278125
|
T | C | 2 | a0001c0002a0001c0003 | 54 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(51): Show |
synonymous_variant | LOW | c.525T>C | p.Asp175Asp | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/12 | 720/4474 | 525/1662 | 175/553 | chr1 | 211278125 | ||
| chr1:211289306
|
G | A | 1 | a0001c0004 | 2 | HG03130.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.849G>A | p.Gln283Gln | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/12 | 1044/4474 | 849/1662 | 283/553 | chr1 | 211289306 | ||
| chr1:211313702
|
G | A | 1 | a0001c0005 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.1596G>A | p.Thr532Thr | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1791/4474 | 1596/1662 | 532/553 | chr1 | 211313702 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:211259456
|
T | TCTC | 1 | a0001c0002t0006 | 6 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-90_-88dupCCT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/12 | 87 | INFO_REALIGN_3_PRIME | chr1 | 211259456 | ||||
| chr1:211313952
|
T | A | 1 | a0001c0001t0010 | 2 | NA18995.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*184T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 184 | chr1 | 211313952 | |||||
| chr1:211314005
|
GT | G | 6 | a0001c0001t0002a0001c0001t0010a0001c0001t0012others(3): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*239delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 239 | INFO_REALIGN_3_PRIME | chr1 | 211314005 | ||||
| chr1:211314087
|
T | C | 1 | a0001c0001t0004 | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*319T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 319 | chr1 | 211314087 | |||||
| chr1:211314173
|
T | TA | 1 | a0001c0001t0009 | 3 | HG03688.hp2 HG04204.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*405_*406insA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 406 | chr1 | 211314173 | |||||
| chr1:211314212
|
T | G | 1 | a0001c0001t0011 | 2 | HG02970.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*444T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 444 | chr1 | 211314212 | |||||
| chr1:211314259
|
C | T | 1 | a0001c0001t0019 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 491 | chr1 | 211314259 | |||||
| chr1:211314261
|
G | A | 1 | a0001c0001t0016 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*493G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 493 | chr1 | 211314261 | |||||
| chr1:211314334
|
C | CT | 3 | a0001c0001t0003a0001c0001t0009a0001c0001t0015 | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*576dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 577 | INFO_REALIGN_3_PRIME | chr1 | 211314334 | ||||
| chr1:211314552
|
T | G | 1 | a0001c0002t0017 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*784T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 784 | chr1 | 211314552 | |||||
| chr1:211314734
|
A | G | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | 311 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*966A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 966 | chr1 | 211314734 | |||||
| chr1:211315196
|
C | A | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*1428C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1428 | chr1 | 211315196 | |||||
| chr1:211315376
|
A | G | 1 | a0001c0001t0014 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1608A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1608 | chr1 | 211315376 | |||||
| chr1:211315392
|
A | G | 1 | a0001c0001t0018 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1624A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1624 | chr1 | 211315392 | |||||
| chr1:211315427
|
T | C | 1 | a0001c0001t0012 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1659T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1659 | chr1 | 211315427 | |||||
| chr1:211315635
|
G | A | 1 | a0001c0001t0008 | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1867G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1867 | chr1 | 211315635 | |||||
| chr1:211315845
|
T | G | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*2077T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 2077 | chr1 | 211315845 | |||||
| chr1:211315861
|
A | C | 1 | a0001c0001t0013 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 2093 | chr1 | 211315861 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:211259891
|
C | A | 1 | a0001c0001t0001g0017 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.166+165C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/11 | chr1 | 211259891 | ||||||
| chr1:211259924
|
G | GC | 13 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(10): Show | 14 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.167-175dupC | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 211259924 | |||||
| chr1:211260078
|
T | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 56 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.167-30T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/11 | chr1 | 211260078 | ||||||
| chr1:211260268
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+104T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260268 | ||||||
| chr1:211260330
|
C | T | 47 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(44): Show | 49 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.223+166C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260330 | ||||||
| chr1:211260371
|
C | G | 1 | a0001c0001t0001g0070 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.223+207C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260371 | ||||||
| chr1:211260395
|
G | T | 290 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(287): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.223+231G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260395 | ||||||
| chr1:211260411
|
G | A | 290 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(287): Show | 306 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.223+247G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260411 | ||||||
| chr1:211260481
|
C | T | 1 | a0001c0001t0004g0301 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.223+317C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260481 | ||||||
| chr1:211260616
|
G | A | 1 | a0001c0001t0002g0079 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.223+452G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260616 | ||||||
| chr1:211260631
|
G | C | 1 | a0001c0002t0001g0080 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.223+467G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260631 | ||||||
| chr1:211260640
|
C | T | 1 | a0001c0001t0004g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.223+476C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260640 | ||||||
| chr1:211260692
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.223+528G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260692 | ||||||
| chr1:211260699
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.223+535T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260699 | ||||||
| chr1:211260751
|
G | A | 1 | a0001c0001t0005g0259 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.223+587G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260751 | ||||||
| chr1:211260754
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+590G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260754 | ||||||
| chr1:211260922
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.223+758C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260922 | ||||||
| chr1:211261042
|
C | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.223+878C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261042 | ||||||
| chr1:211261124
|
A | G | 1 | a0001c0001t0005g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.223+960A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261124 | ||||||
| chr1:211261135
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+971G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261135 | ||||||
| chr1:211261245
|
G | T | 2 | a0001c0001t0011g0076a0001c0001t0011g0077 | 2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.223+1081G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261245 | ||||||
| chr1:211261296
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+1132T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261296 | ||||||
| chr1:211261341
|
A | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.223+1177A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261341 | ||||||
| chr1:211261350
|
G | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 52 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.223+1186G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261350 | ||||||
| chr1:211261825
|
G | T | 1 | a0001c0001t0002g0249 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.223+1661G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261825 | ||||||
| chr1:211261919
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA18959.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.223+1755A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261919 | ||||||
| chr1:211261923
|
C | CAAAAAAA | 33 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0029others(30): Show | 35 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.223+1771_223+1777d others(9): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | |||||
| chr1:211261923
|
C | CAAAAAAA others(1): Show |
142 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(139): Show | 153 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.223+1770_223+1777d others(10): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | |||||
| chr1:211261923
|
C | CAAAAAAA others(2): Show |
85 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0020others(82): Show | 87 | HG00597.hp2 HG00642.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.223+1769_223+1777d others(11): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | |||||
| chr1:211261923
|
C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0002t0001g0084others(1): Show | 4 | HG06807.hp1 NA18970.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+1768_223+1777d others(12): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | |||||
| chr1:211261923
|
C | CAAAAAAA others(8): Show |
1 | a0001c0002t0001g0083 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223+1763_223+1777d others(17): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | |||||
| chr1:211261931
|
A | AAAAAAAC | 16 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(13): Show | 17 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.223+1773_223+1774i others(9): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261931 | |||||
| chr1:211261978
|
T | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.223+1814T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261978 | ||||||
| chr1:211261997
|
G | A | 52 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0024others(49): Show | 54 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.223+1833G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261997 | ||||||
| chr1:211262005
|
T | G | 1 | a0001c0001t0004g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.223+1841T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262005 | ||||||
| chr1:211262022
|
A | T | 3 | a0001c0001t0002g0125a0001c0001t0002g0194a0001c0001t0002g0195 | 3 | HG01516.hp1 HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.223+1858A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262022 | ||||||
| chr1:211262033
|
C | CTT | 6 | a0001c0001t0001g0027a0001c0001t0001g0251a0001c0001t0001g0253others(3): Show | 6 | HG01243.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+1890_223+1891d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | |||||
| chr1:211262033
|
C | CTTT | 49 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0028others(46): Show | 51 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.223+1889_223+1891d others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | |||||
| chr1:211262033
|
C | CTTTT | 95 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 101 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.223+1888_223+1891d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | |||||
| chr1:211262033
|
C | CTTTTT | 107 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0041others(104): Show | 115 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.223+1887_223+1891d others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | |||||
| chr1:211262033
|
C | CTTTTTT | 28 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0272others(25): Show | 28 | HG00597.hp2 HG01081.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.223+1886_223+1891d others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | |||||
| chr1:211262130
|
C | T | 2 | a0001c0001t0007g0002a0001c0001t0007g0075 | 5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1966C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262130 | ||||||
| chr1:211262145
|
G | C | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.223+1981G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262145 | ||||||
| chr1:211262152
|
C | T | 52 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0024others(49): Show | 54 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.223+1988C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262152 | ||||||
| chr1:211262182
|
C | T | 1 | a0001c0002t0001g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223+2018C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262182 | ||||||
| chr1:211262317
|
G | A | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.223+2153G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262317 | ||||||
| chr1:211262409
|
G | T | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+2245G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262409 | ||||||
| chr1:211262473
|
CTG | C | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+2314_223+2315d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262473 | |||||
| chr1:211262663
|
G | T | 1 | a0001c0001t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.223+2499G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262663 | ||||||
| chr1:211262676
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.223+2512C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262676 | ||||||
| chr1:211262722
|
G | A | 2 | a0001c0001t0002g0149a0001c0001t0002g0165 | 2 | HG01433.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.223+2558G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262722 | ||||||
| chr1:211262815
|
G | C | 1 | a0001c0002t0001g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.223+2651G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262815 | ||||||
| chr1:211262817
|
C | T | 1 | a0001c0003t0001g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.223+2653C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262817 | ||||||
| chr1:211262822
|
G | GT | 213 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0029others(210): Show | 225 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.223+2671dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262822 | |||||
| chr1:211262822
|
G | GTT | 72 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(69): Show | 76 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.223+2670_223+2671d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262822 | |||||
| chr1:211262870
|
C | CT | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+2717dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262870 | |||||
| chr1:211262870
|
CT | C | 120 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(117): Show | 128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.223+2717delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262870 | |||||
| chr1:211262938
|
T | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 22 | HG00609.hp1 HG01099.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+2774T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262938 | ||||||
| chr1:211263016
|
T | TC | 8 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0070others(5): Show | 8 | HG01175.hp1 HG01261.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.223+2858dupC | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263016 | |||||
| chr1:211263024
|
G | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.223+2860G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263024 | ||||||
| chr1:211263031
|
C | T | 1 | a0001c0001t0004g0266 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.223+2867C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263031 | ||||||
| chr1:211263039
|
C | T | 1 | a0001c0002t0001g0222 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.223+2875C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263039 | ||||||
| chr1:211263098
|
C | T | 15 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(12): Show | 15 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.223+2934C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263098 | ||||||
| chr1:211263141
|
C | T | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+2977C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263141 | ||||||
| chr1:211263277
|
G | C | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+3113G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263277 | ||||||
| chr1:211263399
|
T | A | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.223+3235T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263399 | ||||||
| chr1:211263428
|
AATTT | A | 77 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(74): Show | 84 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.223+3270_223+3273d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263428 | |||||
| chr1:211263432
|
T | C | 79 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(76): Show | 82 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.223+3268T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263432 | ||||||
| chr1:211263444
|
C | CTG | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.223+3281_223+3282i others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263444 | |||||
| chr1:211263641
|
T | C | 2 | a0001c0004t0001g0298a0001c0004t0001g0299 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.223+3477T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263641 | ||||||
| chr1:211263820
|
GT | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(284): Show | 303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.223+3666delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263820 | |||||
| chr1:211263826
|
T | G | 2 | a0001c0001t0001g0281a0001c0001t0002g0087 | 2 | HG01358.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.223+3662T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263826 | ||||||
| chr1:211263855
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.223+3691C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263855 | ||||||
| chr1:211263956
|
T | TACAG | 17 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(14): Show | 17 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.223+3793_223+3796d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263956 | |||||
| chr1:211264132
|
T | C | 2 | a0001c0001t0003g0234a0001c0001t0004g0261 | 2 | HG03471.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.223+3968T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264132 | ||||||
| chr1:211264214
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+4050C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264214 | ||||||
| chr1:211264364
|
G | A | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+4200G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264364 | ||||||
| chr1:211264371
|
A | G | 6 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0254others(3): Show | 6 | HG02280.hp1 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+4207A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264371 | ||||||
| chr1:211264434
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.223+4270C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264434 | ||||||
| chr1:211264461
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0251others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+4297C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264461 | ||||||
| chr1:211264518
|
C | CA | 79 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(76): Show | 82 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.223+4360dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211264518 | |||||
| chr1:211264838
|
T | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0049others(1): Show | 4 | HG00558.hp1 NA18950.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+4674T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264838 | ||||||
| chr1:211264849
|
T | C | 2 | a0001c0004t0001g0298a0001c0004t0001g0299 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.223+4685T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264849 | ||||||
| chr1:211264870
|
G | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.223+4706G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264870 | ||||||
| chr1:211265096
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.223+4932C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265096 | ||||||
| chr1:211265139
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.223+4975G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265139 | ||||||
| chr1:211265184
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+5020T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265184 | ||||||
| chr1:211265238
|
T | A | 2 | a0001c0001t0003g0235a0001c0001t0003g0247 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.223+5074T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265238 | ||||||
| chr1:211265262
|
TTAAATA | T | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+5105_223+5110d others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211265262 | |||||
| chr1:211265338
|
T | G | 4 | a0001c0002t0006g0126a0001c0002t0006g0135a0001c0002t0006g0196others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+5174T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265338 | ||||||
| chr1:211265399
|
A | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.223+5235A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265399 | ||||||
| chr1:211265441
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.223+5277G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265441 | ||||||
| chr1:211265444
|
G | A | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+5280G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265444 | ||||||
| chr1:211265545
|
C | G | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+5381C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265545 | ||||||
| chr1:211265580
|
G | A | 63 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(60): Show | 70 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.223+5416G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265580 | ||||||
| chr1:211265602
|
C | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 52 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.223+5438C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265602 | ||||||
| chr1:211265651
|
G | A | 5 | a0001c0001t0003g0234a0001c0001t0003g0244a0001c0001t0003g0245others(2): Show | 5 | HG00597.hp1 NA18747.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+5487G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265651 | ||||||
| chr1:211265679
|
A | G | 4 | a0001c0002t0006g0126a0001c0002t0006g0135a0001c0002t0006g0196others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+5515A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265679 | ||||||
| chr1:211265697
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+5533G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265697 | ||||||
| chr1:211265810
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.224-5422A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265810 | ||||||
| chr1:211265827
|
TA | T | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-5401delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211265827 | |||||
| chr1:211265981
|
G | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-5251G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265981 | ||||||
| chr1:211266020
|
T | C | 1 | a0001c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.224-5212T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266020 | ||||||
| chr1:211266040
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.224-5192G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266040 | ||||||
| chr1:211266108
|
T | G | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-5124T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266108 | ||||||
| chr1:211266185
|
G | A | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-5047G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266185 | ||||||
| chr1:211266229
|
A | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.224-5003A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266229 | ||||||
| chr1:211266475
|
C | T | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.224-4757C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266475 | ||||||
| chr1:211266503
|
A | G | 2 | a0001c0004t0001g0298a0001c0004t0001g0299 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.224-4729A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266503 | ||||||
| chr1:211266537
|
A | C | 1 | a0001c0001t0002g0185 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.224-4695A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266537 | ||||||
| chr1:211266745
|
C | G | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.224-4487C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266745 | ||||||
| chr1:211266841
|
A | G | 1 | a0001c0002t0001g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.224-4391A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266841 | ||||||
| chr1:211267047
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.224-4185A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267047 | ||||||
| chr1:211267120
|
T | C | 1 | a0001c0002t0006g0196 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.224-4112T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267120 | ||||||
| chr1:211267277
|
C | A | 1 | a0001c0001t0002g0092 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.224-3955C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267277 | ||||||
| chr1:211267501
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.224-3731C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267501 | ||||||
| chr1:211267692
|
G | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.224-3540G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267692 | ||||||
| chr1:211267739
|
A | G | 3 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0013g0146 | 3 | HG00741.hp2 HG01069.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.224-3493A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267739 | ||||||
| chr1:211267812
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.224-3420C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267812 | ||||||
| chr1:211267924
|
A | T | 1 | a0001c0001t0011g0077 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.224-3308A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267924 | ||||||
| chr1:211268240
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0156 | 2 | HG00642.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.224-2992G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268240 | ||||||
| chr1:211268258
|
A | G | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.224-2974A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268258 | ||||||
| chr1:211268342
|
A | G | 52 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0024others(49): Show | 54 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.224-2890A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268342 | ||||||
| chr1:211268355
|
A | C | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-2877A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268355 | ||||||
| chr1:211268369
|
CT | C | 16 | a0001c0001t0001g0223a0001c0001t0003g0014a0001c0001t0003g0235others(13): Show | 17 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.224-2836delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268369 | |||||
| chr1:211268369
|
CTTTT | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(44): Show | 51 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.224-2839_224-2836d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268369 | |||||
| chr1:211268369
|
CTTTTT | C | 25 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0028others(22): Show | 25 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.224-2840_224-2836d others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268369 | |||||
| chr1:211268369
|
CTTTTTT | C | 182 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(179): Show | 193 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.224-2841_224-2836d others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268369 | |||||
| chr1:211268390
|
T | C | 65 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(62): Show | 69 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.224-2842T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268390 | ||||||
| chr1:211268456
|
C | G | 2 | a0001c0001t0002g0121a0001c0001t0002g0191 | 2 | NA18978.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.224-2776C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268456 | ||||||
| chr1:211268505
|
G | A | 1 | a0001c0001t0002g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.224-2727G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268505 | ||||||
| chr1:211268540
|
C | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.224-2692C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268540 | ||||||
| chr1:211268605
|
G | A | 1 | a0001c0002t0001g0222 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.224-2627G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268605 | ||||||
| chr1:211268607
|
C | T | 2 | a0001c0004t0001g0298a0001c0004t0001g0299 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.224-2625C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268607 | ||||||
| chr1:211268626
|
C | G | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-2606C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268626 | ||||||
| chr1:211268744
|
G | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0035others(4): Show | 9 | HG01099.hp2 HG01192.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-2488G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268744 | ||||||
| chr1:211268844
|
A | G | 156 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 164 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(161): Show |
intron_variant | MODIFIER | c.224-2388A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268844 | ||||||
| chr1:211268853
|
TATAAC | T | 4 | a0001c0002t0006g0126a0001c0002t0006g0135a0001c0002t0006g0196others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-2375_224-2371d others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268853 | |||||
| chr1:211268860
|
TA | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-2371delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268860 | ||||||
| chr1:211269139
|
G | A | 26 | a0001c0001t0002g0081a0001c0001t0002g0087a0001c0001t0002g0088others(23): Show | 26 | HG00642.hp1 HG01081.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.224-2093G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269139 | ||||||
| chr1:211269148
|
G | GGT | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-2083_224-2082d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211269148 | |||||
| chr1:211269157
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.224-2075C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269157 | ||||||
| chr1:211269207
|
T | C | 5 | a0001c0001t0002g0079a0001c0001t0002g0093a0001c0001t0002g0094others(2): Show | 5 | HG02080.hp1 NA18952.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-2025T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269207 | ||||||
| chr1:211269241
|
A | G | 1 | a0001c0001t0009g0233 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.224-1991A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269241 | ||||||
| chr1:211269319
|
C | T | 79 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(76): Show | 82 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.224-1913C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269319 | ||||||
| chr1:211269372
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.224-1860C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269372 | ||||||
| chr1:211269638
|
T | C | 105 | a0001c0001t0001g0021a0001c0001t0002g0001a0001c0001t0002g0009others(102): Show | 112 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.224-1594T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269638 | ||||||
| chr1:211269761
|
CTAT | C | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.224-1469_224-1467d others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211269761 | |||||
| chr1:211269880
|
C | CTACTAGC others(234): Show |
1 | a0001c0001t0002g0122 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.224-1348_224-1347i others(243): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211269880 | |||||
| chr1:211269937
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.224-1295A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269937 | ||||||
| chr1:211270066
|
C | CT | 259 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 274 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(271): Show |
intron_variant | MODIFIER | c.224-1152dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270066 | |||||
| chr1:211270131
|
C | T | 1 | a0001c0002t0001g0212 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.224-1101C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270131 | ||||||
| chr1:211270211
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.224-1021C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270211 | ||||||
| chr1:211270212
|
G | A | 1 | a0001c0002t0001g0198 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.224-1020G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270212 | ||||||
| chr1:211270298
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.224-934G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270298 | ||||||
| chr1:211270317
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.224-915C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270317 | ||||||
| chr1:211270524
|
A | G | 1 | a0001c0001t0008g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.224-708A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270524 | ||||||
| chr1:211270548
|
C | CA | 232 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0027others(229): Show | 247 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(244): Show |
intron_variant | MODIFIER | c.224-672dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270548 | |||||
| chr1:211270548
|
C | CAA | 50 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(47): Show | 54 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.224-673_224-672dup others(2): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270548 | |||||
| chr1:211270606
|
A | G | 1 | a0001c0001t0001g0291 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.224-626A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270606 | ||||||
| chr1:211270689
|
C | CT | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-537dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270689 | |||||
| chr1:211270777
|
G | A | 1 | a0001c0001t0004g0277 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.224-455G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270777 | ||||||
| chr1:211270819
|
TTGC | T | 282 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(279): Show | 301 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.224-409_224-407del others(3): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270819 | |||||
| chr1:211271003
|
T | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.224-229T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271003 | ||||||
| chr1:211271040
|
G | A | 79 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(76): Show | 82 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.224-192G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271040 | ||||||
| chr1:211271100
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.224-132G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271100 | ||||||
| chr1:211271109
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.224-123G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271109 | ||||||
| chr1:211271135
|
G | A | 1 | a0001c0001t0002g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.224-97G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271135 | ||||||
| chr1:211271159
|
C | G | 1 | a0001c0001t0005g0018 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.224-73C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271159 | ||||||
| chr1:211271376
|
C | T | 4 | a0001c0002t0001g0083a0001c0002t0001g0142a0001c0002t0001g0210others(1): Show | 4 | HG01257.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+67C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211271376 | ||||||
| chr1:211271948
|
G | A | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.301+639G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211271948 | ||||||
| chr1:211272122
|
G | A | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.301+813G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272122 | ||||||
| chr1:211272172
|
C | G | 1 | a0001c0001t0002g0182 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.301+863C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272172 | ||||||
| chr1:211272463
|
A | G | 52 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0024others(49): Show | 54 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.301+1154A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272463 | ||||||
| chr1:211272612
|
C | CT | 41 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0039others(38): Show | 47 | HG00609.hp2 HG00673.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.301+1330dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | |||||
| chr1:211272612
|
C | CTT | 27 | a0001c0001t0001g0028a0001c0001t0001g0082a0001c0001t0001g0144others(24): Show | 28 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.301+1329_301+1330d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | |||||
| chr1:211272612
|
C | CTTT | 36 | a0001c0001t0001g0016a0001c0001t0001g0260a0001c0001t0001g0267others(33): Show | 37 | HG01070.hp2 HG01884.hp1 HG02004.hp1 others(34): Show |
intron_variant | MODIFIER | c.301+1328_301+1330d others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | |||||
| chr1:211272612
|
C | CTTTT | 33 | a0001c0001t0001g0029a0001c0001t0001g0258a0001c0001t0001g0271others(30): Show | 33 | HG00642.hp1 HG01109.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.301+1327_301+1330d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | |||||
| chr1:211272612
|
C | CTTTTT | 42 | a0001c0001t0001g0021a0001c0001t0001g0272a0001c0001t0001g0290others(39): Show | 43 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.301+1326_301+1330d others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | |||||
| chr1:211272612
|
C | CTTTTTT | 58 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(55): Show | 65 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.301+1325_301+1330d others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | |||||
| chr1:211272612
|
C | CTTTTTTT | 15 | a0001c0001t0002g0011a0001c0001t0002g0026a0001c0001t0002g0069others(12): Show | 16 | HG00673.hp2 HG02523.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.301+1324_301+1330d others(9): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | |||||
| chr1:211272654
|
C | A | 1 | a0001c0002t0017g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301+1345C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272654 | ||||||
| chr1:211272683
|
G | A | 2 | a0001c0001t0007g0002a0001c0001t0007g0075 | 5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+1374G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272683 | ||||||
| chr1:211272771
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.302-1439G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272771 | ||||||
| chr1:211272864
|
G | A | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.302-1346G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272864 | ||||||
| chr1:211273096
|
G | C | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.302-1114G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211273096 | ||||||
| chr1:211273370
|
G | A | 73 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 77 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.302-840G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211273370 | ||||||
| chr1:211273612
|
A | G | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.302-598A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211273612 | ||||||
| chr1:211273635
|
C | T | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.302-575C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211273635 | ||||||
| chr1:211274058
|
C | G | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.302-152C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211274058 | ||||||
| chr1:211274060
|
C | G | 7 | a0001c0001t0002g0101a0001c0001t0002g0116a0001c0001t0002g0119others(4): Show | 7 | HG00597.hp2 HG00733.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.302-150C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211274060 | ||||||
| chr1:211274093
|
CT | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.302-107delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211274093 | |||||
| chr1:211274155
|
C | G | 2 | a0001c0001t0005g0004a0001c0001t0005g0074 | 4 | HG02486.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-55C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211274155 | ||||||
| chr1:211274283
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.354+21G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211274283 | ||||||
| chr1:211274778
|
A | G | 2 | a0001c0001t0003g0235a0001c0001t0003g0247 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.354+516A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211274778 | ||||||
| chr1:211275479
|
C | CA | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-777dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 211275479 | |||||
| chr1:211275521
|
A | G | 2 | a0001c0001t0002g0119a0001c0001t0012g0117 | 2 | HG00597.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.355-736A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211275521 | ||||||
| chr1:211275529
|
T | C | 13 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(10): Show | 14 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.355-728T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211275529 | ||||||
| chr1:211275805
|
A | ATTAC | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.355-452_355-451ins others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211275805 | ||||||
| chr1:211276109
|
A | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.355-148A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211276109 | ||||||
| chr1:211276655
|
A | G | 1 | a0001c0001t0002g0178 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.516+237A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276655 | ||||||
| chr1:211276815
|
C | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.516+397C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276815 | ||||||
| chr1:211276831
|
T | A | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.516+413T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276831 | ||||||
| chr1:211276852
|
C | T | 1 | a0001c0001t0003g0241 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.516+434C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276852 | ||||||
| chr1:211276958
|
C | T | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.516+540C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276958 | ||||||
| chr1:211277005
|
G | GA | 10 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0272others(7): Show | 10 | HG03491.hp2 HG03834.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.516+589dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 211277005 | |||||
| chr1:211277013
|
G | T | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.516+595G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277013 | ||||||
| chr1:211277022
|
G | T | 1 | a0001c0001t0004g0277 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.516+604G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277022 | ||||||
| chr1:211277073
|
G | A | 6 | a0001c0002t0006g0126a0001c0002t0006g0135a0001c0002t0006g0196others(3): Show | 6 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+655G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277073 | ||||||
| chr1:211277085
|
C | CA | 21 | a0001c0001t0001g0041a0001c0001t0002g0158a0001c0001t0003g0014others(18): Show | 22 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.516+678dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 211277085 | |||||
| chr1:211277089
|
A | G | 2 | a0001c0001t0007g0002a0001c0001t0007g0075 | 5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+671A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277089 | ||||||
| chr1:211277169
|
C | CT | 15 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(12): Show | 15 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.516+761dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 211277169 | |||||
| chr1:211277173
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.516+755T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277173 | ||||||
| chr1:211277716
|
A | T | 1 | a0001c0001t0004g0278 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.517-401A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277716 | ||||||
| chr1:211277920
|
T | G | 1 | a0001c0003t0001g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-197T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277920 | ||||||
| chr1:211278051
|
TATC | T | 79 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(76): Show | 82 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.517-61_517-59delTC others(1): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 211278051 | |||||
| chr1:211278516
|
G | T | 5 | a0001c0001t0002g0101a0001c0001t0002g0116a0001c0001t0002g0179others(2): Show | 5 | HG00733.hp2 HG01358.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.641+275G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278516 | ||||||
| chr1:211278672
|
A | G | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.641+431A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278672 | ||||||
| chr1:211278714
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.641+473G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278714 | ||||||
| chr1:211278788
|
TAA | T | 17 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(14): Show | 17 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.642-447_642-446del others(2): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 211278788 | |||||
| chr1:211278871
|
A | G | 1 | a0001c0002t0001g0084 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.642-367A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278871 | ||||||
| chr1:211278900
|
G | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(53): Show | 60 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.642-338G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278900 | ||||||
| chr1:211279004
|
T | G | 1 | a0001c0002t0001g0203 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.642-234T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211279004 | ||||||
| chr1:211279048
|
G | C | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.642-190G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211279048 | ||||||
| chr1:211279102
|
G | A | 56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(53): Show | 60 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.642-136G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211279102 | ||||||
| chr1:211279187
|
TA | T | 290 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(287): Show | 312 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.642-36delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 211279187 | |||||
| chr1:211279187
|
TAA | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0035a0001c0001t0001g0064others(4): Show | 7 | HG02717.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.642-37_642-36delAA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 211279187 | |||||
| chr1:211279336
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.720+20G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279336 | ||||||
| chr1:211279386
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.720+70G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279386 | ||||||
| chr1:211279408
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.720+92G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279408 | ||||||
| chr1:211279503
|
A | G | 79 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(76): Show | 82 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.720+187A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279503 | ||||||
| chr1:211279796
|
G | A | 23 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(20): Show | 27 | HG00609.hp1 HG01099.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.720+480G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279796 | ||||||
| chr1:211279884
|
G | C | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.720+568G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279884 | ||||||
| chr1:211280466
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.720+1150A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280466 | ||||||
| chr1:211280563
|
A | G | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1247A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280563 | ||||||
| chr1:211280572
|
C | G | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.720+1256C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280572 | ||||||
| chr1:211280591
|
C | G | 2 | a0001c0001t0002g0149a0001c0001t0002g0165 | 2 | HG01433.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.720+1275C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280591 | ||||||
| chr1:211280639
|
A | G | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.720+1323A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280639 | ||||||
| chr1:211280653
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.720+1337A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280653 | ||||||
| chr1:211280706
|
G | A | 1 | a0001c0001t0005g0005 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.720+1390G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280706 | ||||||
| chr1:211280971
|
C | T | 1 | a0001c0001t0004g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.720+1655C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280971 | ||||||
| chr1:211280984
|
C | CA | 19 | a0001c0001t0002g0025a0001c0001t0002g0153a0001c0001t0002g0184others(16): Show | 20 | HG00099.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.720+1685dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211280984 | |||||
| chr1:211280984
|
C | CAA | 95 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(92): Show | 102 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.720+1684_720+1685d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211280984 | |||||
| chr1:211280984
|
CA | C | 72 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(69): Show | 80 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.720+1685delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211280984 | |||||
| chr1:211281001
|
AG | A | 27 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(24): Show | 28 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.720+1687delG | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211281001 | |||||
| chr1:211281034
|
C | T | 9 | a0001c0001t0004g0261a0001c0001t0004g0262a0001c0001t0004g0264others(6): Show | 9 | HG01109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.720+1718C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211281034 | ||||||
| chr1:211281331
|
G | C | 2 | a0001c0004t0001g0298a0001c0004t0001g0299 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.720+2015G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211281331 | ||||||
| chr1:211281560
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.720+2244G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211281560 | ||||||
| chr1:211281673
|
A | G | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.720+2357A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211281673 | ||||||
| chr1:211282017
|
G | A | 2 | a0001c0001t0002g0188a0001c0001t0002g0193 | 2 | HG01081.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.720+2701G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282017 | ||||||
| chr1:211282286
|
CA | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 52 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.720+2972delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211282286 | |||||
| chr1:211282454
|
A | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0251others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+3138A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282454 | ||||||
| chr1:211282503
|
G | GT | 11 | a0001c0001t0001g0020a0001c0001t0001g0041a0001c0001t0001g0052others(8): Show | 12 | HG00642.hp1 HG00741.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+3203dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211282503 | |||||
| chr1:211282589
|
C | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.720+3273C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282589 | ||||||
| chr1:211282660
|
G | A | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.720+3344G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282660 | ||||||
| chr1:211282943
|
T | C | 1 | a0001c0002t0017g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.720+3627T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282943 | ||||||
| chr1:211283119
|
T | C | 1 | a0001c0001t0005g0259 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.720+3803T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283119 | ||||||
| chr1:211283263
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(2): Show | 5 | HG01243.hp1 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+3947G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283263 | ||||||
| chr1:211283604
|
A | G | 1 | a0001c0002t0001g0198 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.720+4288A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283604 | ||||||
| chr1:211283637
|
C | T | 4 | a0001c0001t0005g0005a0001c0001t0005g0018a0001c0001t0005g0259others(1): Show | 5 | HG00741.hp1 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+4321C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283637 | ||||||
| chr1:211283638
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.720+4322G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283638 | ||||||
| chr1:211283690
|
G | A | 8 | a0001c0001t0001g0144a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+4374G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283690 | ||||||
| chr1:211283741
|
T | C | 118 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(115): Show | 125 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.720+4425T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283741 | ||||||
| chr1:211283785
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.720+4469A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283785 | ||||||
| chr1:211283812
|
A | AT | 79 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(76): Show | 82 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.720+4510dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211283812 | |||||
| chr1:211283916
|
C | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.720+4600C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283916 | ||||||
| chr1:211284064
|
A | T | 1 | a0001c0001t0001g0292 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.720+4748A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284064 | ||||||
| chr1:211284210
|
C | T | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+4894C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284210 | ||||||
| chr1:211284376
|
G | A | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.721-4802G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284376 | ||||||
| chr1:211284479
|
G | C | 27 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(24): Show | 28 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.721-4699G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284479 | ||||||
| chr1:211284502
|
C | CTTTA | 127 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(124): Show | 137 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.721-4654_721-4651d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284502 | |||||
| chr1:211284502
|
C | CTTTATTT others(1): Show |
16 | a0001c0001t0001g0021a0001c0001t0001g0050a0001c0001t0001g0053others(13): Show | 16 | HG00558.hp1 HG00642.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.721-4658_721-4651d others(10): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284502 | |||||
| chr1:211284502
|
C | CTTTATTT others(5): Show |
1 | a0001c0001t0002g0090 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.721-4662_721-4651d others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284502 | |||||
| chr1:211284520
|
TTATTTAT others(1): Show |
T | 81 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(78): Show | 84 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(81): Show |
intron_variant | MODIFIER | c.721-4650_721-4643d others(10): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284520 | |||||
| chr1:211284524
|
TTATG | T | 20 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(17): Show | 21 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.721-4650_721-4647d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284524 | |||||
| chr1:211284528
|
G | T | 187 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(184): Show | 199 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.721-4650G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284528 | ||||||
| chr1:211284548
|
G | A | 1 | a0001c0003t0001g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.721-4630G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284548 | ||||||
| chr1:211284574
|
GT | G | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-4603delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284574 | ||||||
| chr1:211284794
|
T | C | 110 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 116 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.721-4384T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284794 | ||||||
| chr1:211285058
|
T | C | 2 | a0001c0001t0002g0086a0001c0001t0002g0151 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.721-4120T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285058 | ||||||
| chr1:211285154
|
C | G | 1 | a0001c0001t0002g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.721-4024C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285154 | ||||||
| chr1:211285196
|
T | A | 1 | a0001c0001t0001g0041 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.721-3982T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285196 | ||||||
| chr1:211285297
|
A | C | 1 | a0001c0001t0001g0040 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.721-3881A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285297 | ||||||
| chr1:211285465
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.721-3713G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285465 | ||||||
| chr1:211285839
|
G | A | 1 | a0001c0001t0003g0242 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.721-3339G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285839 | ||||||
| chr1:211285892
|
T | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.721-3286T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285892 | ||||||
| chr1:211286032
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.721-3146C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286032 | ||||||
| chr1:211286215
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.721-2963C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286215 | ||||||
| chr1:211286312
|
CT | C | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.721-2851delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211286312 | |||||
| chr1:211286338
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.721-2840C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286338 | ||||||
| chr1:211286368
|
C | T | 2 | a0001c0001t0002g0185a0001c0001t0015g0177 | 2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.721-2810C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286368 | ||||||
| chr1:211286452
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.721-2726C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286452 | ||||||
| chr1:211286523
|
G | A | 2 | a0001c0004t0001g0298a0001c0004t0001g0299 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.721-2655G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286523 | ||||||
| chr1:211286549
|
C | T | 2 | a0001c0001t0007g0002a0001c0001t0007g0075 | 5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-2629C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286549 | ||||||
| chr1:211286610
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.721-2568A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286610 | ||||||
| chr1:211286625
|
T | C | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-2553T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286625 | ||||||
| chr1:211286687
|
G | A | 2 | a0001c0001t0002g0121a0001c0001t0002g0191 | 2 | NA18978.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.721-2491G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286687 | ||||||
| chr1:211286820
|
A | G | 4 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0109others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-2358A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286820 | ||||||
| chr1:211286924
|
C | G | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-2254C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286924 | ||||||
| chr1:211287255
|
T | C | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1923T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287255 | ||||||
| chr1:211287487
|
A | G | 2 | a0001c0002t0006g0202a0001c0002t0006g0213 | 2 | HG02698.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.721-1691A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287487 | ||||||
| chr1:211287490
|
A | G | 2 | a0001c0001t0003g0235a0001c0001t0003g0247 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.721-1688A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287490 | ||||||
| chr1:211287538
|
G | A | 2 | a0001c0001t0007g0002a0001c0001t0007g0075 | 5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-1640G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287538 | ||||||
| chr1:211287552
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.721-1626G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287552 | ||||||
| chr1:211287659
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.721-1519T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287659 | ||||||
| chr1:211287750
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.721-1428G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287750 | ||||||
| chr1:211287832
|
C | A | 6 | a0001c0002t0001g0013a0001c0002t0001g0024a0001c0002t0001g0085others(3): Show | 7 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.721-1346C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287832 | ||||||
| chr1:211287885
|
C | T | 1 | a0001c0001t0002g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.721-1293C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287885 | ||||||
| chr1:211288008
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.721-1170G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288008 | ||||||
| chr1:211288166
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.721-1012C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288166 | ||||||
| chr1:211288218
|
A | T | 52 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0024others(49): Show | 54 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.721-960A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288218 | ||||||
| chr1:211288312
|
A | G | 2 | a0001c0001t0001g0035a0001c0001t0001g0064 | 2 | NA18977.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.721-866A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288312 | ||||||
| chr1:211288348
|
C | T | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.721-830C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288348 | ||||||
| chr1:211288390
|
G | A | 52 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0024others(49): Show | 54 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.721-788G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288390 | ||||||
| chr1:211288463
|
C | A | 1 | a0001c0001t0002g0096 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.721-715C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288463 | ||||||
| chr1:211288496
|
T | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.721-682T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288496 | ||||||
| chr1:211288513
|
A | AAATT | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.721-665_721-664ins others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288513 | ||||||
| chr1:211288519
|
A | G | 104 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0009others(101): Show | 111 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.721-659A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288519 | ||||||
| chr1:211288637
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.721-541A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288637 | ||||||
| chr1:211288685
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.721-493T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288685 | ||||||
| chr1:211288727
|
C | G | 1 | a0001c0001t0016g0236 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.721-451C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288727 | ||||||
| chr1:211288775
|
G | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.721-403G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288775 | ||||||
| chr1:211288778
|
C | A | 280 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 296 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(293): Show |
intron_variant | MODIFIER | c.721-400C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288778 | ||||||
| chr1:211288883
|
A | G | 2 | a0001c0002t0006g0202a0001c0002t0006g0213 | 2 | HG02698.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.721-295A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288883 | ||||||
| chr1:211289088
|
G | T | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.721-90G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211289088 | ||||||
| chr1:211289562
|
G | C | 1 | a0001c0001t0002g0092 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.939+166G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289562 | ||||||
| chr1:211289628
|
C | A | 1 | a0001c0001t0002g0081 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.939+232C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289628 | ||||||
| chr1:211289714
|
A | G | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+318A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289714 | ||||||
| chr1:211289765
|
GGTT | G | 49 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(46): Show | 53 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.939+375_939+377del others(3): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211289765 | |||||
| chr1:211289822
|
A | G | 2 | a0001c0004t0001g0298a0001c0004t0001g0299 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.939+426A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289822 | ||||||
| chr1:211289950
|
C | A | 1 | a0001c0001t0001g0273 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.939+554C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289950 | ||||||
| chr1:211289982
|
A | G | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+586A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289982 | ||||||
| chr1:211290070
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0228 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.939+674G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290070 | ||||||
| chr1:211290363
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(44): Show | 51 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.939+967G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290363 | ||||||
| chr1:211290393
|
A | C | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.939+997A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290393 | ||||||
| chr1:211290473
|
C | T | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.939+1077C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290473 | ||||||
| chr1:211290487
|
G | C | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.939+1091G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290487 | ||||||
| chr1:211290561
|
A | T | 2 | a0001c0001t0002g0119a0001c0001t0012g0117 | 2 | HG00597.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.939+1165A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290561 | ||||||
| chr1:211290672
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0271 | 2 | NA18941.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.939+1276G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290672 | ||||||
| chr1:211290773
|
C | T | 79 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(76): Show | 82 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.939+1377C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290773 | ||||||
| chr1:211290972
|
G | GT | 56 | a0001c0001t0001g0021a0001c0001t0001g0252a0001c0001t0002g0108others(53): Show | 58 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.939+1586dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211290972 | |||||
| chr1:211291714
|
ACATAGGC | A | 55 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 59 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.939+2321_939+2327d others(9): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211291714 | |||||
| chr1:211291737
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.939+2341T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211291737 | ||||||
| chr1:211291789
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0036a0001c0001t0001g0049others(2): Show | 5 | HG00558.hp1 HG02132.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+2393C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211291789 | ||||||
| chr1:211291968
|
A | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 59 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.939+2572A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211291968 | ||||||
| chr1:211292057
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.939+2661G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292057 | ||||||
| chr1:211292192
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.939+2796T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292192 | ||||||
| chr1:211292208
|
T | C | 6 | a0001c0002t0006g0126a0001c0002t0006g0135a0001c0002t0006g0196others(3): Show | 6 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+2812T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292208 | ||||||
| chr1:211292237
|
G | A | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.939+2841G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292237 | ||||||
| chr1:211292275
|
A | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.939+2879A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292275 | ||||||
| chr1:211292281
|
G | A | 104 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0009others(101): Show | 111 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.939+2885G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292281 | ||||||
| chr1:211292303
|
C | T | 1 | a0001c0003t0001g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.939+2907C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292303 | ||||||
| chr1:211292620
|
T | A | 104 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0009others(101): Show | 111 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.940-3056T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292620 | ||||||
| chr1:211292785
|
G | A | 1 | a0001c0003t0001g0141 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.940-2891G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292785 | ||||||
| chr1:211292921
|
TA | T | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.940-2751delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211292921 | |||||
| chr1:211293017
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.940-2659G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293017 | ||||||
| chr1:211293033
|
G | A | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.940-2643G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293033 | ||||||
| chr1:211293086
|
A | AAAAT | 124 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 135 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.940-2559_940-2556d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | |||||
| chr1:211293086
|
A | AAAATAAA others(1): Show |
51 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0057others(48): Show | 51 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.940-2563_940-2556d others(10): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | |||||
| chr1:211293086
|
A | AAAATAAA others(5): Show |
66 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0144others(63): Show | 69 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(66): Show |
intron_variant | MODIFIER | c.940-2567_940-2556d others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | |||||
| chr1:211293086
|
A | AAAATAAA others(9): Show |
18 | a0001c0001t0001g0027a0001c0001t0001g0224a0001c0001t0001g0251others(15): Show | 19 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.940-2571_940-2556d others(18): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | |||||
| chr1:211293086
|
AAAATAAA others(5): Show |
A | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.940-2567_940-2556d others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | |||||
| chr1:211293118
|
T | TAAATAAA others(10): Show |
3 | a0001c0001t0001g0029a0001c0001t0001g0267a0001c0001t0001g0273 | 3 | HG01192.hp1 HG04115.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.940-2556_940-2555i others(19): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293118 | |||||
| chr1:211293386
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0271 | 2 | HG00558.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.940-2290C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293386 | ||||||
| chr1:211293419
|
A | G | 290 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.940-2257A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293419 | ||||||
| chr1:211293444
|
A | G | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.940-2232A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293444 | ||||||
| chr1:211293561
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.940-2115C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293561 | ||||||
| chr1:211293644
|
G | A | 104 | a0001c0001t0001g0020a0001c0001t0002g0001a0001c0001t0002g0009others(101): Show | 111 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.940-2032G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293644 | ||||||
| chr1:211293739
|
A | G | 3 | a0001c0001t0002g0164a0001c0001t0002g0187a0001c0001t0002g0249 | 3 | NA18980.hp2 NA19078.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.940-1937A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293739 | ||||||
| chr1:211293801
|
T | G | 1 | a0001c0001t0002g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.940-1875T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293801 | ||||||
| chr1:211293933
|
A | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.940-1743A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293933 | ||||||
| chr1:211293968
|
G | A | 1 | a0001c0002t0001g0024 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.940-1708G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293968 | ||||||
| chr1:211293994
|
T | C | 1 | a0001c0002t0001g0198 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.940-1682T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293994 | ||||||
| chr1:211294145
|
T | G | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-1531T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294145 | ||||||
| chr1:211294260
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0294 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.940-1416T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294260 | ||||||
| chr1:211294312
|
T | C | 290 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.940-1364T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294312 | ||||||
| chr1:211294367
|
G | T | 1 | a0001c0001t0001g0290 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.940-1309G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294367 | ||||||
| chr1:211294510
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.940-1166C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294510 | ||||||
| chr1:211294567
|
GACTTTTC others(35): Show |
G | 1 | a0001c0001t0001g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.940-1108_940-1067d others(44): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294567 | ||||||
| chr1:211294586
|
C | CT | 109 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 116 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.940-1069dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211294586 | |||||
| chr1:211294586
|
CT | C | 152 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0027others(149): Show | 164 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.940-1069delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211294586 | |||||
| chr1:211294590
|
T | C | 13 | a0001c0001t0002g0100a0001c0001t0004g0015a0001c0001t0004g0261others(10): Show | 14 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.940-1086T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294590 | ||||||
| chr1:211294618
|
C | T | 11 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(8): Show | 11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.940-1058C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294618 | ||||||
| chr1:211294624
|
G | C | 290 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.940-1052G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294624 | ||||||
| chr1:211294628
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 115 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.940-1048C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294628 | ||||||
| chr1:211294676
|
A | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.940-1000A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294676 | ||||||
| chr1:211294691
|
G | A | 3 | a0001c0001t0002g0025a0001c0001t0002g0149a0001c0001t0002g0165 | 3 | HG01433.hp1 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.940-985G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294691 | ||||||
| chr1:211294832
|
G | A | 2 | a0001c0001t0003g0235a0001c0001t0003g0247 | 2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.940-844G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294832 | ||||||
| chr1:211295002
|
T | C | 1 | a0001c0002t0001g0216 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.940-674T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295002 | ||||||
| chr1:211295041
|
C | A | 1 | a0001c0002t0001g0217 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.940-635C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295041 | ||||||
| chr1:211295042
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-634T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295042 | ||||||
| chr1:211295066
|
T | TG | 16 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0028others(13): Show | 16 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.940-610_940-609ins others(1): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295066 | ||||||
| chr1:211295066
|
T | TTG | 121 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(118): Show | 128 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.940-609_940-608ins others(2): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211295066 | |||||
| chr1:211295066
|
T | TTTG | 132 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0031others(129): Show | 141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.940-609_940-608ins others(3): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211295066 | |||||
| chr1:211295066
|
T | TTTTG | 15 | a0001c0001t0001g0021a0001c0001t0001g0290a0001c0001t0001g0292others(12): Show | 15 | HG00642.hp1 HG00741.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.940-609_940-608ins others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211295066 | |||||
| chr1:211295431
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.940-245A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295431 | ||||||
| chr1:211295468
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.940-208G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295468 | ||||||
| chr1:211295512
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.940-164A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295512 | ||||||
| chr1:211295616
|
G | A | 1 | a0001c0002t0001g0204 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.940-60G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295616 | ||||||
| chr1:211295906
|
A | G | 2 | a0001c0002t0001g0083a0001c0002t0001g0211 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1017+153A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211295906 | ||||||
| chr1:211296155
|
A | C | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1017+402A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296155 | ||||||
| chr1:211296155
|
A | T | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1017+402A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296155 | ||||||
| chr1:211296208
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1017+455T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296208 | ||||||
| chr1:211296338
|
TA | T | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1017+587delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211296338 | |||||
| chr1:211296746
|
A | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1017+993A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296746 | ||||||
| chr1:211296847
|
T | C | 1 | a0001c0004t0001g0299 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1017+1094T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296847 | ||||||
| chr1:211297152
|
A | G | 2 | a0001c0002t0001g0139a0001c0002t0001g0203 | 2 | NA18939.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1017+1399A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297152 | ||||||
| chr1:211297175
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0251others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+1422G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297175 | ||||||
| chr1:211297296
|
A | C | 1 | a0001c0001t0002g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1017+1543A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297296 | ||||||
| chr1:211297385
|
C | G | 41 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(38): Show | 43 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.1017+1632C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297385 | ||||||
| chr1:211297391
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1017+1638G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297391 | ||||||
| chr1:211297485
|
C | T | 27 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(24): Show | 28 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.1017+1732C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297485 | ||||||
| chr1:211297494
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1017+1741G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297494 | ||||||
| chr1:211297516
|
G | A | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1017+1763G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297516 | ||||||
| chr1:211298163
|
A | T | 6 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0254others(3): Show | 6 | HG02280.hp1 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+2410A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211298163 | ||||||
| chr1:211298256
|
G | A | 2 | a0001c0001t0004g0015a0001c0001t0004g0279 | 3 | HG01884.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1017+2503G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211298256 | ||||||
| chr1:211298331
|
AAG | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0251others(1): Show | 4 | HG01243.hp1 HG02257.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+2581_1017+258 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211298331 | |||||
| chr1:211298354
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1017+2601A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211298354 | ||||||
| chr1:211298778
|
G | A | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1017+3025G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211298778 | ||||||
| chr1:211299001
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1017+3248C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299001 | ||||||
| chr1:211299044
|
G | A | 1 | a0001c0002t0006g0213 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1017+3291G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299044 | ||||||
| chr1:211299067
|
A | G | 1 | a0001c0001t0004g0278 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1017+3314A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299067 | ||||||
| chr1:211299087
|
AGTACAGA others(5): Show |
A | 1 | a0001c0001t0001g0020 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1017+3338_1017+334 others(16): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211299087 | |||||
| chr1:211299201
|
G | A | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1017+3448G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299201 | ||||||
| chr1:211299206
|
T | C | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1017+3453T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299206 | ||||||
| chr1:211299389
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1017+3636G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299389 | ||||||
| chr1:211299440
|
G | A | 1 | a0001c0002t0001g0198 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1017+3687G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299440 | ||||||
| chr1:211299637
|
CG | C | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1017+3888delG | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211299637 | |||||
| chr1:211299663
|
G | A | 1 | a0001c0001t0002g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1017+3910G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299663 | ||||||
| chr1:211299794
|
G | A | 7 | a0001c0001t0001g0007a0001c0001t0001g0033a0001c0001t0001g0034others(4): Show | 8 | HG00609.hp1 HG02083.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.1017+4041G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299794 | ||||||
| chr1:211299865
|
T | G | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1017+4112T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299865 | ||||||
| chr1:211300039
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1018-4044C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300039 | ||||||
| chr1:211300071
|
C | CT | 110 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0032others(107): Show | 118 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1018-3994dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211300071 | |||||
| chr1:211300071
|
C | CTT | 26 | a0001c0001t0001g0273a0001c0001t0002g0023a0001c0001t0002g0079others(23): Show | 27 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1018-3995_1018-399 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211300071 | |||||
| chr1:211300071
|
CT | C | 3 | a0001c0001t0007g0002a0001c0001t0007g0075a0001c0002t0001g0207 | 6 | HG01070.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018-3994delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211300071 | |||||
| chr1:211300075
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0294 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1018-4008T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300075 | ||||||
| chr1:211300362
|
G | A | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1018-3721G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300362 | ||||||
| chr1:211300398
|
C | G | 1 | a0001c0001t0002g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1018-3685C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300398 | ||||||
| chr1:211300402
|
T | C | 2 | a0001c0001t0007g0002a0001c0001t0007g0075 | 5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-3681T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300402 | ||||||
| chr1:211300406
|
G | C | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1018-3677G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300406 | ||||||
| chr1:211300507
|
T | G | 1 | a0001c0001t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1018-3576T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300507 | ||||||
| chr1:211300799
|
A | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1018-3284A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300799 | ||||||
| chr1:211300906
|
A | G | 287 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(284): Show | 303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1018-3177A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300906 | ||||||
| chr1:211300908
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(100): Show | 110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1018-3175G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300908 | ||||||
| chr1:211300913
|
C | CGT | 5 | a0001c0001t0001g0028a0001c0001t0002g0088a0001c0001t0002g0188others(2): Show | 5 | HG00642.hp1 HG01081.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-3168_1018-316 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211300913 | |||||
| chr1:211300917
|
C | T | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1018-3166C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300917 | ||||||
| chr1:211300979
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1018-3104C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300979 | ||||||
| chr1:211301106
|
A | T | 4 | a0001c0001t0001g0021a0001c0001t0002g0099a0001c0001t0002g0230others(1): Show | 4 | HG03195.hp1 HG03453.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-2977A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301106 | ||||||
| chr1:211301161
|
T | C | 2 | a0001c0001t0002g0188a0001c0001t0002g0193 | 2 | HG01081.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1018-2922T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301161 | ||||||
| chr1:211301381
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1018-2702G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301381 | ||||||
| chr1:211301413
|
T | G | 1 | a0001c0001t0001g0258 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1018-2670T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301413 | ||||||
| chr1:211301521
|
G | A | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1018-2562G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301521 | ||||||
| chr1:211301552
|
T | C | 1 | a0001c0001t0010g0103 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1018-2531T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301552 | ||||||
| chr1:211301700
|
G | A | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1018-2383G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301700 | ||||||
| chr1:211301903
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1018-2180T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301903 | ||||||
| chr1:211301991
|
A | C | 27 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(24): Show | 28 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.1018-2092A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301991 | ||||||
| chr1:211302043
|
T | A | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1018-2040T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302043 | ||||||
| chr1:211302094
|
A | G | 2 | a0001c0002t0001g0138a0001c0002t0001g0217 | 2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1018-1989A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302094 | ||||||
| chr1:211302192
|
T | C | 1 | a0001c0001t0001g0055 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1018-1891T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302192 | ||||||
| chr1:211302461
|
A | G | 56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(53): Show | 60 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1018-1622A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302461 | ||||||
| chr1:211302584
|
C | T | 2 | a0001c0001t0001g0082a0001c0002t0001g0131 | 2 | HG02559.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1018-1499C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302584 | ||||||
| chr1:211302679
|
C | T | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1018-1404C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302679 | ||||||
| chr1:211302911
|
C | A | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1018-1172C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302911 | ||||||
| chr1:211303081
|
C | G | 139 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 146 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.1018-1002C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303081 | ||||||
| chr1:211303147
|
C | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(53): Show | 60 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1018-936C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303147 | ||||||
| chr1:211303625
|
GA | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1018-451delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211303625 | |||||
| chr1:211303721
|
T | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1018-362T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303721 | ||||||
| chr1:211303730
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1018-353G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303730 | ||||||
| chr1:211303895
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1018-188A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303895 | ||||||
| chr1:211304057
|
T | G | 4 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0109others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-26T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211304057 | ||||||
| chr1:211304400
|
C | T | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1075+260C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304400 | ||||||
| chr1:211304679
|
C | T | 4 | a0001c0002t0006g0126a0001c0002t0006g0135a0001c0002t0006g0196others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+539C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304679 | ||||||
| chr1:211304708
|
C | A | 290 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(287): Show | 309 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.1075+568C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304708 | ||||||
| chr1:211304857
|
A | G | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+717A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304857 | ||||||
| chr1:211304981
|
T | C | 4 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0109others(1): Show | 4 | HG01109.hp1 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+841T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304981 | ||||||
| chr1:211305116
|
G | A | 2 | a0001c0001t0002g0099a0001c0001t0002g0230 | 2 | HG04184.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1075+976G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305116 | ||||||
| chr1:211305232
|
A | G | 1 | a0001c0001t0002g0175 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1075+1092A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305232 | ||||||
| chr1:211305233
|
T | C | 1 | a0001c0001t0001g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1075+1093T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305233 | ||||||
| chr1:211305788
|
G | A | 1 | a0001c0001t0004g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1075+1648G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305788 | ||||||
| chr1:211305809
|
A | C | 1 | a0001c0001t0001g0287 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1075+1669A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305809 | ||||||
| chr1:211305914
|
G | C | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1075+1774G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305914 | ||||||
| chr1:211305989
|
G | A | 20 | a0001c0001t0002g0182a0001c0001t0003g0014a0001c0001t0003g0234others(17): Show | 21 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1075+1849G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305989 | ||||||
| chr1:211306209
|
C | G | 1 | a0001c0001t0002g0096 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1075+2069C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306209 | ||||||
| chr1:211306211
|
G | C | 64 | a0001c0001t0001g0269a0001c0001t0001g0271a0001c0001t0001g0272others(61): Show | 66 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(63): Show |
intron_variant | MODIFIER | c.1075+2071G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306211 | ||||||
| chr1:211306233
|
T | A | 117 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0082others(114): Show | 124 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1075+2093T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306233 | ||||||
| chr1:211306484
|
A | G | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1075+2344A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306484 | ||||||
| chr1:211306842
|
G | T | 1 | a0001c0001t0002g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1075+2702G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306842 | ||||||
| chr1:211307074
|
T | C | 3 | a0001c0001t0001g0272a0001c0001t0001g0283a0001c0001t0001g0297 | 3 | NA18956.hp1 NA18969.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1075+2934T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307074 | ||||||
| chr1:211307142
|
T | G | 1 | a0001c0001t0002g0195 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1075+3002T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307142 | ||||||
| chr1:211307241
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1075+3101C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307241 | ||||||
| chr1:211307296
|
C | T | 2 | a0001c0004t0001g0298a0001c0004t0001g0299 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1075+3156C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307296 | ||||||
| chr1:211307486
|
AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1075+3361_1075+337 others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211307486 | |||||
| chr1:211307490
|
A | AAGAATTT others(6): Show |
11 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(8): Show | 12 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+3350_1075+335 others(17): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307490 | ||||||
| chr1:211307490
|
A | AGAATTTA others(5): Show |
275 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(272): Show | 290 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.1075+3360_1075+336 others(16): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211307490 | |||||
| chr1:211307529
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1075+3389A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307529 | ||||||
| chr1:211307562
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1075+3422T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307562 | ||||||
| chr1:211307783
|
A | T | 1 | a0001c0002t0001g0198 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1075+3643A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307783 | ||||||
| chr1:211307791
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1075+3651C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307791 | ||||||
| chr1:211308001
|
C | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0055others(1): Show | 4 | NA18990.hp1 NA19002.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+3861C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308001 | ||||||
| chr1:211308015
|
AAGAT | A | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1075+3879_1075+388 others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308015 | |||||
| chr1:211308182
|
A | AGACACCA others(27): Show |
1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1075+4044_1075+407 others(38): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308182 | |||||
| chr1:211308187
|
C | T | 6 | a0001c0001t0002g0106a0001c0001t0002g0111a0001c0001t0002g0112others(3): Show | 6 | HG00558.hp2 HG04228.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075+4047C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308187 | ||||||
| chr1:211308332
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1075+4192T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308332 | ||||||
| chr1:211308498
|
T | C | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1076-4222T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308498 | ||||||
| chr1:211308636
|
T | C | 20 | a0001c0001t0002g0182a0001c0001t0003g0014a0001c0001t0003g0234others(17): Show | 21 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1076-4084T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308636 | ||||||
| chr1:211308660
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1076-4060T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308660 | ||||||
| chr1:211308662
|
TTTTTTTT others(4): Show |
T | 29 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(26): Show | 30 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1076-4036_1076-402 others(15): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308662 | |||||
| chr1:211308663
|
TTTTTTTT others(3): Show |
T | 4 | a0001c0001t0004g0262a0001c0001t0004g0278a0001c0001t0004g0279others(1): Show | 4 | HG02257.hp2 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076-4047_1076-403 others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308663 | |||||
| chr1:211308664
|
TTTTTTTT others(2): Show |
T | 8 | a0001c0001t0001g0021a0001c0001t0004g0015a0001c0001t0004g0261others(5): Show | 9 | HG01884.hp2 HG02451.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1076-4047_1076-403 others(13): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308664 | |||||
| chr1:211308665
|
TTTTTTTT others(12): Show |
T | 1 | a0001c0001t0001g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1076-4047_1076-402 others(23): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308665 | |||||
| chr1:211308670
|
TTTGTTTT others(7): Show |
T | 1 | a0001c0001t0002g0172 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1076-4047_1076-403 others(18): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308670 | |||||
| chr1:211308671
|
TTGTTTTT others(6): Show |
T | 57 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0011others(54): Show | 63 | HG00099.hp1 HG00408.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.1076-4047_1076-403 others(17): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308671 | |||||
| chr1:211308672
|
TGTTTTTT others(5): Show |
T | 42 | a0001c0001t0002g0010a0001c0001t0002g0026a0001c0001t0002g0079others(39): Show | 43 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1076-4047_1076-403 others(16): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308672 | ||||||
| chr1:211308673
|
G | GT | 10 | a0001c0001t0001g0260a0001c0001t0003g0014a0001c0001t0003g0234others(7): Show | 11 | HG00099.hp2 HG00738.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1076-4037dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308673 | |||||
| chr1:211308673
|
G | GTT | 9 | a0001c0001t0002g0182a0001c0001t0003g0240a0001c0001t0003g0241others(6): Show | 9 | HG00597.hp1 HG02165.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076-4038_1076-403 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308673 | |||||
| chr1:211308673
|
G | T | 9 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0251others(6): Show | 9 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076-4047G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308673 | ||||||
| chr1:211308674
|
TTTTTTTT others(3): Show |
T | 2 | a0001c0002t0001g0140a0001c0002t0001g0222 | 2 | HG01928.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1076-4036_1076-402 others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308674 | |||||
| chr1:211308680
|
T | G | 1 | a0001c0001t0008g0274 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1076-4040T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308680 | ||||||
| chr1:211308681
|
T | G | 3 | a0001c0001t0008g0275a0001c0001t0008g0276a0001c0001t0008g0296 | 3 | HG02922.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1076-4039T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308681 | ||||||
| chr1:211308683
|
T | TTG | 45 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0024others(42): Show | 47 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.1076-4037_1076-403 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308683 | ||||||
| chr1:211308684
|
G | T | 156 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 164 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.1076-4036G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308684 | ||||||
| chr1:211308687
|
T | TG | 54 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(51): Show | 58 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1076-4033_1076-403 others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308687 | ||||||
| chr1:211308692
|
T | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0255 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1076-4028T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308692 | ||||||
| chr1:211308694
|
T | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0255 | 2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1076-4026T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308694 | ||||||
| chr1:211308694
|
T | TG | 5 | a0001c0001t0001g0252a0001c0001t0001g0254a0001c0001t0001g0257others(2): Show | 5 | HG02280.hp1 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076-4026_1076-402 others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308694 | ||||||
| chr1:211308695
|
T | G | 1 | a0001c0002t0001g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1076-4025T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308695 | ||||||
| chr1:211308696
|
T | G | 5 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0254others(2): Show | 5 | HG02280.hp1 HG02970.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076-4024T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308696 | ||||||
| chr1:211308698
|
T | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0082a0001c0001t0001g0250others(5): Show | 8 | HG01243.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1076-4022T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308698 | ||||||
| chr1:211308698
|
T | TTTTTTTT others(7): Show |
1 | a0001c0001t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1076-4021_1076-402 others(18): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308698 | |||||
| chr1:211308716
|
AT | A | 286 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(283): Show | 302 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.1076-3991delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308716 | |||||
| chr1:211308717
|
T | C | 2 | a0001c0001t0002g0167a0001c0001t0002g0173 | 2 | NA18982.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1076-4003T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308717 | ||||||
| chr1:211308718
|
T | C | 100 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(97): Show | 107 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1076-4002T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308718 | ||||||
| chr1:211308768
|
G | A | 12 | a0001c0001t0004g0015a0001c0001t0004g0261a0001c0001t0004g0262others(9): Show | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1076-3952G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308768 | ||||||
| chr1:211308769
|
TG | T | 102 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(99): Show | 109 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1076-3950delG | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308769 | ||||||
| chr1:211308952
|
T | A | 20 | a0001c0001t0002g0182a0001c0001t0003g0014a0001c0001t0003g0234others(17): Show | 21 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1076-3768T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308952 | ||||||
| chr1:211308955
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1076-3765G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308955 | ||||||
| chr1:211308971
|
T | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1076-3749T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308971 | ||||||
| chr1:211309086
|
T | TA | 33 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0056others(30): Show | 37 | HG01070.hp1 HG01070.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1076-3614dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211309086 | |||||
| chr1:211309086
|
T | TAA | 138 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(135): Show | 146 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.1076-3615_1076-361 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211309086 | |||||
| chr1:211309086
|
T | TAAA | 109 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0030others(106): Show | 116 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1076-3616_1076-361 others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211309086 | |||||
| chr1:211309227
|
T | C | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1076-3493T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309227 | ||||||
| chr1:211309277
|
A | G | 26 | a0001c0001t0001g0016a0001c0001t0001g0029a0001c0001t0001g0258others(23): Show | 27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1076-3443A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309277 | ||||||
| chr1:211309404
|
ATGACTTA others(6): Show |
A | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3314_1076-330 others(17): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211309404 | |||||
| chr1:211309444
|
C | T | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3276C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309444 | ||||||
| chr1:211309457
|
A | C | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3263A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309457 | ||||||
| chr1:211309458
|
T | A | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3262T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309458 | ||||||
| chr1:211309459
|
A | G | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3261A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309459 | ||||||
| chr1:211309461
|
G | A | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3259G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309461 | ||||||
| chr1:211309468
|
T | G | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3252T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309468 | ||||||
| chr1:211309470
|
TGCCAGCA others(4): Show |
T | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3249_1076-323 others(15): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309470 | ||||||
| chr1:211309482
|
A | T | 1 | a0001c0001t0003g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3238A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309482 | ||||||
| chr1:211309563
|
C | G | 102 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(99): Show | 109 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1076-3157C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309563 | ||||||
| chr1:211309744
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1076-2976G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309744 | ||||||
| chr1:211309845
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0251a0001c0001t0001g0253 | 3 | HG01243.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1076-2875G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309845 | ||||||
| chr1:211309915
|
A | T | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1076-2805A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309915 | ||||||
| chr1:211309966
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1076-2754C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309966 | ||||||
| chr1:211309978
|
T | C | 288 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(285): Show | 304 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(301): Show |
intron_variant | MODIFIER | c.1076-2742T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309978 | ||||||
| chr1:211310026
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1076-2694C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310026 | ||||||
| chr1:211310310
|
G | T | 19 | a0001c0001t0003g0014a0001c0001t0003g0234a0001c0001t0003g0235others(16): Show | 20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1076-2410G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310310 | ||||||
| chr1:211310516
|
G | T | 4 | a0001c0001t0008g0274a0001c0001t0008g0275a0001c0001t0008g0276others(1): Show | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-2204G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310516 | ||||||
| chr1:211310608
|
C | G | 1 | a0001c0001t0003g0242 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1076-2112C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310608 | ||||||
| chr1:211310629
|
C | G | 1 | a0001c0001t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1076-2091C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310629 | ||||||
| chr1:211310672
|
A | G | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | NA18990.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1076-2048A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310672 | ||||||
| chr1:211310758
|
A | T | 54 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0024others(51): Show | 56 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1076-1962A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310758 | ||||||
| chr1:211310918
|
T | A | 7 | a0001c0001t0004g0261a0001c0001t0004g0262a0001c0001t0004g0264others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076-1802T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310918 | ||||||
| chr1:211311718
|
A | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 116 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.1076-1002A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211311718 | ||||||
| chr1:211311770
|
A | G | 1 | a0001c0001t0003g0239 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1076-950A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211311770 | ||||||
| chr1:211311851
|
A | G | 1 | a0001c0001t0005g0078 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1076-869A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211311851 | ||||||
| chr1:211311885
|
A | C | 2 | a0001c0001t0001g0021a0001c0001t0018g0022 | 2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1076-835A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211311885 | ||||||
| chr1:211312159
|
T | G | 1 | a0001c0001t0002g0107 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1076-561T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211312159 | ||||||
| chr1:211312183
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076-537G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211312183 | ||||||
| chr1:211312195
|
T | G | 1 | a0001c0001t0002g0181 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1076-525T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211312195 | ||||||
| chr1:211312529
|
G | A | 1 | a0001c0001t0004g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1076-191G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211312529 | ||||||
| chr1:211313236
|
C | T | 1 | a0001c0001t0004g0263 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1318-188C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 11/11 | chr1 | 211313236 | ||||||
| chr1:211313365
|
T | C | 1 | a0001c0001t0003g0238 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1318-59T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 11/11 | chr1 | 211313365 |